-
1
-
-
84859169877
-
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
-
Barretina J, Caponigro G, Stransky N, Venkatesan K, Margolin AA, Kim S, Wilson Lehár, CJ J, Kryukov GV, Sonkin D, Reddy A, Liu M, Murray L, Berger MF, Monahan JE, Morais P, et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature. 2012; 483: 603-607.
-
(2012)
Nature.
, vol.483
, pp. 603-607
-
-
Barretina, J.1
Caponigro, G.2
Stransky, N.3
Venkatesan, K.4
Margolin, A.A.5
Kim, S.6
Wilson, C.J.7
Lehár, J.8
Kryukov, G.V.9
Sonkin, D.10
Reddy, A.11
Liu, M.12
Murray, L.13
Berger, M.F.14
Monahan, J.E.15
Morais, P.16
-
2
-
-
84859187259
-
Systematic identification of genomic markers of drug sensitivity in cancer cells
-
Garnett MJ, Edelman EJ, Heidorn SJ, Greenman CD, Dastur A, Lau KW, Greninger P, Thompson IR, Luo X, Soares J, Liu Q, Iorio F, Surdez D, Chen L, Milano RJ, Bignell GR, et al. Systematic identification of genomic markers of drug sensitivity in cancer cells. Nature. 2012; 483: 570-575.
-
(2012)
Nature.
, vol.483
, pp. 570-575
-
-
Garnett, M.J.1
Edelman, E.J.2
Heidorn, S.J.3
Greenman, C.D.4
Dastur, A.5
Lau, K.W.6
Greninger, P.7
Thompson, I.R.8
Luo, X.9
Soares, J.10
Liu, Q.11
Iorio, F.12
Surdez, D.13
Chen, L.14
Milano, R.J.15
Bignell, G.R.16
-
3
-
-
79959712087
-
Ras/Raf/MEK/ ERK and PI3K/PTEN/Akt/mTOR Inhibitors: Rationale and Importance to Inhibiting These Pathways in Human Health
-
Chappell WH, Steelman LS, Long JM, Kempf RC, Abrams SL, Franklin RA, Bäsecke J, Stivala F, Donia M, Fagone P, Malaponte G, Mazzarino MC, Nicoletti F, Libra M, Maksimovic-Ivanic D, Mijatovic S, et al. Ras/Raf/MEK/ ERK and PI3K/PTEN/Akt/mTOR Inhibitors: Rationale and Importance to Inhibiting These Pathways in Human Health. Oncotarget. 2011; 2: 135-164.
-
(2011)
Oncotarget.
, vol.2
, pp. 135-164
-
-
Chappell, W.H.1
Steelman, L.S.2
Long, J.M.3
Kempf, R.C.4
Abrams, S.L.5
Franklin, R.A.6
Bäsecke, J.7
Stivala, F.8
Donia, M.9
Fagone, P.10
Malaponte, G.11
Mazzarino, M.C.12
Nicoletti, F.13
Libra, M.14
Maksimovic-Ivanic, D.15
Mijatovic, S.16
-
4
-
-
79960237399
-
Therapeutic resistance resulting from mutations in Raf/MEK/ERK and PI3K/ PTEN/Akt/mTOR signaling pathways
-
McCubrey JA, Steelman LS, Kempf CR, Chappell W, Abrams SL, Stivala F, Malaponte G, Nicoletti F, Libra M, Bäsecke J, Maksimovic-Ivanic D, Mijatovic S, Montalto G, Cervello M, Cocco L, Martelli AM. Therapeutic resistance resulting from mutations in Raf/MEK/ERK and PI3K/ PTEN/Akt/mTOR signaling pathways. J Cell Physiol. 2011; 226: 2762-2781.
-
(2011)
J Cell Physiol.
, vol.226
, pp. 2762-2781
-
-
Mccubrey, J.A.1
Steelman, L.S.2
Kempf, C.R.3
Chappell, W.4
Abrams, S.L.5
Stivala, F.6
Malaponte, G.7
Nicoletti, F.8
Libra, M.9
Bäsecke, J.10
Maksimovic-Ivanic, D.11
Mijatovic, S.12
Montalto, G.13
Cervello, M.14
Cocco, L.15
Martelli, A.M.16
-
5
-
-
31144453233
-
BRAF mutation predicts sensitivity to MEK inhibition
-
Solit DB, Garraway LA, Pratilas CA, Sawai A, Getz G, Basso A, Ye Q, Lobo JM, She Y, Osman I, Golub TR, Sebolt-Leopold J, Sellers WR, Rosen N. BRAF mutation predicts sensitivity to MEK inhibition. Nature. 2006; 439: 358-362.
-
(2006)
Nature.
, vol.439
, pp. 358-362
-
-
Solit, D.B.1
Garraway, L.A.2
Pratilas, C.A.3
Sawai, A.4
Getz, G.5
Basso, A.6
Ye, Q.7
Lobo, J.M.8
She, Y.9
Osman, I.10
Golub, T.R.11
Sebolt-Leopold, J.12
Sellers, W.R.13
Rosen, N.14
-
6
-
-
79960271775
-
Targeting the translational apparatus to improve leukemia therapy: roles of the PI3K/PTEN/Akt/ mTOR pathway
-
Martelli AM, Evangelisti C, Chappell W, Abrams SL, Bäsecke J, Stivala F, Donia M, Fagone P, Nicoletti F, Libra M, Ruvolo V, Ruvolo P, Kempf CR, Steelman LS, McCubrey JA. Targeting the translational apparatus to improve leukemia therapy: roles of the PI3K/PTEN/Akt/ mTOR pathway. Leukemia. 2011; 25: 1064-1079.
-
(2011)
Leukemia.
, vol.25
, pp. 1064-1079
-
-
Martelli, A.M.1
Evangelisti, C.2
Chappell, W.3
Abrams, S.L.4
Bäsecke, J.5
Stivala, F.6
Donia, M.7
Fagone, P.8
Nicoletti, F.9
Libra, M.10
Ruvolo, V.11
Ruvolo, P.12
Kempf, C.R.13
Steelman, L.S.14
McCubrey, J.A.15
-
7
-
-
84865805718
-
Dual Inhibitors of phosphatidylinositol 3-kinase and mammalian target of rapamycin: a novel therapeutic strategy for acute leukemia treatment?
-
Martelli AM, Chiarini F, Evangelisti C, Cappellini A, Buontempo F, Bressanin D, Fini M, McCubrey JA. Dual Inhibitors of phosphatidylinositol 3-kinase and mammalian target of rapamycin: a novel therapeutic strategy for acute leukemia treatment? Oncotarget. 2012; 3: 371-394.
-
(2012)
Oncotarget.
, vol.3
, pp. 371-394
-
-
Martelli, A.M.1
Chiarini, F.2
Evangelisti, C.3
Cappellini, A.4
Buontempo, F.5
Bressanin, D.6
Fini, M.7
Mccubrey, J.A.8
-
8
-
-
84862558416
-
Targeting the liver kinase B1/AMPdependent kinase pathway as a therapeutic strategy for hematological malignancies
-
Martelli AM, Chiarini F, Evangelisti C, Ognibene A, Bressanin D, Billi AM, Manzoli L, Cappellini A, McCubrey JA. Targeting the liver kinase B1/AMPdependent kinase pathway as a therapeutic strategy for hematological malignancies. Expert Opinion Therapeutic Targets. 2012; 16: 729-742
-
(2012)
Expert Opinion Therapeutic Targets.
, vol.16
, pp. 729-742
-
-
Martelli, A.M.1
Chiarini, F.2
Evangelisti, C.3
Ognibene, A.4
Bressanin, D.5
Billi, A.M.6
Manzoli, L.7
Cappellini, A.8
Mccubrey, J.A.9
-
9
-
-
77952864300
-
Emerging MEK inhibitors
-
McCubrey JA, Steelman LS, Abrams SL, Chappell WH, Russo S, Ove R, Milella M, Tafuri A, Lunghi P, Bonati A, Stivala F, Nicoletti F, Libra M, Martelli AM, Montalto G, Cervello M. Emerging MEK inhibitors. Exp Opin Emerging Drugs. 2010; 15: 203-223.
-
(2010)
Exp Opin Emerging Drugs.
, vol.15
, pp. 203-223
-
-
Mccubrey, J.A.1
Steelman, L.S.2
Abrams, S.L.3
Chappell, W.H.4
Russo, S.5
Ove, R.6
Milella, M.7
Tafuri, A.8
Lunghi, P.9
Bonati, A.10
Stivala, F.11
Nicoletti, F.12
Libra, M.13
Martelli, A.M.14
Montalto, G.15
Cervello, M.16
-
10
-
-
79961173138
-
Roles of the Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR pathways in controlling growth and sensitivity to therapy-implications for cancer and aging
-
Steelman LS, Chappell WH, Abrams SL, Kempf RC, Long J, Laidler P, Mijatovic S, Maksimovic-Ivanic D, Stivala F, Mazzarino MC, Donia M, Fagone P, Malaponte G, Nicoletti F, Libra M, Milella M, et al. Roles of the Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR pathways in controlling growth and sensitivity to therapy-implications for cancer and aging. Aging. 2011; 3: 192-222.
-
(2011)
Aging.
, vol.3
, pp. 192-222
-
-
Steelman, L.S.1
Chappell, W.H.2
Abrams, S.L.3
Kempf, R.C.4
Long, J.5
Laidler, P.6
Mijatovic, S.7
Maksimovic-Ivanic, D.8
Stivala, F.9
Mazzarino, M.C.10
Donia, M.11
Fagone, P.12
Malaponte, G.13
Nicoletti, F.14
Libra, M.15
Milella, M.16
-
11
-
-
84864558037
-
Targeted therapy for hepatocellular carcinoma: novel agents on the horizon
-
Cervello M, McCubrey JA, Cusimano A, Lampiasi N, Azzolina A, Montalto G. Targeted therapy for hepatocellular carcinoma: novel agents on the horizon. Oncotarget. 2012; 3: 236-260.
-
(2012)
Oncotarget.
, vol.3
, pp. 236-260
-
-
Cervello, M.1
Mccubrey, J.A.2
Cusimano, A.3
Lampiasi, N.4
Azzolina, A.5
Montalto, G.6
-
12
-
-
68849110551
-
Sorafenib therapy in advanced hepatocellular carcinoma: the SHARP trial
-
Rimassa L, Santoro A. Sorafenib therapy in advanced hepatocellular carcinoma: the SHARP trial. Expert Rev Anticancer Ther. 2009; 9: 739-745.
-
(2009)
Expert Rev Anticancer Ther.
, vol.9
, pp. 739-745
-
-
Rimassa, L.1
Santoro, A.2
-
13
-
-
33846781365
-
Targeted inhibition of the extracellular signal-regulated kinases kinase pathway with AZD-6244 (ARRY-142886) in the treatment of hepatocellular carcinoma
-
Huynh H, Soo KC, Chow PK, Tran E. Targeted inhibition of the extracellular signal-regulated kinases kinase pathway with AZD-6244 (ARRY-142886) in the treatment of hepatocellular carcinoma. Mol Cancer Ther. 2007; 6: 138-146.
-
(2007)
Mol Cancer Ther.
, vol.6
, pp. 138-146
-
-
Huynh, H.1
Soo, K.C.2
Chow, P.K.3
Tran, E.4
-
14
-
-
79953234255
-
Resistance to MEK inhibitors: should we co-target upstream?
-
Poulikakos PI, Solit DB. Resistance to MEK inhibitors: should we co-target upstream? Sci Signal. 2011; 4: pe16.
-
(2011)
Sci Signal
, vol.4
, pp. 16
-
-
Poulikakos, P.I.1
Solit, D.B.2
-
15
-
-
4944249117
-
BAY 43-9006 Exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis
-
Wilhelm SM, Carter C, Tang LY, Wilkie D, McNabola A, Rong H, Chen C, Zhang X, Vincent P, McHugh M, Cao Y, Shujath J, Gawlak S, Eveleigh D, Rowley B, Liu L, et al. BAY 43-9006 Exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis. Cancer Research. 2004; 64: 7099-7109.
-
(2004)
Cancer Research.
, vol.64
, pp. 7099-7109
-
-
Wilhelm, S.M.1
Carter, C.2
Tang, L.Y.3
Wilkie, D.4
McNabola, A.5
Rong, H.6
Chen, C.7
Zhang, X.8
Vincent, P.9
Mchugh, M.10
Cao, Y.11
Shujath, J.12
Gawlak, S.13
Eveleigh, D.14
Rowley, B.15
Liu, L.16
-
16
-
-
79958016793
-
Antiangiogenic agents in advanced gastrointestinal malignancies: past, present and a novel future
-
Mulder K, Koski S, Scarfe A, Chu Q, King K, Spratlin J. Antiangiogenic agents in advanced gastrointestinal malignancies: past, present and a novel future. Oncotarget. 2010; 1: 515-529.
-
(2010)
Oncotarget.
, vol.1
, pp. 515-529
-
-
Mulder, K.1
Koski, S.2
Scarfe, A.3
Chu, Q.4
King, K.5
Spratlin, J.6
-
17
-
-
84864561983
-
Molecular mechanisms of sorafenib action in liver cancer cells
-
Cervello M, Bachvarov D, Lampiasi N, Cusimano A, Azzolina A, McCubrey JA, Montalto G. Molecular mechanisms of sorafenib action in liver cancer cells. Cell Cycle. 2012; 11: 2843-2855.
-
(2012)
Cell Cycle.
, vol.11
, pp. 2843-2855
-
-
Cervello, M.1
Bachvarov, D.2
Lampiasi, N.3
Cusimano, A.4
Azzolina, A.5
McCubrey, J.A.6
Montalto, G.7
-
18
-
-
58149328950
-
CRAF inhibition induces apoptosis in melanoma cells with non-V600E BRAF mutations
-
Smalley KS, Xiao M, Villanueva J, Nguyen TK, Flaherty KT, Letrero R, Van Belle P, Elder DE, Wang Y, Nathanson KL, Herlyn M. CRAF inhibition induces apoptosis in melanoma cells with non-V600E BRAF mutations. Oncogene. 2009; 28: 85-94.
-
(2009)
Oncogene.
, vol.28
, pp. 85-94
-
-
Smalley, K.S.1
Xiao, M.2
Villanueva, J.3
Nguyen, T.K.4
Flaherty, K.T.5
Letrero, R.6
Van Belle, P.7
Elder, D.E.8
Wang, Y.9
Nathanson, K.L.10
Herlyn, M.11
-
19
-
-
77956030786
-
Inhibition of mutated, activated BRAF in metastatic melanoma
-
Flaherty KT, Puzanov I, Kim KB, Ribas A, McArthur GA, Sosman JA, O'Dwyer PJ, Lee RJ, Grippo JF, Nolop K, Chapman PB. Inhibition of mutated, activated BRAF in metastatic melanoma. N Engl J Med. 2010; 363: 809-819.
-
(2010)
N Engl J Med.
, vol.363
, pp. 809-819
-
-
Flaherty, K.T.1
Puzanov, I.2
Kim, K.B.3
Ribas, A.4
McArthur, G.A.5
Sosman, J.A.6
O'Dwyer, P.J.7
Lee, R.J.8
Grippo, J.F.9
Nolop, K.10
Chapman, P.B.11
-
20
-
-
79959795786
-
BRIM-3 Study Group
-
Chapman PB, Hauschild A, Robert C, Haanen JB, Ascierto P, Larkin J, Dummer R, Garbe C, Testori A, Maio M, Hogg D, Lorigan P, Lebbe C, Jouary T, Schadendorf D, Ribas A, et al. BRIM-3 Study Group. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011; 364: 2507-2516.
-
(2011)
Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med.
, vol.364
, pp. 2507-2516
-
-
Chapman, P.B.1
Hauschild, A.2
Robert, C.3
Haanen, J.B.4
Ascierto, P.5
Larkin, J.6
Dummer, R.7
Garbe, C.8
Testori, A.9
Maio, M.10
Hogg, D.11
Lorigan, P.12
Lebbe, C.13
Jouary, T.14
Schadendorf, D.15
Ribas, A.16
-
21
-
-
79952453763
-
Melanoma cells show a heterogeneous range of sensitivity to ionizing radiation and are radiosensitized by inhibition of B-RAF with PLX-4032
-
Sambade MJ, Peters EC, Thomas NE, Kaufmann WK, Kimple RJ, Shields JM. Melanoma cells show a heterogeneous range of sensitivity to ionizing radiation and are radiosensitized by inhibition of B-RAF with PLX-4032. Radiother Oncol. 2011; 98: 394-399.
-
(2011)
Radiother Oncol.
, vol.98
, pp. 394-399
-
-
Sambade, M.J.1
Peters, E.C.2
Thomas, N.E.3
Kaufmann, W.K.4
Kimple, R.J.5
Shields, J.M.6
-
22
-
-
77956513286
-
Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma
-
Bollag G, Hirth P, Tsai J, Zhang J, Ibrahim PN, Cho H, Spevak W, Zhang C, Zhang Y, Habets G, Burton EA, Wong B, Tsang G, West BL, Powell B, Shellooe R, et al. Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma. Nature. 2010; 467: 596-599.
-
(2010)
Nature.
, vol.467
, pp. 596-599
-
-
Bollag, G.1
Hirth, P.2
Tsai, J.3
Zhang, J.4
Ibrahim, P.N.5
Cho, H.6
Spevak, W.7
Zhang, C.8
Zhang, Y.9
Habets, G.10
Burton, E.A.11
Wong, B.12
Tsang, G.13
West, B.L.14
Powell, B.15
Shellooe, R.16
-
23
-
-
79959293462
-
BRAF mutations in hairy-cell leukemia
-
Tiacci E, Trifonov V, Schiavoni G, Holmes A, Kern W, Martelli MP, Pucciarini A, Bigerna B, Pacini R, Wells VA, Sportoletti P, Pettirossi V, Mannucci R, Elliott O, Liso A, Ambrosetti A, et al. "BRAF mutations in hairy-cell leukemia". N Engl J Med. 2011; 364: 2305-2315.
-
(2011)
N Engl J Med.
, vol.364
, pp. 2305-2315
-
-
Tiacci, E.1
Trifonov, V.2
Schiavoni, G.3
Holmes, A.4
Kern, W.5
Martelli, M.P.6
Pucciarini, A.7
Bigerna, B.8
Pacini, R.9
Wells, V.A.10
Sportoletti, P.11
Pettirossi, V.12
Mannucci, R.13
Elliott, O.14
Liso, A.15
Ambrosetti, A.16
-
24
-
-
84868628069
-
Mutations and deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/ mTOR cascades which alter therapy response
-
McCubrey JA, Steelman LS, Chappell WH, Abrams SL, Franklin RA, Montalto G, Cervello M, Nicoletti F, Fagone P, Malaponte G, Mazzarino MC, Candido S, Libra M, Bäsecke J, Milella M, Tafuri A, et al. Mutations and deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/ mTOR cascades which alter therapy response. Oncotarget. 2012; 3: 954-987.
-
(2012)
Oncotarget.
, vol.3
, pp. 954-987
-
-
Mccubrey, J.A.1
Steelman, L.S.2
Chappell, W.H.3
Abrams, S.L.4
Franklin, R.A.5
Montalto, G.6
Cervello, M.7
Nicoletti, F.8
Fagone, P.9
Malaponte, G.10
Mazzarino, M.C.11
Candido, S.12
Libra, M.13
Bäsecke, J.14
Milella, M.15
Tafuri, A.16
-
25
-
-
42949149240
-
Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity
-
Tsai J, Lee JT, Wang W, Zhang J, Cho H, Mamo S, Bremer R, Gillette S, Kong J, Haass NK, Sproesser K, Li L, Smalley KS, Fong D, Zhu YL, Marimuthu A, et al. Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc Natl Acad Sci USA. 2008; 105: 3041-3046.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 3041-3046
-
-
Tsai, J.1
Lee, J.T.2
Wang, W.3
Zhang, J.4
Cho, H.5
Mamo, S.6
Bremer, R.7
Gillette, S.8
Kong, J.9
Haass, N.K.10
Sproesser, K.11
Li, L.12
Smalley, K.S.13
Fong, D.14
Zhu, Y.L.15
Marimuthu, A.16
-
26
-
-
77955602211
-
Gatekeeper mutations mediate resistance to BRAF-targeted therapies
-
Whittaker S, Kirk R, Hayward R, Zambon A, Viros A, Cantarino N, Affolter A, Nourry A, Niculescu-Duvaz D, Springer C, Marais R. Gatekeeper mutations mediate resistance to BRAF-targeted therapies. Sci Transl Med. 2010; 2: 35ra41.
-
(2010)
Sci Transl Med.
, vol.2
-
-
Whittaker, S.1
Kirk, R.2
Hayward, R.3
Zambon, A.4
Viros, A.5
Cantarino, N.6
Affolter, A.7
Nourry, A.8
Niculescu-Duvaz, D.9
Springer, C.10
Marais, R.11
-
27
-
-
84861083983
-
Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial
-
Falchook GS, Long GV, Kurzrock R, Kim KB, Arkenau TH, Brown MP, Hamid O, Infante JR, Millward M, Pavlick AC, O'Day SJ, Blackman SC, Curtis CM, Lebowitz P, Ma B, Ouellet D, et al. Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet. 2012; 379: 1893-1901.
-
(2012)
Lancet.
, vol.379
, pp. 1893-1901
-
-
Falchook, G.S.1
Long, G.V.2
Kurzrock, R.3
Kim, K.B.4
Arkenau, T.H.5
Brown, M.P.6
Hamid, O.7
Infante, J.R.8
Millward, M.9
Pavlick, A.C.10
O'Day, S.J.11
Blackman, S.C.12
Curtis, C.M.13
Lebowitz, P.14
Ma, B.15
Ouellet, D.16
-
28
-
-
78049284316
-
A novel, selective, and efficacious nanomolar pyridopyrazinone inhibitor of V600EBRAF
-
Whittaker S, Ménard D, Kirk R, Ogilvie L, Hedley D, Zambon A, Lopes F, Preece N, Manne H, Rana S, Lambros M, Reis-Filho JS, Marais R, Springer CJ. A novel, selective, and efficacious nanomolar pyridopyrazinone inhibitor of V600EBRAF. Cancer Res. 2010; 70: 8036-8044.
-
(2010)
Cancer Res.
, vol.70
, pp. 8036-8044
-
-
Whittaker, S.1
Ménard, D.2
Kirk, R.3
Ogilvie, L.4
Hedley, D.5
Zambon, A.6
Lopes, F.7
Preece, N.8
Manne, H.9
Rana, S.10
Lambros, M.11
Reis-Filho, J.S.12
Marais, R.13
Springer, C.J.14
-
29
-
-
66149126085
-
Antitumor Efficacy of the Novel RAF Inhibitor GDC-0879 Is Predicted by BRAFV600E Mutational Status and Sustained Extracellular Signal-Regulated Kinase/Mitogen-Activated Protein Kinase Pathway Suppression
-
Hoeflich KP, Herter S, Tien J, Wong L, Berry L, Chan J, O'Brien C, Modrusan Z, Seshagiri S, Lackner M, Stern H, Choo E, Murray L, Friedman LS, Belvin M. Antitumor Efficacy of the Novel RAF Inhibitor GDC-0879 Is Predicted by BRAFV600E Mutational Status and Sustained Extracellular Signal-Regulated Kinase/Mitogen-Activated Protein Kinase Pathway Suppression. Cancer Research. 2009; 69: 3042-3051.
-
(2009)
Cancer Research.
, vol.69
, pp. 3042-3051
-
-
Hoeflich, K.P.1
Herter, S.2
Tien, J.3
Wong, L.4
Berry, L.5
Chan, J.6
O'Brien, C.7
Modrusan, Z.8
Seshagiri, S.9
Lackner, M.10
Stern, H.11
Choo, E.12
Murray, L.13
Friedman, L.S.14
Belvin, M.15
-
30
-
-
80155210220
-
The Raf kinase inhibitor PLX5568 slows cyst proliferation in rat polycystic kidney disease but promotes renal and hepatic fibrosis
-
Buchholz B, Klanke B, Schley G, Bollag G, Tsai J, Kroening S, Yoshihara D, Wallace DP, Kraenzlin B, Gretz N, Hirth P, Eckardt KU, Bernhardt WM. The Raf kinase inhibitor PLX5568 slows cyst proliferation in rat polycystic kidney disease but promotes renal and hepatic fibrosis. Nephrol Dial Transplant. 2011; 26: 3458-3465.
-
(2011)
Nephrol Dial Transplant.
, vol.26
, pp. 3458-3465
-
-
Buchholz, B.1
Klanke, B.2
Schley, G.3
Bollag, G.4
Tsai, J.5
Kroening, S.6
Yoshihara, D.7
Wallace, D.P.8
Kraenzlin, B.9
Gretz, N.10
Hirth, P.11
Eckardt, K.U.12
Bernhardt, W.M.13
-
31
-
-
79953201876
-
The novel Raf inhibitor Raf265 decreases Bcl-2 levels and confers TRAILsensitivity to neuroendocrine tumour cells
-
Zitzmann K, de Toni E, von Rüden J, Brand S, Göke B, Laubender RP, Auernhammer CJ. The novel Raf inhibitor Raf265 decreases Bcl-2 levels and confers TRAILsensitivity to neuroendocrine tumour cells. Endocr Relat Cancer. 2011; 18: 277-285.
-
(2011)
Endocr Relat Cancer.
, vol.18
, pp. 277-285
-
-
Zitzmann, K.1
de Toni, E.2
von Rüden, J.3
Brand, S.4
Göke, B.5
Laubender, R.P.6
Auernhammer, C.J.7
-
32
-
-
79954499886
-
Regorafenib (BAY 73-4506): a new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity
-
Wilhelm SM, Dumas J, Adnane L, Lynch M, Carter CA, Schütz G, Thierauch KH, Zopf D Regorafenib (BAY 73-4506): a new oral multikinase inhibitor of angiogenic, stromal and oncogenic receptor tyrosine kinases with potent preclinical antitumor activity. Int J Cancer. 2011; 129: 245-255.
-
(2011)
Int J Cancer.
, vol.129
, pp. 245-255
-
-
Wilhelm, S.M.1
Dumas, J.2
Adnane, L.3
Lynch, M.4
Carter, C.A.5
Schütz, G.6
Thierauch, K.H.7
Zopf, D.8
-
33
-
-
49649118852
-
Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma
-
Montagut C, Sharma SV, Shioda T, McDermott U, Ulman M, Ulkus LE, Dias-Santagata D, Stubbs H, Lee DY, Singh A, Drew L, Haber DA, Settleman J. Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma. Cancer Res. 2008; 68: 4853-4861.
-
(2008)
Cancer Res.
, vol.68
, pp. 4853-4861
-
-
Montagut, C.1
Sharma, S.V.2
Shioda, T.3
McDermott, U.4
Ulman, M.5
Ulkus, L.E.6
Dias-Santagata, D.7
Stubbs, H.8
Lee, D.Y.9
Singh, A.10
Drew, L.11
Haber, D.A.12
Settleman, J.13
-
34
-
-
68949106943
-
A phase I study of XL281, a selective oral RAF kinase inhibitor, in patients(Pts) with advanced solid tumors
-
Schwartz GK, Robertson S, Shen A, Wang E, Pace L, Dials H, Mendelson D, Shannon P, Gordon M. A phase I study of XL281, a selective oral RAF kinase inhibitor, in patients(Pts) with advanced solid tumors. J Clin Oncol. 2009; 27: 15s.
-
(2009)
J Clin Oncol.
, vol.27
-
-
Schwartz, G.K.1
Robertson, S.2
Shen, A.3
Wang, E.4
Pace, L.5
Dials, H.6
Mendelson, D.7
Shannon, P.8
Gordon, M.9
-
35
-
-
33744984843
-
Phase II placebo-controlled randomized discontinuation trial of sorafenib in patients with metastatic renal cell carcinoma
-
Ratain MJ, Eisen T, Stadler WM, Flaherty KT, Kaye SB, Rosner GL, Gore M, Desai AA, Patnaik A, Xiong HQ, Rowinsky E, Abbruzzese JL, Xia C, Simantov R, Schwartz B, O'Dwyer PJ. Phase II placebo-controlled randomized discontinuation trial of sorafenib in patients with metastatic renal cell carcinoma. J. Clin. Oncol. 2006; 24: 2505-2512.
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 2505-2512
-
-
Ratain, M.J.1
Eisen, T.2
Stadler, W.M.3
Flaherty, K.T.4
Kaye, S.B.5
Rosner, G.L.6
Gore, M.7
Desai, A.A.8
Patnaik, A.9
Xiong, H.Q.10
Rowinsky, E.11
Abbruzzese, J.L.12
Xia, C.13
Simantov, R.14
Schwartz, B.15
O'Dwyer, P.J.16
-
36
-
-
33748325763
-
Sorafenib in advanced melanoma: a Phase II randomised discontinuation trial analysis
-
Eisen T, Ahmad T, Flaherty KT, Gore M, Kaye S, Marais R, Gibbens I, Hackett S, James M, Schuchter LM, Nathanson KL, Xia C, Simantov R, Schwartz B, Poulin-Costello M, O'Dwyer PJ, et al. Sorafenib in advanced melanoma: a Phase II randomised discontinuation trial analysis. Br J Cancer. 2006; 95: 581-586.
-
(2006)
Br J Cancer.
, vol.95
, pp. 581-586
-
-
Eisen, T.1
Ahmad, T.2
Flaherty, K.T.3
Gore, M.4
Kaye, S.5
Marais, R.6
Gibbens, I.7
Hackett, S.8
James, M.9
Schuchter, L.M.10
Nathanson, K.L.11
Xia, C.12
Simantov, R.13
Schwartz, B.14
Poulin-Costello, M.15
O'Dwyer, P.J.16
-
37
-
-
33846148701
-
TARGET Study Group
-
Escudier B, Eisen T, Stadler WM, Szczylik C, Oudard S, Siebels M, Negrier S, Chevreau C, Solska E, Desai AA, Rolland F, Demkow T, Hutson TE, Gore M, Freeman S, Schwartz B, et al. TARGET Study Group. Sorafenib in advanced clear-cell renal-cell carcinoma. N Engl J Med. 2007; 356: 125-134.
-
(2007)
Sorafenib in advanced clear-cell renal-cell carcinoma. N Engl J Med.
, vol.356
, pp. 125-134
-
-
Escudier, B.1
Eisen, T.2
Stadler, W.M.3
Szczylik, C.4
Oudard, S.5
Siebels, M.6
Negrier, S.7
Chevreau, C.8
Solska, E.9
Desai, A.A.10
Rolland, F.11
Demkow, T.12
Hutson, T.E.13
Gore, M.14
Freeman, S.15
Schwartz, B.16
-
38
-
-
38049019119
-
Safety and anti-tumor activity of sorafenib (Nexavar) in combination with other anti-cancer agents: a review of clinical trials
-
Takimoto CH, Awada A. Safety and anti-tumor activity of sorafenib (Nexavar) in combination with other anti-cancer agents: a review of clinical trials. Cancer Chemother Pharmacol. 2008; 61: 535-548.
-
(2008)
Cancer Chemother Pharmacol.
, vol.61
, pp. 535-548
-
-
Takimoto, C.H.1
Awada, A.2
-
39
-
-
33748030422
-
Targeting mitogen-activated protein kinase/extracellular signal-regulated kinase kinase in the mutant (V600E) B-Raf signaling cascade effectively inhibits melanoma lung metastases
-
Sharma A, Tran MA, Liang S, Sharma AK, Amin S, Smith CD, Dong C, Robertson GP. Targeting mitogen-activated protein kinase/extracellular signal-regulated kinase kinase in the mutant (V600E) B-Raf signaling cascade effectively inhibits melanoma lung metastases. Cancer Res. 2006; 66: 8200-8209.
-
(2006)
Cancer Res.
, vol.66
, pp. 8200-8209
-
-
Sharma, A.1
Tran, M.A.2
Liang, S.3
Sharma, A.K.4
Amin, S.5
Smith, C.D.6
Dong, C.7
Robertson, G.P.8
-
40
-
-
79959795786
-
BRIM-3 Study Group
-
Chapman PB, Hauschild A, Robert C, Haanen JB, Ascierto P, Larkin J, Dummer R, Garbe C, Testori A, Maio M, Hogg D, Lorigan P, Lebbe C, Jouary T, Schadendorf D, Ribas A, et al. BRIM-3 Study Group. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011; 364: 2507-2516.
-
(2011)
Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med.
, vol.364
, pp. 2507-2516
-
-
Chapman, P.B.1
Hauschild, A.2
Robert, C.3
Haanen, J.B.4
Ascierto, P.5
Larkin, J.6
Dummer, R.7
Garbe, C.8
Testori, A.9
Maio, M.10
Hogg, D.11
Lorigan, P.12
Lebbe, C.13
Jouary, T.14
Schadendorf, D.15
Ribas, A.16
-
41
-
-
84863116743
-
Survival in BRAF V600- mutant advanced melanoma treated with vemurafenib
-
Sosman JA, Kim KB, Schuchter L, Gonzalez R, Pavlick AC, Weber JS, McArthur GA, Hutson TE, Moschos SJ, Flaherty KT, Hersey P, Kefford R, Lawrence D, Puzanov I, Lewis KD, Amaravadi RK, et al. Survival in BRAF V600- mutant advanced melanoma treated with vemurafenib. N Engl J Med. 2012; 366: 707-714.
-
(2012)
N Engl J Med.
, vol.366
, pp. 707-714
-
-
Sosman, J.A.1
Kim, K.B.2
Schuchter, L.3
Gonzalez, R.4
Pavlick, A.C.5
Weber, J.S.6
McArthur, G.A.7
Hutson, T.E.8
Moschos, S.J.9
Flaherty, K.T.10
Hersey, P.11
Kefford, R.12
Lawrence, D.13
Puzanov, I.14
Lewis, K.D.15
Amaravadi, R.K.16
-
42
-
-
77957350123
-
Phase I/II study of GSK2118436, a selective inhibitor of oncogenic mutant BRAF kinase, in patients with metastatic melanoma and other solid tumors
-
Kefford R, Arkenau H, Brown MP, Millward M, Infante JR, Long GV, Ouellet D, Curtis M, Lebowitz PF, Falchook GS. Phase I/II study of GSK2118436, a selective inhibitor of oncogenic mutant BRAF kinase, in patients with metastatic melanoma and other solid tumors. J Clin Oncol. 2010; 28:15s.
-
(2010)
J Clin Oncol.
, vol.28
-
-
Kefford, R.1
Arkenau, H.2
Brown, M.P.3
Millward, M.4
Infante, J.R.5
Long, G.V.6
Ouellet, D.7
Curtis, M.8
Lebowitz, P.F.9
Falchook, G.S.10
-
43
-
-
79953891558
-
Phase 1/2 study of GSK2118436, a selective inhibitor of V600 mutant (mut) BRAF kinase: evidence of activity in melanoma brain metastases (mets)
-
Long GV, Kefford RF, Carr PJA, Brown MP, Curtis M, Ma B, Lebowitz P, Kim KB, Kurzrock R, Flachook G. Phase 1/2 study of GSK2118436, a selective inhibitor of V600 mutant (mut) BRAF kinase: evidence of activity in melanoma brain metastases (mets). Annals of Oncology. 2010; 21: (Supplement 8: viii12).
-
(2010)
Annals of Oncology
, vol.21
, Issue.SUPPL. 8
, pp. 812
-
-
Long, G.V.1
Kefford, R.F.2
Carr, P.J.A.3
Brown, M.P.4
Curtis, M.5
Ma, B.6
Lebowitz, P.7
Kim, K.B.8
Kurzrock, R.9
Flachook, G.10
-
44
-
-
77949732073
-
RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF
-
Poulikakos PI, Zhang C, Bollag G, Shokat KM, Rosen N. RAF inhibitors transactivate RAF dimers and ERK signalling in cells with wild-type BRAF. Nature. 2010; 464: 427-430.
-
(2010)
Nature
, vol.464
, pp. 427-430
-
-
Poulikakos, P.I.1
Zhang, C.2
Bollag, G.3
Shokat, K.M.4
Rosen, N.5
-
45
-
-
78651418282
-
Mutant BRAF melanomas- dependence and resistance
-
Poulikakos PI, Rosen N. Mutant BRAF melanomas- dependence and resistance. Cancer Cell. 2011; 19: 11-15.
-
(2011)
Cancer Cell.
, vol.19
, pp. 11-15
-
-
Poulikakos, P.I.1
Rosen, N.2
-
46
-
-
77957089182
-
The RAF inhibitor PLX4032 inhibits ERK signaling and tumor cell proliferation in a V600E BRAF-selective manner
-
Joseph EW, Pratilas CA, Poulikakos PI, Tadi M, Wang W, Taylor BS, Halilovic E, Persaud Y, Xing F, Viale A, Tsai J, Chapman PB, Bollag G, Solit DB, Rosen N. The RAF inhibitor PLX4032 inhibits ERK signaling and tumor cell proliferation in a V600E BRAF-selective manner. Proc Natl Acad Sci U S A. 2010; 107: 14903-14908.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 14903-14908
-
-
Joseph, E.W.1
Pratilas, C.A.2
Poulikakos, P.I.3
Tadi, M.4
Wang, W.5
Taylor, B.S.6
Halilovic, E.7
Persaud, Y.8
Xing, F.9
Viale, A.10
Tsai, J.11
Chapman, P.B.12
Bollag, G.13
Solit, D.B.14
Rosen, N.15
-
47
-
-
74849109743
-
Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF
-
Heidorn SJ, Milagre C, Whittaker S, Nourry A, Niculescu-Duvas I, Dhomen N, Hussain J, Reis-Filho JS, Springer CJ, Pritchard C, Marais R. Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF. Cell. 2010; 140: 209-221.
-
(2010)
Cell
, vol.140
, pp. 209-221
-
-
Heidorn, S.J.1
Milagre, C.2
Whittaker, S.3
Nourry, A.4
Niculescu-Duvas, I.5
Dhomen, N.6
Hussain, J.7
Reis-Filho, J.S.8
Springer, C.J.9
Pritchard, C.10
Marais, R.11
-
48
-
-
84862908097
-
RAS mutations in cutaneous squamous-cell carcinomas in patients treated with BRAF inhibitors
-
Su F, Viros A, Milagre C, Trunzer K, Bollag G, Spleiss O, Reis-Filho JS, Kong X, Koya RC, Flaherty KT, Chapman PB, Kim MJ, Hayward R, Martin M, Yang H, Wang Q, et al. RAS mutations in cutaneous squamous-cell carcinomas in patients treated with BRAF inhibitors. N Engl J Med. 2012; 366: 207-215.
-
(2012)
N Engl J Med.
, vol.366
, pp. 207-215
-
-
Su, F.1
Viros, A.2
Milagre, C.3
Trunzer, K.4
Bollag, G.5
Spleiss, O.6
Reis-Filho, J.S.7
Kong, X.8
Koya, R.C.9
Flaherty, K.T.10
Chapman, P.B.11
Kim, M.J.12
Hayward, R.13
Martin, M.14
Yang, H.15
Wang, Q.16
-
49
-
-
84862908526
-
RAS mutations are associated with the development of cutaneous squamous cell tumors in patients treated with RAF inhibitors
-
Oberholzer PA, Kee D, Dziunycz P, Sucker A, Kamsukom N, Jones R, Roden C, Chalk CJ, Ardlie K, Palescandolo E, Piris A, MacConaill LE, Robert C, Hofbauer GF, McArthur GA, Schadendorf D, et al. RAS mutations are associated with the development of cutaneous squamous cell tumors in patients treated with RAF inhibitors. J Clin Oncol. 2012; 30: 316-321.
-
(2012)
J Clin Oncol.
, vol.30
, pp. 316-321
-
-
Oberholzer, P.A.1
Kee, D.2
Dziunycz, P.3
Sucker, A.4
Kamsukom, N.5
Jones, R.6
Roden, C.7
Chalk, C.J.8
Ardlie, K.9
Palescandolo, E.10
Piris, A.11
Macconaill, L.E.12
Robert, C.13
Hofbauer, G.F.14
McArthur, G.A.15
Schadendorf, D.16
-
50
-
-
80051625929
-
Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling
-
Wagle N, Emery C, Berger MF, Davis MJ, Sawyer A, Pochanard P, Kehoe SM, Johannessen CM, Macconaill LE, Hahn WC, Meyerson M, Garraway LA. Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling. J Clin Oncol. 2011; 29: 3085-3096.
-
(2011)
J Clin Oncol.
, vol.29
, pp. 3085-3096
-
-
Wagle, N.1
Emery, C.2
Berger, M.F.3
Davis, M.J.4
Sawyer, A.5
Pochanard, P.6
Kehoe, S.M.7
Johannessen, C.M.8
Macconaill, L.E.9
Hahn, W.C.10
Meyerson, M.11
Garraway, L.A.12
-
51
-
-
80052420861
-
The beating heart of melanomas: a minor subset of cancer cells sustains tumor growth
-
Schmidt P, Abken H. The beating heart of melanomas: a minor subset of cancer cells sustains tumor growth. Oncotarget. 2011; 2: 313-320.
-
(2011)
Oncotarget
, vol.2
, pp. 313-320
-
-
Schmidt, P.1
Abken, H.2
-
52
-
-
84863216083
-
Regression of metastatic melanoma in a patient by antibody targeting of cancer stem cells
-
Schlaak M, Schmidt P, Bangard C, Kurschat P, Mauch C, Abken H. Regression of metastatic melanoma in a patient by antibody targeting of cancer stem cells. Oncotarget. 2012; 3: 22-30.
-
(2012)
Oncotarget
, vol.3
, pp. 22-30
-
-
Schlaak, M.1
Schmidt, P.2
Bangard, C.3
Kurschat, P.4
Mauch, C.5
Abken, H.6
-
53
-
-
80052424388
-
Characterization of human melanoma cell lines and melanocytes by proteome analysis
-
Caputo E, Maiorana L, Vasta V, Pezzino FM, Sunkara S, Wynne K, Elia G, Marincola FM, McCubrey JA, Libra M, Travali S, Kane M. Characterization of human melanoma cell lines and melanocytes by proteome analysis. Cell Cycle. 2011; 10: 2924-2936.
-
(2011)
Cell Cycle
, vol.10
, pp. 2924-2936
-
-
Caputo, E.1
Maiorana, L.2
Vasta, V.3
Pezzino, F.M.4
Sunkara, S.5
Wynne, K.6
Elia, G.7
Marincola, F.M.8
McCubrey, J.A.9
Libra, M.10
Travali, S.11
Kane, M.12
-
54
-
-
79551544267
-
PRIMA-1Met/ APR-246 induces wild-type p53-dependent suppression of malignant melanoma tumor growth in 3D culture and in vivo
-
Bao W, Chen M, Zhao X, Kumar R, Spinnler C, Thullberg M, Issaeva N, Selivanova G, Stromblad S. PRIMA-1Met/ APR-246 induces wild-type p53-dependent suppression of malignant melanoma tumor growth in 3D culture and in vivo. Cell Cycle. 2011; 10: 301-307.
-
(2011)
Cell Cycle
, vol.10
, pp. 301-307
-
-
Bao, W.1
Chen, M.2
Zhao, X.3
Kumar, R.4
Spinnler, C.5
Thullberg, M.6
Issaeva, N.7
Selivanova, G.8
Stromblad, S.9
-
55
-
-
80052394805
-
Using quantitative proteomic analysis to understand genotype specific intrinsic drugresistance in melanoma
-
Koomen JM, Smalley KS. Using quantitative proteomic analysis to understand genotype specific intrinsic drugresistance in melanoma. Oncotarget. 2011; 2: 329-335.
-
(2011)
Oncotarget
, vol.2
, pp. 329-335
-
-
Koomen, J.M.1
Smalley, K.S.2
-
56
-
-
84055179140
-
Chronic myeloid leukemia stem cells in the era of targeted therapies: resistance, persistence and long-term dormancy
-
Chomel JC, Turhan AG. Chronic myeloid leukemia stem cells in the era of targeted therapies: resistance, persistence and long-term dormancy. Oncotarget. 2011; 2: 713-727.
-
(2011)
Oncotarget
, vol.2
, pp. 713-727
-
-
Chomel, J.C.1
Turhan, A.G.2
-
57
-
-
77956407620
-
Hedgehog pathway activation in chronic myeloid leukemia
-
Jagani Z, Dorsch M, Warmuth M. Hedgehog pathway activation in chronic myeloid leukemia. Cell Cycle. 2010; 9: 3449-3456.
-
(2010)
Cell Cycle
, vol.9
, pp. 3449-3456
-
-
Jagani, Z.1
Dorsch, M.2
Warmuth, M.3
-
58
-
-
79551536292
-
Impact of BCR-ABL mutations on patients with chronic myeloid leukemia
-
Hochhaus A, La Rosee P, Muller MC, Ernst T, Cross NC. Impact of BCR-ABL mutations on patients with chronic myeloid leukemia. Cell Cycle. 2011; 10: 250-260.
-
(2011)
Cell Cycle
, vol.10
, pp. 250-260
-
-
Hochhaus, A.1
Rosee, P.L.2
Muller, M.C.3
Ernst, T.4
Cross, N.C.5
-
59
-
-
77955602211
-
Gatekeeper mutations mediate resistance to BRAF-targeted therapies
-
Whittaker S, Kirk R, Hayward R, Zambon A, Viros A, Cantarino N, Affolter A, Nourry A, Niculescu-Duvaz D, Springer C, Marais R. Gatekeeper mutations mediate resistance to BRAF-targeted therapies. Sci Transl Med. 2010; 2: 35ra41.
-
(2010)
Sci Transl Med.
, vol.2
, pp. 35-41
-
-
Whittaker, S.1
Kirk, R.2
Hayward, R.3
Zambon, A.4
Viros, A.5
Cantarino, N.6
Affolter, A.7
Nourry, A.8
Niculescu-Duvaz, D.9
Springer, C.10
Marais, R.11
-
60
-
-
78650303507
-
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
-
Nazarian R, Shi H, Wang Q, Kong X, Koya RC, Lee H, Chen Z, Lee MK, Attar N, Sazegar H, Chodon T, Nelson SF, McArthur G, Sosman JA, Ribas A, Lo RS. Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation. Nature. 2010; 468: 973-977.
-
(2010)
Nature
, vol.468
, pp. 973-977
-
-
Nazarian, R.1
Shi, H.2
Wang, Q.3
Kong, X.4
Koya, R.C.5
Lee, H.6
Chen, Z.7
Lee, M.K.8
Attar, N.9
Sazegar, H.10
Chodon, T.11
Nelson, S.F.12
McArthur, G.13
Sosman, J.A.14
Ribas, A.15
Lo, R.S.16
-
61
-
-
83455254767
-
RAF inhibitor resistance is mediated by dimerization of aberrantly spliced BRAF(V600E)
-
Poulikakos PI, Persaud Y, Janakiraman M, Kong X, Ng C, Moriceau G, Shi H, Atefi M, Titz B, Gabay MT, Salton M, Dahlman KB, Tadi M, Wargo JA, Flaherty KT, Kelley MC, et al. RAF inhibitor resistance is mediated by dimerization of aberrantly spliced BRAF(V600E). Nature. 2011; 480: 387-390.
-
(2011)
Nature
, vol.480
, pp. 387-390
-
-
Poulikakos, P.I.1
Persaud, Y.2
Janakiraman, M.3
Kong, X.4
Ng, C.5
Moriceau, G.6
Shi, H.7
Atefi, M.8
Titz, B.9
Gabay, M.T.10
Salton, M.11
Dahlman, K.B.12
Tadi, M.13
Wargo, J.A.14
Flaherty, K.T.15
Kelley, M.C.16
-
62
-
-
84859471412
-
Targeting mutant BRAF in melanoma: current status and future development of combination therapy strategies
-
Kudchadkar R, Paraiso KH, Smalley KS. Targeting mutant BRAF in melanoma: current status and future development of combination therapy strategies. Cancer J. 2012; 18: 124-131.
-
(2012)
Cancer J.
, vol.18
, pp. 124-131
-
-
Kudchadkar, R.1
Paraiso, K.H.2
Smalley, K.S.3
-
64
-
-
54049158957
-
Increased cyclin D1 expression can mediate BRAF inhibitor resistance in BRAF V600E-mutated melanomas
-
Smalley KS, Lioni M, Dalla Palma M, Xiao M, Desai B, Egyhazi S, Hansson J, Wu H, King AJ, Van Belle P, Elder DE, Flaherty KT, Herlyn M, Nathanson KL. Increased cyclin D1 expression can mediate BRAF inhibitor resistance in BRAF V600E-mutated melanomas. Mol Cancer Ther. 2008; 7: 2876-2883.
-
(2008)
Mol Cancer Ther.
, vol.7
, pp. 2876-2883
-
-
Smalley, K.S.1
Lioni, M.2
Dalla Palma, M.3
Xiao, M.4
Desai, B.5
Egyhazi, S.6
Hansson, J.7
Wu, H.8
King, A.J.9
Van Belle, P.10
Elder, D.E.11
Flaherty, K.T.12
Herlyn, M.13
Nathanson, K.L.14
-
65
-
-
78649436372
-
BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation
-
Corcoran RB, Dias-Santagata D, Bergethon K, Iafrate AJ, Settleman J, Engelman JA, BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation. Sci Signal. 2010; 3: ra84.
-
(2010)
Sci Signal
, vol.3
-
-
Corcoran, R.B.1
Dias-Santagata, D.2
Bergethon, K.3
Iafrate, A.J.4
Settleman, J.5
Engelman, J.A.6
-
66
-
-
84859183431
-
-
Shi H, Moriceau G, Kong X, Lee MK, Lee H, Koya RC, Ng C, Chodon T, Scolyer RA, Dahlman KB, Sosman JA, Kefford RF, Long GV, Nelson SF, Ribas A, Lo RS. Melanoma whole-exome sequencing identifies (V600E) B-RAF amplification-mediated acquired B-RAF inhibitor resistance Nat Commun. 2012; 3: 724.
-
(2012)
Melanoma whole-exome sequencing identifies (V600E) B-RAF amplification-mediated acquired B-RAF inhibitor resistance Nat Commun
, vol.3
, pp. 724
-
-
Shi, H.1
Moriceau, G.2
Kong, X.3
Lee, M.K.4
Lee, H.5
Koya, R.C.6
Ng, C.7
Chodon, T.8
Scolyer, R.A.9
Dahlman, K.B.10
Sosman, J.A.11
Kefford, R.F.12
Long, G.V.13
Nelson, S.F.14
Ribas, A.15
Lo, R.S.16
-
67
-
-
78650309875
-
COT drives resistance to RAF inhibition through MAP kinase pathway reactivation
-
Johannessen CM, Boehm JS, Kim SY, Thomas SR, Wardwell L, Johnson LA, Emery CM, Stransky N, Cogdill AP, Barretina J, Caponigro G, Hieronymus H, Murray RR, Salehi-Ashtiani K, Hill DE, Vidal M, et al. COT drives resistance to RAF inhibition through MAP kinase pathway reactivation. Nature. 2010; 468: 968-972.
-
(2010)
Nature
, vol.468
, pp. 968-972
-
-
Johannessen, C.M.1
Boehm, J.S.2
Kim, S.Y.3
Thomas, S.R.4
Wardwell, L.5
Johnson, L.A.6
Emery, C.M.7
Stransky, N.8
Cogdill, A.P.9
Barretina, J.10
Caponigro, G.11
Hieronymus, H.12
Murray, R.R.13
Salehi-Ashtiani, K.14
Hill, D.E.15
Vidal, M.16
-
68
-
-
61349189102
-
-
Cusack K, Allen H, Bischoff A, Clabbers A, Dixon R, Fix-Stenzel S, Friedman M, Gaumont Y, George D, Gordon T, Grongsaard P, Janssen B, Jia Y, Moskey M, Quinn C, Salmeron A, et al. Identification of a selective thieno[2,3-c] pyridine inhibitor of COT kinase and TNF-alpha production Bioorg Med Chem Lett. 2009; 19: 1722-1725.
-
(2009)
Identification of a selective thieno[2,3-c] pyridine inhibitor of COT kinase and TNF-alpha production Bioorg Med Chem Lett
, vol.19
, pp. 1722-1725
-
-
Cusack, K.1
Allen, H.2
Bischoff, A.3
Clabbers, A.4
Dixon, R.5
Fix-Stenzel, S.6
Friedman, M.7
Gaumont, Y.8
George, D.9
Gordon, T.10
Grongsaard, P.11
Janssen, B.12
Jia, Y.13
Moskey, M.14
Quinn, C.15
Salmeron, A.16
-
69
-
-
78650008177
-
Acquired resistance to BRAF inhibitors mediated by a RAF kinase switch in melanoma can be overcome by cotargeting MEK and IGF-1R/PI3K
-
Villanueva J, Vultur A, Lee JT, Somasundaram R, Fukunaga-Kalabis M, Cipolla AK, Wubbenhorst B, Xu X, Gimotty PA, Kee D, Santiago-Walker AE, Letrero R, D'Andrea K, Pushparajan A, Hayden JE, Brown KD, et al. Acquired resistance to BRAF inhibitors mediated by a RAF kinase switch in melanoma can be overcome by cotargeting MEK and IGF-1R/PI3K. Cancer Cell. 2010; 18: 683-695.
-
(2010)
Cancer Cell
, vol.18
, pp. 683-695
-
-
Villanueva, J.1
Vultur, A.2
Lee, J.T.3
Somasundaram, R.4
Fukunaga-Kalabis, M.5
Cipolla, A.K.6
Wubbenhorst, B.7
Xu, X.8
Gimotty, P.A.9
Kee, D.10
Santiago-Walker, A.E.11
Letrero, R.12
D'Andrea, K.13
Pushparajan, A.14
Hayden, J.E.15
Brown, K.D.16
-
70
-
-
79953325104
-
PTEN loss confers BRAF inhibitor resistance to melanoma cells through the suppression of BIM expression
-
Paraiso KH, Xiang Y, Rebecca VW, Abel EV, Chen YA, Munko AC, Wood E, Fedorenko IV, Sondak VK, Anderson AR, Ribas A, Palma MD, Nathanson KL, Koomen JM, Messina JL, Smalley KS. PTEN loss confers BRAF inhibitor resistance to melanoma cells through the suppression of BIM expression. Cancer Res. 2011; 71: 2750-2760.
-
(2011)
Cancer Res.
, vol.71
, pp. 2750-2760
-
-
Paraiso, K.H.1
Xiang, Y.2
Rebecca, V.W.3
Abel, E.V.4
Chen, Y.A.5
Munko, A.C.6
Wood, E.7
Fedorenko, I.V.8
Sondak, V.K.9
Anderson, A.R.10
Ribas, A.11
Palma, M.D.12
Nathanson, K.L.13
Koomen, J.M.14
Messina, J.L.15
Smalley, K.S.16
-
71
-
-
79958785634
-
Protein kinase D3 sensitizes RAF inhibitor RAF265 in melanoma cells by preventing reactivation of MAPK signaling
-
Chen J, Shen Q, Labow M, Gaither LA. Protein kinase D3 sensitizes RAF inhibitor RAF265 in melanoma cells by preventing reactivation of MAPK signaling. Cancer Res. 2011; 71: 4280-4291.
-
(2011)
Cancer Res.
, vol.71
, pp. 4280-4291
-
-
Chen, J.1
Shen, Q.2
Labow, M.3
Gaither, L.A.4
-
72
-
-
57749100261
-
Potent and selective disruption of protein kinase D functionality by a benzoxoloazepinolone
-
Sharlow ER, Giridhar KV, LaValle CR, Chen J, Leimgruber S, Barrett R, Bravo-Altamirano K, Wipf P, Lazo JS, Wang QJ. Potent and selective disruption of protein kinase D functionality by a benzoxoloazepinolone. J Biol Chem. 2008; 283: 33516-3326.
-
(2008)
J Biol Chem.
, vol.283
, pp. 33516-33326
-
-
Sharlow, E.R.1
Giridhar, K.V.2
LaValle, C.R.3
Chen, J.4
Leimgruber, S.5
Barrett, R.6
Bravo-Altamirano, K.7
Wipf, P.8
Lazo, J.S.9
Wang, Q.J.10
-
73
-
-
84864285794
-
Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion
-
Straussman R, Morikawa T, Shee K, Barzily-Rokni M, Qian ZR, Du J, Davis A, Mongare MM, Gould J, Frederick DT, Cooper ZA, Chapman PB, Solit DB, Ribas A, Lo RS, Flaherty KT, et al. Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion. Nature. 2012; 487: 500-504.
-
(2012)
Nature
, vol.487
, pp. 500-504
-
-
Straussman, R.1
Morikawa, T.2
Shee, K.3
Barzily-Rokni, M.4
Qian, Z.R.5
Du, J.6
Davis, A.7
Mongare, M.M.8
Gould, J.9
Frederick, D.T.10
Cooper, Z.A.11
Chapman, P.B.12
Solit, D.B.13
Ribas, A.14
Lo, R.S.15
Flaherty, K.T.16
-
74
-
-
84864286442
-
Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors
-
Wilson TR, Fridlyand J, Yan Y, Penuel E, Burton L, Chan E, Peng J, Lin E, Wang Y, Sosman J, Ribas A, Li J, Moffat J, Sutherlin DP, Koeppen H, Merchant M, et al. Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors. Nature. 2012; 487: 505-509.
-
(2012)
Nature
, vol.487
, pp. 505-509
-
-
Wilson, T.R.1
Fridlyand, J.2
Yan, Y.3
Penuel, E.4
Burton, L.5
Chan, E.6
Peng, J.7
Lin, E.8
Wang, Y.9
Sosman, J.10
Ribas, A.11
Li, J.12
Moffat, J.13
Sutherlin, D.P.14
Koeppen, H.15
Merchant, M.16
-
75
-
-
50649090571
-
Advances in the development of cancer therapeutics directed against the Ras-mitogen-activated protein kinase pathway
-
Sebolt-Leopold JS. Advances in the development of cancer therapeutics directed against the Ras-mitogen-activated protein kinase pathway. Clin Cancer Res. 2008; 14: 3651-3656.
-
(2008)
Clin Cancer Res.
, vol.14
, pp. 3651-3656
-
-
Sebolt-Leopold, J.S.1
-
76
-
-
77951016969
-
A phase II study of PD-0325901, an oral MEK inhibitor, in previously treated patients with advanced non-small cell lung cancer
-
Haura EB, Ricart AD, Larson TG, Stella PJ, Bazhenova L, Miller VA, Cohen RB, Eisenberg PD, Selaru P, Wilner KD, Gadgeel SM. A phase II study of PD-0325901, an oral MEK inhibitor, in previously treated patients with advanced non-small cell lung cancer. Clin Cancer Res. 2010; 16: 2450-2457.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 2450-2457
-
-
Haura, E.B.1
Ricart, A.D.2
Larson, T.G.3
Stella, P.J.4
Bazhenova, L.5
Miller, V.A.6
Cohen, R.B.7
Eisenberg, P.D.8
Selaru, P.9
Wilner, K.D.10
Gadgeel, S.M.11
-
77
-
-
77949766280
-
Phase I pharmacokineticand pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers
-
LoRusso PM, Krishnamurthi SS, Rinehart JJ, Nabell LM, Malburg L, Chapman PB, DePrimo SE, Bentivegna S, Wilner KD, Tan W, Ricart AD. Phase I pharmacokineticand pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers. Clin Cancer Res. 2010; 16: 1924-1937.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 1924-1937
-
-
LoRusso, P.M.1
Krishnamurthi, S.S.2
Rinehart, J.J.3
Nabell, L.M.4
Malburg, L.5
Chapman, P.B.6
DePrimo, S.E.7
Bentivegna, S.8
Wilner, K.D.9
Tan, W.10
Ricart, A.D.11
-
78
-
-
84861771818
-
Bridging the gap between preclinical and clinical studies using pharmacokinetic-pharmacodynamic (PK-PD) modeling: An analysis of GDC-0973, a MEK Inhibitor
-
Wong H, Vernillet L, Peterson A, Ware JA, Lee L, Martini JF, Yu P, Li C, Del Rosario G, Choo EF, Hoeflich KP, Shi Y, Aftab BT, Aoyama R, Lam ST, Belvin M, et al. Bridging the gap between preclinical and clinical studies using pharmacokinetic-pharmacodynamic (PK-PD) modeling: An analysis of GDC-0973, a MEK Inhibitor. Clin Cancer Res. 2012; 18: 3090-3099.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 3090-3099
-
-
Wong, H.1
Vernillet, L.2
Peterson, A.3
Ware, J.A.4
Lee, L.5
Martini, J.F.6
Yu, P.7
Li, C.8
Del Rosario, G.9
Choo, E.F.10
Hoeflich, K.P.11
Shi, Y.12
Aftab, B.T.13
Aoyama, R.14
Lam, S.T.15
Belvin, M.16
-
79
-
-
34548097240
-
AZD6244 (ARRY 142886) a potent inhibitor of mitogen-activated protein kinase/extracellular signal-related kinase kinase 1 /2 kinases: mechanism of action in vivo, pharmacokinetic/ pharmacodynamic relationship and potential for combination in preclinical models
-
Davies BD, Logie A, McKay JS, Martin P, Steele S, Jenkins R, Cockerill M, Cartlidge S, Smith PD. AZD6244 (ARRY 142886) a potent inhibitor of mitogen-activated protein kinase/extracellular signal-related kinase kinase 1 /2 kinases: mechanism of action in vivo, pharmacokinetic/ pharmacodynamic relationship and potential for combination in preclinical models. Mol Cancer Ther. 2007; 6: 2209-2219.
-
(2007)
Mol Cancer Ther.
, vol.6
, pp. 2209-2219
-
-
Davies, B.D.1
Logie, A.2
McKay, J.S.3
Martin, P.4
Steele, S.5
Jenkins, R.6
Cockerill, M.7
Cartlidge, S.8
Smith, P.D.9
-
81
-
-
1442335098
-
Multiple anticancer effects of blocking MEK-ERK signaling in hepatocellular carcinoma
-
Wiesenauer CA, Yip-Schneider MT, Wang Y, Schmidt CM. Multiple anticancer effects of blocking MEK-ERK signaling in hepatocellular carcinoma. J Am Coll Surg. 2004; 198: 410-421.
-
(2004)
J Am Coll Surg.
, vol.198
, pp. 410-421
-
-
Wiesenauer, C.A.1
Yip-Schneider, M.T.2
Wang, Y.3
Schmidt, C.M.4
-
82
-
-
38349071703
-
Targeting MEK is effective chemoprevention of hepatocellular carcinoma in TGFalpha-transgenic mice
-
Wentz SC, Wu H, Yip-Schneider MT, Hennig M, Klein PJ, Sebolt-Leopold, Schmidt CM.. Targeting MEK is effective chemoprevention of hepatocellular carcinoma in TGFalpha-transgenic mice. J Gastrointest Surg. 2008; 12: 30-37.
-
(2008)
J Gastrointest Surg.
, vol.12
, pp. 30-37
-
-
Wentz, S.C.1
Wu, H.2
Yip-Schneider, M.T.3
Hennig, M.4
Klein, P.J.5
Sebolt-Leopold, S.C.M.6
-
83
-
-
70149119899
-
RDEA119/BAY 869766: a potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer
-
Iverson C, Larson G, Lai C, Yeh LT, Dadson C, Weingarten P, Appleby T, Vo T, Maderna A, Vernier JM, Hamatake R, Miner JN, Quart B. RDEA119/BAY 869766: a potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer. Cancer Res. 2009; 69: 6839-6847.
-
(2009)
Cancer Res.
, vol.69
, pp. 6839-6847
-
-
Iverson, C.1
Larson, G.2
Lai, C.3
Yeh, L.T.4
Dadson, C.5
Weingarten, P.6
Appleby, T.7
Vo, T.8
Maderna, A.9
Vernier, J.M.10
Hamatake, R.11
Miner, J.N.12
Quart, B.13
-
84
-
-
78249243102
-
BRAF mutation-selective inhibition of thyroid cancer cells by the novel MEK inhibitor RDEA119 and genetic-potentiated synergism with the mTOR inhibitor temsirolimus
-
Liu D, Xing J, Trink B, Xing M. BRAF mutation-selective inhibition of thyroid cancer cells by the novel MEK inhibitor RDEA119 and genetic-potentiated synergism with the mTOR inhibitor temsirolimus. Int J Cancer. 2010; 127: 2965-2973.
-
(2010)
Int J Cancer.
, vol.127
, pp. 2965-2973
-
-
Liu, D.1
Xing, J.2
Trink, B.3
Xing, M.4
-
85
-
-
77957164869
-
Antitumour activity of a potent MEK inhibitor RDEA119/BAY 869766 combined with rapamycin in human orthotopic primary pancreatic cancer xenografts
-
Chang Q, Chapman MS, Miner JN, Hedley DW. Antitumour activity of a potent MEK inhibitor RDEA119/BAY 869766 combined with rapamycin in human orthotopic primary pancreatic cancer xenografts. BMC Cancer. 2010; 10: 515.
-
(2010)
BMC Cancer
, vol.10
, pp. 515
-
-
Chang, Q.1
Chapman, M.S.2
Miner, J.N.3
Hedley, D.W.4
-
86
-
-
84862732834
-
Combinations of BRAF, MEK, and PI3K/mTOR inhibitors overcome acquired resistance to the BRAF inhibitor GSK2118436 dabrafenib, mediated by NRAS or MEK mutations
-
Greger J, Eastman S, Zhang V, Bleam MR, Hughes A, Smitheman KN, Dickerson S, Laquerre S, Liu L, Gilmer TM. Combinations of BRAF, MEK, and PI3K/mTOR inhibitors overcome acquired resistance to the BRAF inhibitor GSK2118436 dabrafenib, mediated by NRAS or MEK mutations. Mol Cancer Ther. 2012; 11: 909-920.
-
(2012)
Mol Cancer Ther.
, vol.11
, pp. 909-920
-
-
Greger, J.1
Eastman, S.2
Zhang, V.3
Bleam, M.R.4
Hughes, A.5
Smitheman, K.N.6
Dickerson, S.7
Laquerre, S.8
Liu, L.9
Gilmer, T.M.10
-
87
-
-
84855415767
-
Intermittent administration of MEK inhibitor GDC-0973 plus PI3K inhibitor GDC-0941 triggers robust apoptosis and tumor growth inhibition
-
Hoeflich KP, Merchant M, Orr C, Chan J, Den Otter D, Berry L, Kasman I, Koeppen H, Rice K, Yang NY, Engst S, Johnston S, Friedman LS, Belvin M. Intermittent administration of MEK inhibitor GDC-0973 plus PI3K inhibitor GDC-0941 triggers robust apoptosis and tumor growth inhibition. Cancer Res. 2012; 72: 210-219.
-
(2012)
Cancer Res.
, vol.72
, pp. 210-219
-
-
Hoeflich, K.P.1
Merchant, M.2
Orr, C.3
Chan, J.4
Den Otter, D.5
Berry, L.6
Kasman, I.7
Koeppen, H.8
Rice, K.9
Yang, N.Y.10
Engst, S.11
Johnston, S.12
Friedman, L.S.13
Belvin, M.14
-
88
-
-
78751480476
-
MEK1/2 inhibitors AS703026 and AZD6244 may be potential therapies for KRAS mutated colorectal cancer that is resistant to EGFR monoclonal antibody therapy
-
Yoon J, Koo KH, Choi KY. MEK1/2 inhibitors AS703026 and AZD6244 may be potential therapies for KRAS mutated colorectal cancer that is resistant to EGFR monoclonal antibody therapy. Cancer Res. 2011; 71: 445-453.
-
(2011)
Cancer Res.
, vol.71
, pp. 445-453
-
-
Yoon, J.1
Koo, K.H.2
Choi, K.Y.3
-
89
-
-
77951678924
-
Blockade of the MEK/ERK signalling cascade by AS703026, a novel selective MEK1/2 inhibitor, induces pleiotropic anti-myeloma activity in vitro and in vivo
-
Kim K, Kong SY, Fulciniti M, Li X, Song W, Nahar S, Burger P, Rumizen MJ, Podar K, Chauhan D, Hideshima T, Munshi NC, Richardson P, Clark A, Ogden J, Goutopoulos A, et al. Blockade of the MEK/ERK signalling cascade by AS703026, a novel selective MEK1/2 inhibitor, induces pleiotropic anti-myeloma activity in vitro and in vivo. Br J Haematol. 2010; 149: 537-549.
-
(2010)
Br J Haematol.
, vol.149
, pp. 537-549
-
-
Kim, K.1
Kong, S.Y.2
Fulciniti, M.3
Li, X.4
Song, W.5
Nahar, S.6
Burger, P.7
Rumizen, M.J.8
Podar, K.9
Chauhan, D.10
Hideshima, T.11
Munshi, N.C.12
Richardson, P.13
Clark, A.14
Ogden, J.15
Goutopoulos, A.16
-
90
-
-
73149086864
-
The safety, tolerability, pharmacokinetics, and pharmacodynamics of single oral doses of CH4987655 in healthy volunteers: target suppression using a biomarker
-
Lee L, Niu H, Rueger R, Igawa Y, Deutsch J, Ishii N, Mu S, Sakamoto Y, Busse-Reid R, Gimmi C, Goelzer P, De Schepper S, Yoshimura Y, Barrett J, Ishikawa Y, Weissgerber G, et al. The safety, tolerability, pharmacokinetics, and pharmacodynamics of single oral doses of CH4987655 in healthy volunteers: target suppression using a biomarker. Clin Cancer Res. 2009; 15: 7368-7374.
-
(2009)
Clin Cancer Res.
, vol.15
, pp. 7368-7374
-
-
Lee, L.1
Niu, H.2
Rueger, R.3
Igawa, Y.4
Deutsch, J.5
Ishii, N.6
Mu, S.7
Sakamoto, Y.8
Busse-Reid, R.9
Gimmi, C.10
Goelzer, P.11
De Schepper, S.12
Yoshimura, Y.13
Barrett, J.14
Ishikawa, Y.15
Weissgerber, G.16
-
91
-
-
79951722555
-
Discovery of TAK-733, a potent and selective MEK allosteric site inhibitor for the treatment of cancer
-
Dong Q, Dougan DR, Gong X, Halkowycz P, Jin B, Kanouni T, O'Connell SM, Scorah N, Shi L, Wallace MB, Zhou F. Discovery of TAK-733, a potent and selective MEK allosteric site inhibitor for the treatment of cancer. Bioorg Med Chem Lett. 2011; 21: 1315-1319.
-
(2011)
Bioorg Med Chem Lett.
, vol.21
, pp. 1315-1319
-
-
Dong, Q.1
Dougan, D.R.2
Gong, X.3
Halkowycz, P.4
Jin, B.5
Kanouni, T.6
O'Connell, S.M.7
Scorah, N.8
Shi, L.9
Wallace, M.B.10
Zhou, F.11
-
92
-
-
79959954934
-
The MEK inhibitor SL327 blocks acquisition but not expression of lithiuminduced conditioned place aversion: a behavioral and immunohistochemical study
-
Longoni R, Spina L, Vinci S, Acquas E. The MEK inhibitor SL327 blocks acquisition but not expression of lithiuminduced conditioned place aversion: a behavioral and immunohistochemical study. Psychopharmacology (Berl). 2011; 216: 63-73.
-
(2011)
Psychopharmacology (Berl).
, vol.216
, pp. 63-73
-
-
Longoni, R.1
Spina, L.2
Vinci, S.3
Acquas, E.4
-
93
-
-
79959283388
-
Multi-institutional phase II study of selumetinib in patients with metastatic biliary cancers
-
Tanios Bekaii-Saab T, Phelps MA, Li X, Saji M, Goff L, Kauh JSW, O'Neil BH, Balsom S, Balint S, Liersemann R, Vasko VV, Bloomston M, Marsh W, Doyle LA, Ellison G, Grever M, et al. Multi-institutional phase II study of selumetinib in patients with metastatic biliary cancers. JCO. 2011; 29: 2357-2363.
-
(2011)
JCO.
, vol.29
, pp. 2357-2363
-
-
Tanios Bekaii-Saab, T.1
Phelps, M.A.2
Li, X.3
Saji, M.4
Goff, L.5
Kauh, J.S.W.6
O'Neil, B.H.7
Balsom, S.8
Balint, S.9
Liersemann, R.10
Vasko, V.V.11
Bloomston, M.12
Marsh, W.13
Doyle, L.A.14
Ellison, G.15
Grever, M.16
-
94
-
-
77953552589
-
Novel combination of celecoxib and proteasome inhibitor MG132 provides synergistic antiproliferative and proapoptotic effects in human liver tumor cells
-
Cusimano A, Azzolina A, Iovanna JL, Bachvarov D, McCubrey JA, D'Alessandro N, Montalto G, Cervello M. Novel combination of celecoxib and proteasome inhibitor MG132 provides synergistic antiproliferative and proapoptotic effects in human liver tumor cells. Cell Cycle. 2010; 9: 1399-1410.
-
(2010)
Cell Cycle
, vol.9
, pp. 1399-1410
-
-
Cusimano, A.1
Azzolina, A.2
Iovanna, J.L.3
Bachvarov, D.4
Mccubrey, J.A.5
D'Alessandro, N.6
Montalto, G.7
Cervello, M.8
-
95
-
-
84861460801
-
The novel NF-kappaB inhibitor DHMEQ synergizes with celecoxib to exert antitumor effects on human liver cancer cells by a ROS-dependent mechanism
-
Lampiasi N, Azzolina A, Umezawa K, Montalto G, McCubrey JA, Cervello M. The novel NF-kappaB inhibitor DHMEQ synergizes with celecoxib to exert antitumor effects on human liver cancer cells by a ROS-dependent mechanism. Cancer Lett. 2012; 322: 35-44.
-
(2012)
Cancer Lett.
, vol.322
, pp. 35-44
-
-
Lampiasi, N.1
Azzolina, A.2
Umezawa, K.3
Montalto, G.4
McCubrey, J.A.5
Cervello, M.6
-
96
-
-
79954775922
-
Targeted cellular metabolism for cancer chemotherapy with recombinant argininedegrading enzymes
-
Kuo MT, Savaraj N, Feun LG. Targeted cellular metabolism for cancer chemotherapy with recombinant argininedegrading enzymes. Oncotarget. 2010; 1: 246-251.
-
(2010)
Oncotarget
, vol.1
, pp. 246-251
-
-
Kuo, M.T.1
Savaraj, N.2
Feun, L.G.3
-
97
-
-
79957480596
-
Mouse models of hepatocarcinogenesis: what can we learn for the prevention of human hepatocellular carcinoma?
-
Vucur M, Roderburg C, Bettermann K, Tacke F, Heikenwalder M, Trautwein C, Luedde T. Mouse models of hepatocarcinogenesis: what can we learn for the prevention of human hepatocellular carcinoma?. Oncotarget. 2010; 1:373-378.
-
(2010)
Oncotarget
, vol.1
, pp. 73-378
-
-
Vucur, M.1
Roderburg, C.2
Bettermann, K.3
Tacke, F.4
Heikenwalder, M.5
Trautwein, C.6
Luedde, T.7
-
98
-
-
77958492734
-
Glutaminolysis: supplying carbon or nitrogen or both for cancer cells?
-
Dang CV. Glutaminolysis: supplying carbon or nitrogen or both for cancer cells? Cell Cycle. 2010; 9: 3884-3886.
-
(2010)
Cell Cycle
, vol.9
, pp. 3884-3886
-
-
Dang, C.V.1
-
99
-
-
77956409919
-
IL-6, a risk factor for hepatocellular carcinoma: FLLL32 inhibits IL-6-induced STAT3 phosphorylation in human hepatocellular cancer cells
-
Liu Y, Fuchs J, Li C, Lin J. IL-6, a risk factor for hepatocellular carcinoma: FLLL32 inhibits IL-6-induced STAT3 phosphorylation in human hepatocellular cancer cells. Cell Cycle. 2010;9: 3423-3427.
-
(2010)
Cell Cycle
, vol.9
, pp. 3423-3427
-
-
Liu, Y.1
Fuchs, J.2
Li, C.3
Lin, J.4
-
100
-
-
84865749357
-
First-in-Human, Phase I Dose-Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of RO5126766, a First-in-Class Dual MEK/RAF Inhibitor in Patients with Solid Tumors
-
Martinez-Garcia M, Banerji U, Albanell J, Bahleda R, Dolly S, Kraeber-Bodéré F, Rojo F, Routier E, Guarin E, Xu ZX, Rueger R, Tessier JJ, Shochat E, Blotner S, Naegelen VM, Soria JC. First-in-Human, Phase I Dose-Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of RO5126766, a First-in-Class Dual MEK/RAF Inhibitor in Patients with Solid Tumors. Clin Cancer Res. 2012; 18: 4806-4819.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 4806-4819
-
-
Martinez-Garcia, M.1
Banerji, U.2
Albanell, J.3
Bahleda, R.4
Dolly, S.5
Kraeber-Bodéré, F.6
Rojo, F.7
Routier, E.8
Guarin, E.9
Xu, Z.X.10
Rueger, R.11
Tessier, J.J.12
Shochat, E.13
Blotner, S.14
Naegelen, V.M.15
Soria, J.C.16
-
101
-
-
55949097252
-
Genetic predictors of MEK dependence in non-small cell lung cancer
-
Pratilas CA, Hanrahan AJ, Halilovic E, Persaud Y, Soh J, Chitale D, Shigematsu H, Yamamoto H, Sawai A, Janakiraman M, Taylor BS, Pao W, Toyooka S, Ladanyi M, Gazdar A, Rosen N, et al. Genetic predictors of MEK dependence in non-small cell lung cancer. Cancer Res. 2008; 68: 9375-9383.
-
(2008)
Cancer Res.
, vol.68
, pp. 9375-9383
-
-
Pratilas, C.A.1
Hanrahan, A.J.2
Halilovic, E.3
Persaud, Y.4
Soh, J.5
Chitale, D.6
Shigematsu, H.7
Yamamoto, H.8
Sawai, A.9
Janakiraman, M.10
Taylor, B.S.11
Pao, W.12
Toyooka, S.13
Ladanyi, M.14
Gazdar, A.15
Rosen, N.16
-
102
-
-
66249116702
-
PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers
-
Wee S, Jagani Z, Xiang KX, Loo A, Dorsch M, Yao YM, Seller WR, Lengauer C, Stegmeier F. PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers. Cancer Res. 2099; 69: 4286-4293.
-
Cancer Res.
, vol.69
, pp. 4286-4293
-
-
Wee, S.1
Jagani, Z.2
Xiang, K.X.3
Loo, A.4
Dorsch, M.5
Yao, Y.M.6
Seller, W.R.7
Lengauer, C.8
Stegmeier, F.9
-
103
-
-
68049085887
-
In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase in basal-like breast cancer models
-
Hoeflich KP, O'Brien C, Boyd Z, Cavet G, Guerrero S, Jung K, Januario T, Savage H, Punnoose E, Truong T, Zhou W, Berry L, Murray L, Amler L, Belvin M, Friedman LS, et al. In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase in basal-like breast cancer models. Clin Cancer Res. 2009; 15: 4649-4664.
-
(2009)
Clin Cancer Res.
, vol.15
, pp. 4649-4664
-
-
Hoeflich, K.P.1
O'Brien, C.2
Boyd, Z.3
Cavet, G.4
Guerrero, S.5
Jung, K.6
Januario, T.7
Savage, H.8
Punnoose, E.9
Truong, T.10
Zhou, W.11
Berry, L.12
Murray, L.13
Amler, L.14
Belvin, M.15
Friedman, L.S.16
-
104
-
-
77953500567
-
Differences underlying EGFR and HER2 oncogene addiction
-
Faber AC, Wong KK, Engelman JA. Differences underlying EGFR and HER2 oncogene addiction. Cell Cycle. 2010; 9: 851-852.
-
(2010)
Cell Cycle.
, vol.9
, pp. 851-852
-
-
Faber, A.C.1
Wong, K.K.2
Engelman, J.A.3
-
105
-
-
77953589767
-
A growing family: adding mutated Erbb4 as a novel cancer target
-
Rudloff U, Samuels Y. A growing family: adding mutated Erbb4 as a novel cancer target. Cell Cycle. 2010; 9: 1487-1503.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1487-1503
-
-
Rudloff, U.1
Samuels, Y.2
-
106
-
-
79952344515
-
Stat1 is a suppressor of ErbB2/ Neu-mediated cellular transformation and mouse mammary gland tumor formation
-
Raven JF, Williams V, Wang S, Tremblay ML, Muller WJ, Durbin JE, Koromilas AE. Stat1 is a suppressor of ErbB2/ Neu-mediated cellular transformation and mouse mammary gland tumor formation. Cell Cycle. 2011; 10: 794-804.
-
(2011)
Cell Cycle.
, vol.10
, pp. 794-804
-
-
Raven, J.F.1
Williams, V.2
Wang, S.3
Tremblay, M.L.4
Muller, W.J.5
Durbin, J.E.6
Koromilas, A.E.7
-
107
-
-
77953481991
-
The Met receptor tyrosine kinase and basal breast cancer
-
Ponzo MG. Park M. The Met receptor tyrosine kinase and basal breast cancer. Cell Cycle. 2010; 9: 1043-1050.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1043-1050
-
-
Ponzo, M.G.1
Park, M.2
-
108
-
-
80052398902
-
Cell Cycle. Involvement of Akt and mTOR in chemotherapeuticand hormonal-based drug resistance and response to radiation in breast cancer cells
-
Steelman LS, Navolanic P, Chappell WH, Abrams SL, Wong EW, Martelli AM, Cocco L, Stivala F, Libra M, Nicoletti F, Drobot LB, Franklin RA, McCubrey JA. Cell Cycle. Involvement of Akt and mTOR in chemotherapeuticand hormonal-based drug resistance and response to radiation in breast cancer cells. Cell Cycle. 2011; 10: 3003-3015.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3003-3015
-
-
Steelman, L.S.1
Navolanic, P.2
Chappell, W.H.3
Abrams, S.L.4
Wong, E.W.5
Martelli, A.M.6
Cocco, L.7
Stivala, F.8
Libra, M.9
Nicoletti, F.10
Drobot, L.B.11
Franklin, R.A.12
Mccubrey, J.A.13
-
109
-
-
79956049096
-
RB1 and p53 at the crossroad of EMT and triple-negative breast cancer
-
Jiang Z, Jones R, Liu JC, Deng T, Robinson T, Chung PE, Wang S, Herschkowitz JI, Egan SE, Perou CM, Zacksenhaus E. RB1 and p53 at the crossroad of EMT and triple-negative breast cancer. Cell Cycle. 2011; 10: 1563-1570.
-
(2011)
Cell Cycle
, vol.10
, pp. 1563-1570
-
-
Jiang, Z.1
Jones, R.2
Liu, J.C.3
Deng, T.4
Robinson, T.5
Chung, P.E.6
Wang, S.7
Herschkowitz, J.I.8
Egan, S.E.9
Perou, C.M.10
Zacksenhaus, E.11
-
110
-
-
79952668699
-
A nonfunctional retinoblastoma tumor suppressor (RB) pathway in premenopausal breast cancer is associated with resistance to tamoxifen
-
Lehn S, Ferno M, Jirstrom K, Ryden L, Landberg G. A nonfunctional retinoblastoma tumor suppressor (RB) pathway in premenopausal breast cancer is associated with resistance to tamoxifen. Cell Cycle. 2011; 10: 956-962.
-
(2011)
Cell Cycle
, vol.10
, pp. 956-962
-
-
Lehn, S.1
Ferno, M.2
Jirstrom, K.3
Ryden, L.4
Landberg, G.5
-
111
-
-
78650123930
-
RB in breast cancer: differential effects in estrogen receptor-positive and estrogen receptor-negative disease
-
Musgrove EA, Sutherland RL. RB in breast cancer: differential effects in estrogen receptor-positive and estrogen receptor-negative disease. Cell Cycle. 2010; 9: 4607-4615.
-
(2010)
Cell Cycle
, vol.9
, pp. 4607-4615
-
-
Musgrove, E.A.1
Sutherland, R.L.2
-
112
-
-
79958011689
-
A new therapeutic basis for treating Li-Fraumeni Syndrome breast tumors expressing mutated TP53
-
Glazer RI. A new therapeutic basis for treating Li-Fraumeni Syndrome breast tumors expressing mutated TP53. Oncotarget. 2010; 1: 470-471.
-
(2010)
Oncotarget
, vol.1
, pp. 470-471
-
-
Glazer, R.I.1
-
113
-
-
79953645997
-
A molecular signature of normal breast epithelial and stromal cells from Li-Fraumeni syndrome mutation carriers
-
Herbert BS, Chanoux RA, Liu Y, Baenziger PH, Goswami CP, McClintick JN, Edenberg HJ, Pennington RE, Lipkin SM, Kopelovich L. A molecular signature of normal breast epithelial and stromal cells from Li-Fraumeni syndrome mutation carriers. Oncotarget. 2010; 1: 405-422.
-
(2010)
Oncotarget
, vol.1
, pp. 405-422
-
-
Herbert, B.S.1
Chanoux, R.A.2
Liu, Y.3
Baenziger, P.H.4
Goswami, C.P.5
McClintick, J.N.6
Edenberg, H.J.7
Pennington, R.E.8
Lipkin, S.M.9
Kopelovich, L.10
-
114
-
-
74549166219
-
The POPX2 phosphatase regulates cancer cell motility and invasiveness
-
Susila A, Chan H, Loh AX, Phang HQ, Wong ET, Tergaonkar V, Koh CG. The POPX2 phosphatase regulates cancer cell motility and invasiveness. Cell Cycle. 2010; 9: 179-187.
-
(2010)
Cell Cycle
, vol.9
, pp. 179-187
-
-
Susila, A.1
Chan, H.2
Loh, A.X.3
Phang, H.Q.4
Wong, E.T.5
Tergaonkar, V.6
Koh, C.G.7
-
115
-
-
80053108088
-
BRCA1 A-complex fine tunes repair functions of BRCA1
-
Harris JL, Khanna KK. BRCA1 A-complex fine tunes repair functions of BRCA1. Aging. 2011; 3: 461-463.
-
(2011)
Aging
, vol.3
, pp. 461-463
-
-
Harris, J.L.1
Khanna, K.K.2
-
116
-
-
80053116010
-
Mutations in the BRCT binding site of BRCA1 result in hyper-recombination
-
Dever SM, Golding SE, Rosenberg E, Adams BR, Idowu MO, Quillin JM, Valerie N, Xu B, Povirk LF, Valerie K. Mutations in the BRCT binding site of BRCA1 result in hyper-recombination. Aging. 2011; 3: 515-532.
-
(2011)
Aging
, vol.3
, pp. 515-532
-
-
Dever, S.M.1
Golding, S.E.2
Rosenberg, E.3
Adams, B.R.4
Idowu, M.O.5
Quillin, J.M.6
Valerie, N.7
Xu, B.8
Povirk, L.F.9
Valerie, K.10
-
117
-
-
84055203847
-
Wiring the oncogenic circuitry: Pin1 unleashes mutant p53
-
Napoli M, Girardini JE, Piazza S, Del Sal G. Wiring the oncogenic circuitry: Pin1 unleashes mutant p53. Oncotarget. 2011; 2: 654-656,
-
(2011)
Oncotarget
, vol.2
, pp. 654-656
-
-
Napoli, M.1
Girardini, J.E.2
Piazza, S.3
Del Sal, G.4
-
118
-
-
80051741587
-
Network modeling of MDM2 inhibitoroxaliplatin combination reveals biological synergy in wtp53 solid tumors
-
Azmi AS, Banerjee S, Ali S, Wang Z, Bao B, Beck FW, Maitah M, Choi M, Shields TF, Philip PA, Sarkar FH, Mohammad RM. Network modeling of MDM2 inhibitoroxaliplatin combination reveals biological synergy in wtp53 solid tumors. Oncotarget. 2011; 2: 378-392.
-
(2011)
Oncotarget
, vol.2
, pp. 378-392
-
-
Azmi, A.S.1
Banerjee, S.2
Ali, S.3
Wang, Z.4
Bao, B.5
Beck, F.W.6
Maitah, M.7
Choi, M.8
Shields, T.F.9
Philip, P.A.10
Sarkar, F.H.11
Mohammad, R.M.12
-
119
-
-
77958510718
-
RB-pathway disruption in breast cancer: differential association with disease subtypes, diseasespecific prognosis and therapeutic response
-
Ertel A, Dean JL, Rui H, Liu C, Witkiewicz AK, Knudsen KE, Knudsen ES. RB-pathway disruption in breast cancer: differential association with disease subtypes, diseasespecific prognosis and therapeutic response. Cell Cycle. 2010; 9: 4153-4163.
-
(2010)
Cell Cycle
, vol.9
, pp. 4153-4163
-
-
Ertel, A.1
Dean, J.L.2
Rui, H.3
Liu, C.4
Witkiewicz, A.K.5
Knudsen, K.E.6
Knudsen, E.S.7
-
120
-
-
78650157692
-
BRCA1 modulates the expression of hnRNPA2B1 and KHSRP
-
Santarosa M, Del Col L, Viel A, Bivi N, D'Ambrosio C, Scaloni A, Tell G, Maestro R. BRCA1 modulates the expression of hnRNPA2B1 and KHSRP. Cell Cycle. 2010; 9: 4666-4673.
-
(2010)
Cell Cycle
, vol.9
, pp. 4666-4673
-
-
Santarosa, M.1
Del Col, L.2
Viel, A.3
Bivi, N.4
D'Ambrosio, C.5
Scaloni, A.6
Tell, G.7
Maestro, R.8
-
121
-
-
77953626325
-
Cell cycle proteins in epithelial cell differentiation: implications for breast cancer
-
Caldon CE, Sutherland RL, Musgrove E. Cell cycle proteins in epithelial cell differentiation: implications for breast cancer. Cell Cycle. 2010; 9: 1918-1928.
-
(2010)
Cell Cycle
, vol.9
, pp. 1918-1928
-
-
Caldon, C.E.1
Sutherland, R.L.2
Musgrove, E.3
-
122
-
-
79851479816
-
MicroRNA expression analysis in triple-negative (ER PR and Her2/neu) breast cancer
-
Radojicic J, Zaravinos A, Vrekoussis T, Kafousi M, Spandidos DA. Stathopoulos EN. MicroRNA expression analysis in triple-negative (ER, PR and Her2/neu) breast cancer. Cell Cycle. 2011; 10: 507-517.
-
(2011)
Cell Cycle
, vol.10
, pp. 507-517
-
-
Radojicic, J.1
Zaravinos, A.2
Vrekoussis, T.3
Kafousi, M.4
Spandidos, D.A.5
Stathopoulos, E.N.6
-
123
-
-
79951893051
-
MiRegulators in cancer stem cells of solid tumors
-
Ma S, Guan XY. MiRegulators in cancer stem cells of solid tumors. Cell Cycle. 2011; 10: 571-572.
-
(2011)
Cell Cycle
, vol.10
, pp. 571-572
-
-
Ma, S.1
Guan, X.Y.2
-
124
-
-
77953554439
-
miR-31: a crucial overseer of tumor metastasis and other emerging roles
-
Valastyan S, Weinberg RA. miR-31: a crucial overseer of tumor metastasis and other emerging roles. Cell Cycle. 2010; 9: 2124-2129.
-
(2010)
Cell Cycle
, vol.9
, pp. 2124-2129
-
-
Valastyan, S.1
Weinberg, R.A.2
-
125
-
-
84863187225
-
Epigenetic control of an oncogenic microRNA, miR-155, by BRCA1
-
Chang S, Sharan SK. Epigenetic control of an oncogenic microRNA, miR-155, by BRCA1. Oncotarget. 2012; 3: 5-6.
-
(2012)
Oncotarget.
, vol.3
, pp. 5-6
-
-
Chang, S.1
Sharan, S.K.2
-
126
-
-
77953150072
-
The TGFbeta-Par6 polarity pathway: linking the Par complex to EMT and breast cancer progression
-
Viloria-Petit AM, Wrana JL. The TGFbeta-Par6 polarity pathway: linking the Par complex to EMT and breast cancer progression. Cell Cycle. 2010; 9: 623-624.
-
(2010)
Cell Cycle.
, vol.9
, pp. 623-624
-
-
Viloria-Petit, A.M.1
Wrana, J.L.2
-
127
-
-
80052423435
-
Tracking the intermediate stages of epithelial-mesenchymal transition in epithelial stem cells and cancer
-
Jordan NV, Johnson GL, Abell AN. Tracking the intermediate stages of epithelial-mesenchymal transition in epithelial stem cells and cancer. Cell Cycle. 2011; 10: 2865-2873.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2865-2873
-
-
Jordan, N.V.1
Johnson, G.L.2
Abell, A.N.3
-
128
-
-
78649872745
-
Metformin against TGFbeta-induced epithelial-to-mesenchymal transition (EMT): from cancer stem cells to aging-associated fibrosis
-
Cufi S. Vazquez-Martin A, Oliveras-Ferraros C, Martin-Castillo B, Joven J, Menendez JA. Metformin against TGFbeta-induced epithelial-to-mesenchymal transition (EMT): from cancer stem cells to aging-associated fibrosis. Cell Cycle. 2010; 9: 4461-4468.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4461-4468
-
-
Cufi, S.1
Vazquez-Martin, A.2
Oliveras-Ferraros, C.3
Martin-Castillo, B.4
Joven, J.5
Menendez, J.A.6
-
129
-
-
77957005003
-
Metformin regulates breast cancer stem cell ontogeny by transcriptional regulation of the epithelial-mesenchymal transition (EMT) status
-
Vazquez-Martin A, Oliveras-Ferraros C, Cufi S, Del Barco S, Martin-Castillo B, Menendez JA. Metformin regulates breast cancer stem cell ontogeny by transcriptional regulation of the epithelial-mesenchymal transition (EMT) status. Cell Cycle. 2010; 9: 3807-3814.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3807-3814
-
-
Vazquez-Martin, A.1
Oliveras-Ferraros, C.2
Cufi, S.3
Del Barco, S.4
Martin-Castillo, B.5
Menendez, J.A.6
-
130
-
-
79959260166
-
Detecting and targeting mesenchymal-like subpopulations within squamous cell carcinomas
-
Basu D, Montone KT, Wang LP, Gimotty PA, Hammond R, Diehl JA, Rustgi AK, Lee JT, Rasanen K, Weinstein GS, Herlyn M. Detecting and targeting mesenchymal-like subpopulations within squamous cell carcinomas. Cell Cycle. 2011; 10: 2008-016.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2008-2016
-
-
Basu, D.1
Montone, K.T.2
Wang, L.P.3
Gimotty, P.A.4
Hammond, R.5
Diehl, J.A.6
Rustgi, A.K.7
Lee, J.T.8
Rasanen, K.9
Weinstein, G.S.10
Herlyn, M.11
-
131
-
-
79957998467
-
AKT1/BRCA1 in the control of homologous recombination and genetic stability: the missing link between hereditary and sporadic breast cancers
-
Guirouilh-Barbat JK, Wilhelm T, Lopez BS. AKT1/BRCA1 in the control of homologous recombination and genetic stability: the missing link between hereditary and sporadic breast cancers. Oncotarget. 2010; 1: 691-699.
-
(2010)
Oncotarget.
, vol.1
, pp. 691-699
-
-
Guirouilh-Barbat, J.K.1
Wilhelm, T.2
Lopez, B.S.3
-
132
-
-
84865865358
-
PinX1: a sought-after major tumor suppressor at human chromosome 8p23
-
Zhou XZ. PinX1: a sought-after major tumor suppressor at human chromosome 8p23. Oncotarget. 2011; 2: 810-819.
-
(2011)
Oncotarget.
, vol.2
, pp. 810-819
-
-
Zhou, X.Z.1
-
133
-
-
77956818209
-
Reversibility of pre-malignant estrogen-induced epigenetic changes
-
Kutanzi KR, Koturbash I, Kovalchuk O. Reversibility of pre-malignant estrogen-induced epigenetic changes. Cell Cycle. 2010; 9: 3078-3084.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3078-3084
-
-
Kutanzi, K.R.1
Koturbash, I.2
Kovalchuk, O.3
-
134
-
-
77956794619
-
MAD2 downregulation in hypoxia is independent of promoter hypermethylation
-
Prencipe M, McGoldrick A, Perry AS, O'Grady A, Phelan S, McGrogan B, Fitzpatrick P, Watson JA, Furlong F, Brennan DJ, Lawler M, Kay E, McCann A. MAD2 downregulation in hypoxia is independent of promoter hypermethylation. Cell Cycle. 2010; 9: 2856-2865.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2856-2865
-
-
Prencipe, M.1
Mcgoldrick, A.2
Perry, A.S.3
O'Grady, A.4
Phelan, S.5
Mcgrogan, B.6
Fitzpatrick, P.7
Watson, J.A.8
Furlong, F.9
Brennan, D.J.10
Lawler, M.11
Kay, E.12
McCann, A.13
-
135
-
-
77956399348
-
HIF1-alpha functions as a tumor promoter in cancer associated fibroblasts, and as a tumor suppressor in breast cancer cells: Autophagy drives compartment-specific oncogenesis
-
Chiavarina B, Whitaker-Menezes D, Migneco G, Martinez-Outschoorn UE, Pavlides S, Howell A, Tanowitz HB, Casimiro MC, Wang C, Pestell RG, Grieshaber P, Caro J, Sotgia F, Lisanti MP. HIF1-alpha functions as a tumor promoter in cancer associated fibroblasts, and as a tumor suppressor in breast cancer cells: Autophagy drives compartment-specific oncogenesis. Cell Cycle. 2010; 9: 3534-3551.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3534-3551
-
-
Chiavarina, B.1
Whitaker-Menezes, D.2
Migneco, G.3
Martinez-Outschoorn, U.E.4
Pavlides, S.5
Howell, A.6
Tanowitz, H.B.7
Casimiro, M.C.8
Wang, C.9
Pestell, R.G.10
Grieshaber, P.11
Caro, J.12
Sotgia, F.13
Lisanti, M.P.14
-
136
-
-
77956399968
-
The autophagic tumor stroma model of cancer: Role of oxidative stress and ketone production in fueling tumor cell metabolism
-
Pavlides S, Tsirigos A, Migneco G, Whitaker-Menezes D, Chiavarina B, Flomenberg N, Frank PG, Casimiro MC, Wang C, Pestell RG, Martinez-Outschoorn UE, Howell A, Sotgia F, Lisanti MP. The autophagic tumor stroma model of cancer: Role of oxidative stress and ketone production in fueling tumor cell metabolism. Cell Cycle. 2010; 9: 3485-3505.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3485-3505
-
-
Pavlides, S.1
Tsirigos, A.2
Migneco, G.3
Whitaker-Menezes, D.4
Chiavarina, B.5
Flomenberg, N.6
Frank, P.G.7
Casimiro, M.C.8
Wang, C.9
Pestell, R.G.10
Martinez-Outschoorn, U.E.11
Howell, A.12
Sotgia, F.13
Lisanti, M.P.14
-
137
-
-
77956400210
-
Autophagy in cancer associated fibroblasts promotes tumor cell survival: Role of hypoxia, HIF1 induction and NFkappaB activation in the tumor stromal microenvironment
-
Martinez-Outschoorn UE, Trimmer C, Lin Z, Whitaker-Menezes D, Chiavarina B, Zhou J, Wang C, Pavlides S, Martinez-Cantarin MP, Capozza F, Witkiewicz AK, Flomenberg N, Howell A, Pestell RG, Caro J, Lisanti MP, et al. Autophagy in cancer associated fibroblasts promotes tumor cell survival: Role of hypoxia, HIF1 induction and NFkappaB activation in the tumor stromal microenvironment. Cell Cycle. 2010; 9: 3515-3533.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3515-3533
-
-
Martinez-Outschoorn, U.E.1
Trimmer, C.2
Lin, Z.3
Whitaker-Menezes, D.4
Chiavarina, B.5
Zhou, J.6
Wang, C.7
Pavlides, S.8
Martinez-Cantarin, M.P.9
Capozza, F.10
Witkiewicz, A.K.11
Flomenberg, N.12
Howell, A.13
Pestell, R.G.14
Caro, J.15
Lisanti, M.P.16
-
138
-
-
77954155633
-
Transcriptional evidence for the "Reverse Warburg Effect" in human breast cancer tumor stroma and metastasis: similarities with oxidative stress, inflammation, Alzheimer's disease, and "Neuron-Glia Metabolic Coupling"
-
Pavlides S, Tsirigos A, Vera I, Flomenberg N, Frank PG, Casimiro MC, Wang C, Pestell RG, Martinez-Outschoorn UE, Howell A, Sotgia F, Lisanti MP. Transcriptional evidence for the "Reverse Warburg Effect" in human breast cancer tumor stroma and metastasis: similarities with oxidative stress, inflammation, Alzheimer's disease, and "Neuron-Glia Metabolic Coupling". Aging. 2010; 2: 185-199.
-
(2010)
Aging.
, vol.2
, pp. 185-199
-
-
Pavlides, S.1
Tsirigos, A.2
Vera, I.3
Flomenberg, N.4
Frank, P.G.5
Casimiro, M.C.6
Wang, C.7
Pestell, R.G.8
Martinez-Outschoorn, U.E.9
Howell, A.10
Sotgia, F.11
Lisanti, M.P.12
-
139
-
-
79957902168
-
Cytokine production and inflammation drive autophagy in the tumor microenvironment: role of stromal caveolin-1 as a key regulator
-
Martinez-Outschoorn UE, Whitaker-Menezes D, Lin Z, Flomenberg N, Howell A, Pestell RG, Lisanti MP, Sotgia F. Cytokine production and inflammation drive autophagy in the tumor microenvironment: role of stromal caveolin-1 as a key regulator. Cell Cycle. 2011; 10: 1784-1793.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1784-1793
-
-
Martinez-Outschoorn, U.E.1
Whitaker-Menezes, D.2
Lin, Z.3
Flomenberg, N.4
Howell, A.5
Pestell, R.G.6
Lisanti, M.P.7
Sotgia, F.8
-
140
-
-
84858310960
-
Defining bad stroma in human breast tumors
-
Howell A. Defining bad stroma in human breast tumors. Cell Cycle. 2011; 10: 3056.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3056
-
-
Howell, A.1
-
141
-
-
79957927705
-
Molecular profiling of a lethal tumor microenvironment, as defined by stromal caveolin-1 status in breast cancers
-
Witkiewicz AK, Kline J, Queenan M, Brody JR, Tsirigos A, Bilal E, Pavlides S, Ertel A, Sotgia F, Lisanti MP. Molecular profiling of a lethal tumor microenvironment, as defined by stromal caveolin-1 status in breast cancers. Cell Cycle. 2011; 10: 1794-1809.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1794-1809
-
-
Witkiewicz, A.K.1
Kline, J.2
Queenan, M.3
Brody, J.R.4
Tsirigos, A.5
Bilal, E.6
Pavlides, S.7
Ertel, A.8
Sotgia, F.9
Lisanti, M.P.10
-
142
-
-
79954537559
-
Ketones and lactate increase cancer cell "stemness," driving recurrence, metastasis and poor clinical outcome in breast cancer: achieving personalized medicine via Metabolo-Genomics
-
Martinez-Outschoorn UE, Prisco M, Ertel A, Tsirigos A, Lin Z, Pavlides S, Wang C, Flomenberg N, Knudsen ES, Howell A, Pestell RG, Sotgia F, Lisanti MP. Ketones and lactate increase cancer cell "stemness," driving recurrence, metastasis and poor clinical outcome in breast cancer: achieving personalized medicine via Metabolo-Genomics. Cell Cycle. 2011; 10: 1271-1286.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1271-1286
-
-
Martinez-Outschoorn, U.E.1
Prisco, M.2
Ertel, A.3
Tsirigos, A.4
Lin, Z.5
Pavlides, S.6
Wang, C.7
Flomenberg, N.8
Knudsen, E.S.9
Howell, A.10
Pestell, R.G.11
Sotgia, F.12
Lisanti, M.P.13
-
143
-
-
79951866285
-
Candidate pathways linking inducible nitric oxide synthase to a basal-like transcription pattern and tumor progression in human breast cancer
-
Ambs S, Glynn SA. Candidate pathways linking inducible nitric oxide synthase to a basal-like transcription pattern and tumor progression in human breast cancer. Cell Cycle. 2011; 10: 619-624.
-
(2011)
Cell Cycle.
, vol.10
, pp. 619-624
-
-
Ambs, S.1
Glynn, S.A.2
-
144
-
-
77955750366
-
Overexpression of the RNA binding protein HuR impairs tumor growth in triple negative breast cancer associated with deficient angiogenesis
-
Gubin MM, Calaluce R, Davis JW, Magee JD, Strouse CS, Shaw DP, Ma L, Brown A, Hoffman T, Rold TL, Atasoy U. Overexpression of the RNA binding protein HuR impairs tumor growth in triple negative breast cancer associated with deficient angiogenesis. Cell Cycle. 2010; 9: 3337-3346.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3337-3346
-
-
Gubin, M.M.1
Calaluce, R.2
Davis, J.W.3
Magee, J.D.4
Strouse, C.S.5
Shaw, D.P.6
Ma, L.7
Brown, A.8
Hoffman, T.9
Rold, T.L.10
Atasoy, U.11
-
145
-
-
77955731695
-
HdmX overexpression inhibits oncogene induced cellular senescence
-
Miller KR, Kelley K, Tuttle R, Berberich SJ. HdmX overexpression inhibits oncogene induced cellular senescence. Cell Cycle. 2010; 9: 3376-3382.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3376-3382
-
-
Miller, K.R.1
Kelley, K.2
Tuttle, R.3
Berberich, S.J.4
-
146
-
-
80052879467
-
δNp63alpha promotes cellular quiescence via induction and activation of Notch3
-
Kent S, Hutchinson J, Balboni A, Decastro A, Cherukuri P, Direnzo J. δNp63alpha promotes cellular quiescence via induction and activation of Notch3. Cell Cycle. 2011; 10: 3111-3118.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3111-3118
-
-
Kent, S.1
Hutchinson, J.2
Balboni, A.3
Decastro, A.4
Cherukuri, P.5
Direnzo, J.6
-
147
-
-
84874765711
-
Mechanisms of acquired resistance to ERK1/2 pathway inhibitors
-
In Press
-
Little AS, Smith PD, Cook SJ. Mechanisms of acquired resistance to ERK1/2 pathway inhibitors. Oncogene. 2012; In Press.
-
(2012)
Oncogene
-
-
Little, A.S.1
Smith, P.D.2
Cook, S.J.3
-
148
-
-
79953240219
-
Amplification of the driving oncogene, KRAS or BRAF, underpins acquired resistance to MEK1/2 inhibitors in colorectal cancer cells
-
Little S, Balmanno K, Sale MJ, Newman S, Dry JR, Hampson M, Edwards PAW, Smith PD, Cook SJ. Amplification of the driving oncogene, KRAS or BRAF, underpins acquired resistance to MEK1/2 inhibitors in colorectal cancer cells. Sci Signal. 2011; 4:ra17
-
(2011)
Sci Signal
, vol.4
-
-
Little, S.1
Balmanno, K.2
Sale, M.J.3
Newman, S.4
Dry, J.R.5
Hampson, M.6
Edwards, P.A.W.7
Smith, P.D.8
Cook, S.J.9
-
149
-
-
84862726767
-
ERK inhibition overcomes acquired resistance to MEK inhibitors
-
Hatzivassiliou G, Liu B, O'Brien C, Spoerke JM, Hoeflich KP, Haverty PM, Soriano R, Forrest WF, Heldens S, Chen H, Toy K, Ha C, Zhou W, Song K, Friedman LS, Amler LC, et al. ERK inhibition overcomes acquired resistance to MEK inhibitors. Mol Cancer Ther. 2012; 11: 1143-1154.
-
(2012)
Mol Cancer Ther.
, vol.11
, pp. 1143-1154
-
-
Hatzivassiliou, G.1
Liu, B.2
O'Brien, C.3
Spoerke, J.M.4
Hoeflich, K.P.5
Haverty, P.M.6
Soriano, R.7
Forrest, W.F.8
Heldens, S.9
Chen, H.10
Toy, K.11
Ha, C.12
Zhou, W.13
Song, K.14
Friedman, L.S.15
Amler, L.C.16
-
150
-
-
84859627981
-
MEK inhibition enhances ABT-737-induced leukemia cell apoptosis via prevention of ERK-activated MCL-1 induction and modulation of MCL-1/BIM complex
-
Konopleva M, Milella M, Ruvolo P, Watts JC, Ricciardi MR, Korchin B, McQueen T, Bornmann W, Tsao T, Bergamo P, Mak DH, Chen W, McCubrey J, Tafuri A, Andreeff M. MEK inhibition enhances ABT-737-induced leukemia cell apoptosis via prevention of ERK-activated MCL-1 induction and modulation of MCL-1/BIM complex. Leukemia. 2012; 26: 778-87.
-
(2012)
Leukemia
, vol.26
, pp. 778-787
-
-
Konopleva, M.1
Milella, M.2
Ruvolo, P.3
Watts, J.C.4
Ricciardi, M.R.5
Korchin, B.6
Mcqueen, T.7
Bornmann, W.8
Tsao, T.9
Bergamo, P.10
Mak, D.H.11
Chen, W.12
Mccubrey, J.13
Tafuri, A.14
Andreeff, M.15
-
151
-
-
84867328500
-
Therapeutic potential of MEK inhibition in acute myelogenous leukemia: rationale for "vertical" and "lateral" combination strategies
-
Ricciardi MR, Scerpa MC, Bergamo P, Ciuffreda L, Petrucci MT, Chiaretti S, Tavolaro S, Mascolo MG, Abrams SL, Steelman LS, Tsao T, Marchetti A, Konopleva M, Del Bufalo D, Cognetti F, Foà R, et al. Therapeutic potential of MEK inhibition in acute myelogenous leukemia: rationale for "vertical" and "lateral" combination strategies. J Mol Med (Berl). 2012; 90: 1133-1144.
-
(2012)
J Mol Med (Berl).
, vol.90
, pp. 1133-1144
-
-
Ricciardi, M.R.1
Scerpa, M.C.2
Bergamo, P.3
Ciuffreda, L.4
Petrucci, M.T.5
Chiaretti, S.6
Tavolaro, S.7
Mascolo, M.G.8
Abrams, S.L.9
Steelman, L.S.10
Tsao, T.11
Marchetti, A.12
Konopleva, M.13
Del Bufalo, D.14
Cognetti, F.15
Foà, R.16
-
152
-
-
70350066163
-
Structure-guided design of potent and selective pyrimidylpyrrole inhibitors of extracellular signalregulated kinase (ERK) using conformational control
-
Aronov AM, Tang Q, Martinez-Botella G, Bemis GW, Cao J, Chen G, Ewing NP, Ford PJ, Germann UA, Green J, Hale MR, Jacobs M, Janetka JW, Maltais F, Markland W, Namchuk MN, et al. Structure-guided design of potent and selective pyrimidylpyrrole inhibitors of extracellular signalregulated kinase (ERK) using conformational control. J Med Chem. 2009; 52: 6362-6368.
-
(2009)
J Med Chem.
, vol.52
, pp. 6362-6368
-
-
Aronov, A.M.1
Tang, Q.2
Martinez-Botella, G.3
Bemis, G.W.4
Cao, J.5
Chen, G.6
Ewing, N.P.7
Ford, P.J.8
Germann, U.A.9
Green, J.10
Hale, M.R.11
Jacobs, M.12
Janetka, J.W.13
Maltais, F.14
Markland, W.15
Namchuk, M.N.16
-
153
-
-
3042743988
-
Akt/protein kinase B signaling inhibitor-2, a selective small molecule inhibitor of Akt signaling with antitumor activity in cancer cells overexpressing Akt
-
Yang L, Dan HC, Sun M, Liu Q, Sun XM, Feldman RI, Hamilton AD, Polokoff M, Nicosia SV, Herlyn M, Sebti SM, Cheng JQ. Akt/protein kinase B signaling inhibitor-2, a selective small molecule inhibitor of Akt signaling with antitumor activity in cancer cells overexpressing Akt. Cancer Res. 2004; 64: 4394-4399.
-
(2004)
Cancer Res.
, vol.64
, pp. 4394-4399
-
-
Yang, L.1
Dan, H.C.2
Sun, M.3
Liu, Q.4
Sun, X.M.5
Feldman, R.I.6
Hamilton, A.D.7
Polokoff, M.8
Nicosia, S.V.9
Herlyn, M.10
Sebti, S.M.11
Cheng, J.Q.12
-
154
-
-
50449097578
-
Proapoptotic activity and chemosensitizing effect of the novel Akt inhibitor (2S)-1-(1H-Indol-3-yl)-3-[5-(3-methyl-2H-indazol-5-yl)pyridin-3-yl]oxypropan2-amine (A443654) in T acute lymphoblastic leukemia
-
Fala F, Blalock WL, Tazzari P, Cappellini A, Chiarini F, Martinelli G, Tafuri A, McCubrey JA, Cocco L, Martelli AM. Proapoptotic activity and chemosensitizing effect of the novel Akt inhibitor (2S)-1-(1H-Indol-3-yl)-3-[5-(3-methyl-2H-indazol-5-yl)pyridin-3-yl]oxypropan2-amine (A443654) in T acute lymphoblastic leukemia. Molecular Pharmacology. 2008; 74: 884-895.
-
(2008)
Molecular Pharmacology.
, vol.74
, pp. 884-895
-
-
Fala, F.1
Blalock, W.L.2
Tazzari, P.3
Cappellini, A.4
Chiarini, F.5
Martinelli, G.6
Tafuri, A.7
McCubrey, J.A.8
Cocco, L.9
Martelli, A.M.10
-
155
-
-
33645085614
-
The Akt inhibitor KP372-1 inhibits proliferation and induces apoptosis and anoikis in squamous cell carcinoma of the head and neck
-
Mandal M, Younes M, Swan EA, Jasser SA, Doan D, Yigitbasi O, McMurphey A, Ludwick J, El-Naggar AK, Bucana C, Mills GB, Myers JN. The Akt inhibitor KP372-1 inhibits proliferation and induces apoptosis and anoikis in squamous cell carcinoma of the head and neck. Oral Oncol. 2006; 42: 430-439.
-
(2006)
Oral Oncol.
, vol.42
, pp. 430-439
-
-
Mandal, M.1
Younes, M.2
Swan, E.A.3
Jasser, S.A.4
Doan, D.5
Yigitbasi, O.6
McMurphey, A.7
Ludwick, J.8
El-Naggar, A.K.9
Bucana, C.10
Mills, G.B.11
Myers, J.N.12
-
156
-
-
56449084185
-
Synergistic proapoptotic activity of recombinant trail plus the akt inhibitor perifosine in acute myelogenous leukemia cells
-
Tazzari PL, Tabellini G, Ricci F, Papa V, Bortul R, Chiarini F, Evangelisti C, Martinelli G, Bontadini A, Cocco L, McCubrey JA, Martelli AM. Synergistic proapoptotic activity of recombinant trail plus the akt inhibitor perifosine in acute myelogenous leukemia cells. Cancer Res. 2008; 68: 9394-9403.
-
(2008)
Cancer Res.
, vol.68
, pp. 9394-9403
-
-
Tazzari, P.L.1
Tabellini, G.2
Ricci, F.3
Papa, V.4
Bortul, R.5
Chiarini, F.6
Evangelisti, C.7
Martinelli, G.8
Bontadini, A.9
Cocco, L.10
Mccubrey, J.A.11
Martelli, A.M.12
-
157
-
-
84868614691
-
Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: Eliminating activity by targeting at different levels
-
In Press
-
Bressanin D, Evangelisti C, Ricci F, Tabellini G, Chiarini F, Tazzari PL, Melchionda F, Buontempo F, Pagliaro P, Pession A, McCubrey JA, Martelli AM. Harnessing the PI3K/Akt/mTOR pathway in T-cell acute lymphoblastic leukemia: Eliminating activity by targeting at different levels. Oncotarget. 2012; In Press.
-
(2012)
Oncotarget.
-
-
Bressanin, D.1
Evangelisti, C.2
Ricci, F.3
Tabellini, G.4
Chiarini, F.5
Tazzari, P.L.6
Melchionda, F.7
Buontempo, F.8
Pagliaro, P.9
Pession, A.10
McCubrey, J.A.11
Martelli, A.M.12
-
158
-
-
72449198506
-
Preoperative therapy for early-stage NSCLC: oppurtunities and challenges
-
Owonikoko T, Khuri ER, Ramalingam SS. Preoperative therapy for early-stage NSCLC: oppurtunities and challenges. Oncology. 2009; 23: 886-892.
-
(2009)
Oncology.
, vol.23
, pp. 886-892
-
-
Owonikoko, T.1
Khuri, E.R.2
Ramalingam, S.S.3
-
159
-
-
74849095946
-
Targeting translation in acute myeloid leukemia: a new paradigm for therapy?
-
Tamburini J, Green AS, Chapuis N, Bardet V, Lacombe C, Mayeux P, Bouscary D. Targeting translation in acute myeloid leukemia: a new paradigm for therapy? Cell Cycle. 2009; 8: 3893-3899.
-
(2009)
Cell Cycle
, vol.8
, pp. 3893-3899
-
-
Tamburini, J.1
Green, A.S.2
Chapuis, N.3
Bardet, V.4
Lacombe, C.5
Mayeux, P.6
Bouscary, D.7
-
161
-
-
36049023679
-
Phase I study of Everolimus in pediatric patients with refractory solid tumors
-
Fouladi M, Laningham F, Wu J, O'Shaughnessy MA, Molina K, Broniscer A, Spunt SL, Luckett I, Stewart CF, Houghton PJ, Gilbertson RJ, Furman WL. Phase I study of Everolimus in pediatric patients with refractory solid tumors. JCO. 2007; 25: 4806-4812.
-
(2007)
JCO.
, vol.25
, pp. 4806-4812
-
-
Fouladi, M.1
Laningham, F.2
Wu, J.3
O'Shaughnessy, M.A.4
Molina, K.5
Broniscer, A.6
Spunt, S.L.7
Luckett, I.8
Stewart, C.F.9
Houghton, P.J.10
Gilbertson, R.J.11
Furman, W.L.12
-
162
-
-
0029965452
-
Wortmannin inactivates phosphoinositide 3-kinase by covalent modification of Lys-802, a residue involved in the phosphate transfer reaction
-
Wymann MP, Bulgarelli-Leva G, Zvelebil MJ, Pirola L, Vanhaesebroeck B, Waterfield MD, Panayotou G. Wortmannin inactivates phosphoinositide 3-kinase by covalent modification of Lys-802, a residue involved in the phosphate transfer reaction. Mol Cell Biol. 1996; 16: 1722-1733.
-
(1996)
Mol Cell Biol.
, vol.16
, pp. 1722-1733
-
-
Wymann, M.P.1
Bulgarelli-Leva, G.2
Zvelebil, M.J.3
Pirola, L.4
Vanhaesebroeck, B.5
Waterfield, M.D.6
Panayotou, G.7
-
163
-
-
0028170210
-
A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002)
-
Vlahos CJ, Matter WF, Hui KY, Brown RF. A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002). J Biol Chem. 1994; 269: 5241-5248.
-
(1994)
J Biol Chem.
, vol.269
, pp. 5241-5248
-
-
Vlahos, C.J.1
Matter, W.F.2
Hui, K.Y.3
Brown, R.F.4
-
164
-
-
34247339936
-
Exploring the specificity of the PI3K family inhibitor LY294002
-
Gharbi SI, Zvelebil MJ, Shuttleworth SJ, Hancox T, Saghir N, Timms JF, Waterfield MD. Exploring the specificity of the PI3K family inhibitor LY294002. Biochem J. 2007; 404: 15-21.
-
(2007)
Biochem J.
, vol.404
, pp. 15-21
-
-
Gharbi, S.I.1
Zvelebil, M.J.2
Shuttleworth, S.J.3
Hancox, T.4
Saghir, N.5
Timms, J.F.6
Waterfield, M.D.7
-
165
-
-
51849098272
-
Drug discovery approaches targeting the PI3K/Akt pathway in cancer
-
Garcia-Echeverria C, Sellers WR. Drug discovery approaches targeting the PI3K/Akt pathway in cancer. Oncogene. 2008; 27: 5511-5526.
-
(2008)
Oncogene.
, vol.27
, pp. 5511-5526
-
-
Garcia-Echeverria, C.1
Sellers, W.R.2
-
166
-
-
78349265690
-
Laminin regulates PI3K basal localization and activation to sustain STAT5 activation
-
Xu R, Spencer VA, Groesser DL, Bissell MJ. Laminin regulates PI3K basal localization and activation to sustain STAT5 activation. Cell Cycle. 2010; 9: 4315-4322.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4315-4322
-
-
Xu, R.1
Spencer, V.A.2
Groesser, D.L.3
Bissell, M.J.4
-
167
-
-
74949132928
-
The EphB2 tumor suppressor induces autophagic cell death via concomitant activation of the ERK1/2 and PI3K pathways
-
Kandouz M, Haidara K, Zhao J, Brisson ML, Batist G. The EphB2 tumor suppressor induces autophagic cell death via concomitant activation of the ERK1/2 and PI3K pathways. Cell Cycle. 2010; 9: 398-407.
-
(2010)
Cell Cycle.
, vol.9
, pp. 398-407
-
-
Kandouz, M.1
Haidara, K.2
Zhao, J.3
Brisson, M.L.4
Batist, G.5
-
168
-
-
79952355101
-
Ionizing radiation-induced TAp63alpha phosphorylation at C-terminal S/TQ motifs requires the N-terminal transactivation (TA) domain
-
Kim DA, Lee BL, Suh EK. Ionizing radiation-induced TAp63alpha phosphorylation at C-terminal S/TQ motifs requires the N-terminal transactivation (TA) domain. Cell Cycle. 2011; 10: 840-849.
-
(2011)
Cell Cycle.
, vol.10
, pp. 840-849
-
-
Kim, D.A.1
Lee, B.L.2
Suh, E.K.3
-
169
-
-
79951900140
-
Nek1 kinasefunctions in DNA damage response and checkpoint control through a pathway independent of ATM and ATR
-
Chen Y, Chen CF, Riley DJ, Chen PL. Nek1 kinasefunctions in DNA damage response and checkpoint control through a pathway independent of ATM and ATR. Cell Cycle. 2011; 10: 655-663.
-
(2011)
Cell Cycle.
, vol.10
, pp. 655-663
-
-
Chen, Y.1
Chen, C.F.2
Riley, D.J.3
Chen, P.L.4
-
170
-
-
83755186554
-
Yeast-like chronological senescence in mammalian cells: phenomenon, mechanism and pharmacological suppression
-
Leontieva OV, Blagosklonny MV. Yeast-like chronological senescence in mammalian cells: phenomenon, mechanism and pharmacological suppression. Aging. 2011; 3: 1078-1091.
-
(2011)
Aging.
, vol.3
, pp. 1078-1091
-
-
Leontieva, O.V.1
Blagosklonny, M.V.2
-
171
-
-
4444223702
-
Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling
-
Ihle NT, Williams R, Chow S, Chew W, Berggren MI, Paine-Murrieta G, Minion DJ, Halter RJ, Wipf P, Abraham R, Kirkpatrick L, Powis G. Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling. Mol Cancer Ther. 2004; 3: 763-772.
-
(2004)
Mol Cancer Ther.
, vol.3
, pp. 763-772
-
-
Ihle, N.T.1
Williams, R.2
Chow, S.3
Chew, W.4
Berggren, M.I.5
Paine-Murrieta, G.6
Minion, D.J.7
Halter, R.J.8
Wipf, P.9
Abraham, R.10
Kirkpatrick, L.11
Powis, G.12
-
172
-
-
77956004085
-
Cellular and in vivo activity of a novel PI3K inhibitor, PX-866, against human glioblastoma
-
Koul D, Shen R, Kim YW, Kondo Y, Lu Y, Bankson J, Ronen SM, Kirkpatrick DL, Powis G, Yung WK. Cellular and in vivo activity of a novel PI3K inhibitor, PX-866, against human glioblastoma. Neuro Oncol. 2010; 12: 559-569.
-
(2010)
Neuro Oncol.
, vol.12
, pp. 559-569
-
-
Koul, D.1
Shen, R.2
Kim, Y.W.3
Kondo, Y.4
Lu, Y.5
Bankson, J.6
Ronen, S.M.7
Kirkpatrick, D.L.8
Powis, G.9
Yung, W.K.10
-
173
-
-
83155165424
-
GDC-0941 inhibits metastatic characteristics of thyroid carcinomas by targeting both the phosphoinositide-3 kinase (PI3K) and hypoxiainducible factor-1-alpha (HIF-1-alpha) pathways
-
Burrows N, Babur M, Resch J, Ridsdale S, Mejin M, Rowling EJ, Brabant G, Williams KJ. GDC-0941 inhibits metastatic characteristics of thyroid carcinomas by targeting both the phosphoinositide-3 kinase (PI3K) and hypoxiainducible factor-1-alpha (HIF-1-alpha) pathways. J Clin Endocrinol Metab. 2011; 96: E1934-1943.
-
(2011)
J Clin Endocrinol Metab.
, vol.96
-
-
Burrows, N.1
Babur, M.2
Resch, J.3
Ridsdale, S.4
Mejin, M.5
Rowling, E.J.6
Brabant, G.7
Williams, K.J.8
-
174
-
-
84862907761
-
The novel dual PI3K/mTOR inhibitor GDC-0941 synergizes with the MEK inhibitor U0126 in non-small cell lung cancer cells
-
Zou ZQ, Zhang LN, Wang F, Bellenger J, Shen YZ, Zhang XH. The novel dual PI3K/mTOR inhibitor GDC-0941 synergizes with the MEK inhibitor U0126 in non-small cell lung cancer cells. Mol Med Report. 2012; 5: 503-508.
-
(2012)
Mol Med Report.
, vol.5
, pp. 503-508
-
-
Zou, Z.Q.1
Zhang, L.N.2
Wang, F.3
Bellenger, J.4
Shen, Y.Z.5
Zhang, X.H.6
-
175
-
-
22544444889
-
Essential role for the p110d isoform in phosphoinositide 3-kinase activation and cell proliferation in acute myeloid leukemia
-
Sujobert P, Bardet V, Cornillet-Lefebvre P, Hayflick JS, Prie N, Verdier F, Vanhaesebroeck B, Muller O, Pesce F, Ifrah N, Hunault-Berger M, Berthou C, Villemagne B, Jourdan E, Audhuy B, Solary E, et al. Essential role for the p110d isoform in phosphoinositide 3-kinase activation and cell proliferation in acute myeloid leukemia. Blood. 2005; 106: 1063-1066.
-
(2005)
Blood.
, vol.106
, pp. 1063-1066
-
-
Sujobert, P.1
Bardet, V.2
Cornillet-Lefebvre, P.3
Hayflick, J.S.4
Prie, N.5
Verdier, F.6
Vanhaesebroeck, B.7
Muller, O.8
Pesce, F.9
Ifrah, N.10
Hunault-Berger, M.11
Berthou, C.12
Villemagne, B.13
Jourdan, E.14
Audhuy, B.15
Solary, E.16
-
176
-
-
33750459743
-
A selective inhibitor of the p110d isoform of PI 3-kinase inhibits AML cell proliferation and survival and increases the cytotoxic effects of VP16
-
Billottet C, Grandage VL, Gale RE, Quattropani A, Rommel C, Vanhaesebroeck B, Khwaja A. A selective inhibitor of the p110d isoform of PI 3-kinase inhibits AML cell proliferation and survival and increases the cytotoxic effects of VP16. Oncogene. 2006; 25: 6648-6659.
-
(2006)
Oncogene.
, vol.25
, pp. 6648-6659
-
-
Billottet, C.1
Grandage, V.L.2
Gale, R.E.3
Quattropani, A.4
Rommel, C.5
Vanhaesebroeck, B.6
Khwaja, A.7
-
177
-
-
38049187096
-
Mammalian target of rapamycin (mTOR) inhibition activates phosphatidylinositol 3-kinase/Akt by up-regulating insulin-like growth factor-1 receptor signaling in acute myeloid leukemia: rationale for therapeutic inhibition of both pathways
-
Tamburini J, Chapuis N, Bardet V, Park S, Sujobert P, Willems L, Ifrah N, Dreyfus F, Mayeux P, Lacombe C, Bouscary D. Mammalian target of rapamycin (mTOR) inhibition activates phosphatidylinositol 3-kinase/Akt by up-regulating insulin-like growth factor-1 receptor signaling in acute myeloid leukemia: rationale for therapeutic inhibition of both pathways. Blood. 2008; 111: 379-382.
-
(2008)
Blood.
, vol.111
, pp. 379-382
-
-
Tamburini, J.1
Chapuis, N.2
Bardet, V.3
Park, S.4
Sujobert, P.5
Willems, L.6
Ifrah, N.7
Dreyfus, F.8
Mayeux, P.9
Lacombe, C.10
Bouscary, D.11
-
178
-
-
75349110785
-
PI(3) kinases: revealing the delta lady
-
Workman P, van Montfort RL. PI(3) kinases: revealing the delta lady. Nat Chem Biol. 2010; 6: 82-83.
-
(2010)
Nat Chem Biol.
, vol.6
, pp. 82-83
-
-
Workman, P.1
van Montfort, R.L.2
-
180
-
-
75349106113
-
The p110 delta structure: mechanisms for selectivity and potency of new PI(3)K inhibitors
-
Berndt A, Miller S, Williams O, Le DD, Houseman BT, Pacold JI, Gorrec F, Hon WC, Liu Y, Rommel C, Gaillard P, Rückle T, Schwarz MK, Shokat KM, Shaw JP, Williams RL. The p110 delta structure: mechanisms for selectivity and potency of new PI(3)K inhibitors. Nat Chem Biol. 2010; 6: 117-124.
-
(2010)
Nat Chem Biol.
, vol.6
, pp. 117-124
-
-
Berndt, A.1
Miller, S.2
Williams, O.3
Le, D.D.4
Houseman, B.T.5
Pacold, J.I.6
Gorrec, F.7
Hon, W.C.8
Liu, Y.9
Rommel, C.10
Gaillard, P.11
Rückle, T.12
Schwarz, M.K.13
Shokat, K.M.14
Shaw, J.P.15
Williams, R.L.16
-
181
-
-
78751553221
-
CAL-101, a p110d selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability
-
Lannutti BJ, Meadows SA, Herman SE, Kashishian A, Steiner B, Johnson AJ, Byrd C, Tyner JW, Loriaux MM, Deininger M, Druker BJ, Puri KD, Ulrich RG, Giese NA. CAL-101, a p110d selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability. Blood. 2011; 117: 591-594.
-
(2011)
Blood.
, vol.117
, pp. 591-594
-
-
Lannutti, B.J.1
Meadows, S.A.2
Herman, S.E.3
Kashishian, A.4
Steiner, B.5
Johnson, A.J.6
Byrd, C.7
Tyner, J.W.8
Loriaux, M.M.9
Deininger, M.10
Druker, B.J.11
Puri, K.D.12
Ulrich, R.G.13
Giese, N.A.14
-
182
-
-
84863116183
-
PI3K-delta inhibitor, GS-1101 (CAL-101), attenuates pathway signaling, induces apoptosis, and overcomes signals from the microenvironment in cellular models of Hodgkin lymphoma
-
Meadows SA, Vega F, Kashishian A, Johnson D, Diehl V, Miller LL, Younes A, Lannutti BJ. PI3K-delta inhibitor, GS-1101 (CAL-101), attenuates pathway signaling, induces apoptosis, and overcomes signals from the microenvironment in cellular models of Hodgkin lymphoma. Blood. 2012; 119: 1897-1900
-
(2012)
Blood.
, vol.119
, pp. 1897-1900
-
-
Meadows, S.A.1
Vega, F.2
Kashishian, A.3
Johnson, D.4
Diehl, V.5
Miller, L.L.6
Younes, A.7
Lannutti, B.J.8
-
183
-
-
77749264641
-
28th Annual JP Morgan healthcare conference-Exelixis and Nektar therapeutics
-
Gale S, Croasdell G. 28th Annual JP Morgan healthcare conference-Exelixis and Nektar therapeutics. IDrugs. 2010; 13: 139-141.
-
(2010)
IDrugs.
, vol.13
, pp. 139-141
-
-
Gale, S.1
Croasdell, G.2
-
184
-
-
84856826293
-
Identification and characterization of NVP-BKM120, an orally available pan-class I PI3-kinase inhibitor
-
Maira SM, Pecchi S, Huang A, Burger M, Knapp M, Sterker D, Schnell C, Guthy D, Nagel T, Wiesmann M, Brachmann S, Fritsch C, Dorsch M, Chène P, Shoemaker K, De Pover A, et al. Identification and characterization of NVP-BKM120, an orally available pan-class I PI3-kinase inhibitor. Mol Cancer Ther. 2012; 11: 317-328.
-
(2012)
Mol Cancer Ther.
, vol.11
, pp. 317-328
-
-
Maira, S.M.1
Pecchi, S.2
Huang, A.3
Burger, M.4
Knapp, M.5
Sterker, D.6
Schnell, C.7
Guthy, D.8
Nagel, T.9
Wiesmann, M.10
Brachmann, S.11
Fritsch, C.12
Dorsch, M.13
Chène, P.14
Shoemaker, K.15
De Pover, A.16
-
185
-
-
84856071447
-
Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors
-
Bendell JC, Rodon J, Burris HA, de Jonge M, Verweij J, Birle D, Demanse D, De Buck SS, Ru QC, Peters M, Goldbrunner M, Baselga J. Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors. J Clin Oncol. 2012; 30: 282-290.
-
(2012)
J Clin Oncol.
, vol.30
, pp. 282-290
-
-
Bendell, J.C.1
Rodon, J.2
Burris, H.A.3
de Jonge, M.4
Verweij, J.5
Birle, D.6
Demanse, D.7
De Buck, S.S.8
Ru, Q.C.9
Peters, M.10
Goldbrunner, M.11
Baselga, J.12
-
186
-
-
84859876030
-
Will PI3K pathway inhibitors be effective as single agents in patients with cancer?
-
Garrett JT, Chakrabarty A, Arteaga CL. Will PI3K pathway inhibitors be effective as single agents in patients with cancer? Oncotarget. 2011; 2: 1314-1321.
-
(2011)
Oncotarget
, vol.2
, pp. 1314-1321
-
-
Garrett, J.T.1
Chakrabarty, A.2
Arteaga, C.L.3
-
188
-
-
62549160588
-
First in class, first in human phase I results of targeted agents: highlights of the 2008 American Society of Clinical Oncology meeting
-
Molckovsky A, Siu LL. First in class, first in human phase I results of targeted agents: highlights of the 2008 American Society of Clinical Oncology meeting. J Hematol Oncol. 2008; 1: 20.
-
(2008)
J Hematol Oncol.
, vol.1
, pp. 20
-
-
Molckovsky, A.1
Siu, L.L.2
-
190
-
-
79958816470
-
The combination of RAD001 and NVPBEZ235 exerts synergistic anticancer activity against nonsmall cell lung cancer in vitro and in vivo
-
Xu CX, Li Y, Yue P, Owonikoko TK, Ramalingam SS, Khuri FR, Sun SY. The combination of RAD001 and NVPBEZ235 exerts synergistic anticancer activity against nonsmall cell lung cancer in vitro and in vivo. PLoS One. 2011; 6: e20899.
-
(2011)
PLoS One.
, vol.6
-
-
Xu, C.X.1
Li, Y.2
Yue, P.3
Owonikoko, T.K.4
Ramalingam, S.S.5
Khuri, F.R.6
Sun, S.Y.7
-
191
-
-
33646382364
-
A dual PI3 kinase/ mTOR inhibitor reveals emergent efficacy in glioma
-
Fan QW, Knight ZA, Goldenberg DD, Yu W, Mostov KE, Stokoe D, Shokat KM, Weiss WA. A dual PI3 kinase/ mTOR inhibitor reveals emergent efficacy in glioma. Cancer Cell. 2006; 9: 341-349.
-
(2006)
Cancer Cell.
, vol.9
, pp. 341-349
-
-
Fan, Q.W.1
Knight, Z.A.2
Goldenberg, D.D.3
Yu, W.4
Mostov, K.E.5
Stokoe, D.6
Shokat, K.M.7
Weiss, W.A.8
-
192
-
-
34548596728
-
A dual phosphoinositide-3-kinase a/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma
-
Fan QW, Cheng CK, Nicolaides TP, Hackett CS, Knight ZA, Shokat KM, Weiss WA. A dual phosphoinositide-3-kinase a/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma. Cancer Res. 2007; 67: 7960-7965.
-
(2007)
Cancer Res.
, vol.67
, pp. 7960-7965
-
-
Fan, Q.W.1
Cheng, C.K.2
Nicolaides, T.P.3
Hackett, C.S.4
Knight, Z.A.5
Shokat, K.M.6
Weiss, W.A.7
-
193
-
-
51049109033
-
Identification and characterization of NVPBEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
Maira SM, Stauffer F, Brueggen J, Furet P, Schnell C, Fritsc, C, Brachmann S, Chene P, De Pover A, Schoemaker K, Fabbro D, Gabriel D, Simonen M, Murphy L, Finan P, Sellers W, et al. Identification and characterization of NVPBEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity. Mol Cancer Ther. 2008; 7: 1851-1863.
-
(2008)
Mol Cancer Ther.
, vol.7
, pp. 1851-1863
-
-
Maira, S.M.1
Stauffer, F.2
Brueggen, J.3
Furet, P.4
Schnell, C.5
Fritsc, C.6
Brachmann, S.7
Chene, P.8
De Pover, A.9
Schoemaker, K.10
Fabbro, D.11
Gabriel, D.12
Simonen, M.13
Murphy, L.14
Finan, P.15
Sellers, W.16
-
194
-
-
78349273297
-
Dual inhibition of PI3K and mTORC1/2 signaling by NVP-BEZ235 as a new therapeutic strategy for acute myeloid leukemia
-
Chapuis N, Tamburini J, Green AS, Vignon C, Bardet V, Neyret A, Pannetier M, Willems L, Park S, Macone A, Maira SM, Ifrah N, Dreyfus F, Herault O, Lacombe C, Mayeux P, et al. Dual inhibition of PI3K and mTORC1/2 signaling by NVP-BEZ235 as a new therapeutic strategy for acute myeloid leukemia. Clin Cancer Res. 2010; 16: 5424-5435.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 5424-5435
-
-
Chapuis, N.1
Tamburini, J.2
Green, A.S.3
Vignon, C.4
Bardet, V.5
Neyret, A.6
Pannetier, M.7
Willems, L.8
Park, S.9
Macone, A.10
Maira, S.M.11
Ifrah, N.12
Dreyfus, F.13
Herault, O.14
Lacombe, C.15
Mayeux, P.16
-
195
-
-
65949088837
-
Dual inhibition of class IA phosphatidylionsitol 3-kinase and mTOR as a new therapeutic option for T-cell acute lymphoblastic leukemia
-
Chiarini F, Fala F, Tazzari PL, Ricci F, Astolfi A, Pession A, Pagliaro P, McCubrey JA, Martelli AM. Dual inhibition of class IA phosphatidylionsitol 3-kinase and mTOR as a new therapeutic option for T-cell acute lymphoblastic leukemia. Cancer Research. 2009; 69: 3520-3528.
-
(2009)
Cancer Research.
, vol.69
, pp. 3520-3528
-
-
Chiarini, F.1
Fala, F.2
Tazzari, P.L.3
Ricci, F.4
Astolfi, A.5
Pession, A.6
Pagliaro, P.7
Mccubrey, J.A.8
Martelli, A.M.9
-
196
-
-
78049241020
-
Activity of the novel dual phosphatidylinositol 3-kinasse/mammalian target of rapamycin inhibitor NVP-BEZ235 against T-cell acute lymphoblastic leukemia
-
Chiarini F, Grimaldi C, Ricci F, Tazzari PL, Evangelisti C, Ognibene A, Battistelli M, Falcieri E, Melchionda F, Pession A, Pagliaro P, McCubrey JA, Martelli AM. Activity of the novel dual phosphatidylinositol 3-kinasse/mammalian target of rapamycin inhibitor NVP-BEZ235 against T-cell acute lymphoblastic leukemia. Cancer Research. 2010; 70: 8097-8107.
-
(2010)
Cancer Research.
, vol.70
, pp. 8097-8107
-
-
Chiarini, F.1
Grimaldi, C.2
Ricci, F.3
Tazzari, P.L.4
Evangelisti, C.5
Ognibene, A.6
Battistelli, M.7
Falcieri, E.8
Melchionda, F.9
Pession, A.10
Pagliaro, P.11
McCubrey, J.A.12
Martelli, A.M.13
-
197
-
-
84864052108
-
Selective targeting of the mTORC1/2 protein kinase complexes leads to antileukemic effects in vitro and in vivo
-
Schuster K, Zheng J, Arbini AA, Zhang CC, Scaglioni PP. Selective targeting of the mTORC1/2 protein kinase complexes leads to antileukemic effects in vitro and in vivo. Blood Cancer J. 2011; 1: e34.
-
(2011)
Blood Cancer J.
, vol.1
-
-
Schuster, K.1
Zheng, J.2
Arbini, A.A.3
Zhang, C.C.4
Scaglioni, P.P.5
-
198
-
-
51349164790
-
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
-
Carracedo A, Ma L, Teruya-Feldstein J, Rojo F, Salmena L, Alimonti A, Egia A, Sasaki A. T, Thomas G, Kozma SC, Papa A, Nardella C, Cantley LC, Baselga J, Pandolfi PP. Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer. J Clin Invest. 2008; 118: 3065-3674.
-
(2008)
J Clin Invest.
, vol.118
, pp. 3065-3674
-
-
Carracedo, A.1
Ma, L.2
Teruya-Feldstein, J.3
Rojo, F.4
Salmena, L.5
Alimonti, A.6
Egia, A.7
Sasaki, A.T.8
Thomas, G.9
Kozma, S.C.10
Papa, A.11
Nardella, C.12
Cantley, L.C.13
Baselga, J.14
Pandolfi, P.P.15
-
199
-
-
79959327886
-
Progress in the preclinical discovery and clinical development of class I and dual class I/IV phosphoinositide 3-kinase (PI3K) inhibitors
-
Shuttleworth SJ, Silva FA, Cecil AR, Tomassi CD, Hill TJ, Raynaud FI, Clarke PA, Workman P. Progress in the preclinical discovery and clinical development of class I and dual class I/IV phosphoinositide 3-kinase (PI3K) inhibitors. Curr Med Chem. 2011; 18: 2686-2714.
-
(2011)
Curr Med Chem.
, vol.18
, pp. 2686-2714
-
-
Shuttleworth, S.J.1
Silva, F.A.2
Cecil, A.R.3
Tomassi, C.D.4
Hill, T.J.5
Raynaud, F.I.6
Clarke, P.A.7
Workman, P.8
-
200
-
-
79955996030
-
Antitumor efficacy of PKI-587, a highly potent dual PI3K/mTOR kinase inhibitor
-
Mallon R, Feldberg LR, Lucas J, Chaudhary I, Dehnhardt C, Santos ED, Chen Z, dos Santos O, Ayral-Kaloustian S, Venkatesan A, Hollander I. Antitumor efficacy of PKI-587, a highly potent dual PI3K/mTOR kinase inhibitor. Clin Cancer Res. 2011; 17: 3193-3203.
-
(2011)
Clin Cancer Res.
, vol.17
, pp. 3193-3203
-
-
Mallon, R.1
Feldberg, L.R.2
Lucas, J.3
Chaudhary, I.4
Dehnhardt, C.5
Santos, E.D.6
Chen, Z.7
dos Santos, O.8
Ayral-Kaloustian, S.9
Venkatesan, A.10
Hollander, I.11
-
201
-
-
84863985238
-
PKI-587 and Sorafenib Targeting PI3K/AKT/mTOR and Ras/Raf/MAPK pathways synergistically inhibit HCC cell proliferation
-
Gedaly R, Angulo P, Hundley J, Daily MF, Chen C, Evers BM. PKI-587 and Sorafenib Targeting PI3K/AKT/mTOR and Ras/Raf/MAPK pathways synergistically inhibit HCC cell proliferation. J Surg Res. 2011; 176: 542-548.
-
(2011)
J Surg Res.
, vol.176
, pp. 542-548
-
-
Gedaly, R.1
Angulo, P.2
Hundley, J.3
Daily, M.F.4
Chen, C.5
Evers, B.M.6
-
202
-
-
81055149891
-
PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity
-
Yuan J, Mehta PP, Yin MJ, Sun S, Zou A, Chen J, Rafidi K, Feng Z, Nickel J, Engebretsen J, Hallin, J, Blasina A, Zhang E, Nguyen L, Sun M, Vogt PK, et al. PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity. Mol Cancer Ther. 2011; 10: 2189-2199.
-
(2011)
Mol Cancer Ther.
, vol.10
, pp. 2189-2199
-
-
Yuan, J.1
Mehta, P.P.2
Yin, M.J.3
Sun, S.4
Zou, A.5
Chen, J.6
Rafidi, K.7
Feng, Z.8
Nickel, J.9
Engebretsen, J.10
Hallin, J.11
Blasina, A.12
Zhang, E.13
Nguyen, L.14
Sun, M.15
Vogt, P.K.16
-
203
-
-
77950810322
-
Antitumor efficacy profile of PKI-402, a dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor
-
Mallon R, Hollander I, Feldberg L, Lucas J, Soloveva V, Venkatesan A, Dehnhardt C, Delos Santos E, Chen Z, Dos Santos O, Ayral-Kaloustian S, Gibbons, J. Antitumor efficacy profile of PKI-402, a dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor. Mol Cancer Ther. 2010; 9: 976-984.
-
(2010)
Mol Cancer Ther.
, vol.9
, pp. 976-984
-
-
Mallon, R.1
Hollander, I.2
Feldberg, L.3
Lucas, J.4
Soloveva, V.5
Venkatesan, A.6
Dehnhardt, C.7
Delos Santos, E.8
Chen, Z.9
Dos Santos, O.10
Ayral-Kaloustian, S.11
Gibbons, J.12
-
204
-
-
79953052206
-
Inhibition of PI3K/mTOR pathways in glioblastoma and implications for combination therapy with temozolomide
-
Prasad G, Sottero T, Yang X, Mueller S, James CD, Weiss WA, Polley MY, Ozawa T, Berger MS, Aftab DT, Prados MD, Haas-Kogan DA. Inhibition of PI3K/mTOR pathways in glioblastoma and implications for combination therapy with temozolomide. Neuro Oncol. 2011; 13: 384-392.
-
(2011)
Neuro Oncol.
, vol.13
, pp. 384-392
-
-
Prasad, G.1
Sottero, T.2
Yang, X.3
Mueller, S.4
James, C.D.5
Weiss, W.A.6
Polley, M.Y.7
Ozawa, T.8
Berger, M.S.9
Aftab, D.T.10
Prados, M.D.11
Haas-Kogan, D.A.12
-
205
-
-
80052455843
-
Autophagy suppression promotes apoptotic cell death in response to inhibition of the PI3KmTOR pathway in pancreatic adenocarcinoma
-
Mirzoeva OK, Hann B, Hom YK, Debnath J, Aftab D, Shokat K, Korn WM. Autophagy suppression promotes apoptotic cell death in response to inhibition of the PI3KmTOR pathway in pancreatic adenocarcinoma. J Mol Med (Berl). 2011; 89: 877-889.
-
(2011)
J Mol Med (Berl).
, vol.89
, pp. 877-889
-
-
Mirzoeva, O.K.1
Hann, B.2
Hom, Y.K.3
Debnath, J.4
Aftab, D.5
Shokat, K.6
Korn, W.M.7
-
206
-
-
83355163329
-
GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway
-
Wallin JJ, Edgar KA, Guan J, Berry M, Prior WW, Lee L, Lesnick JD, Lewis C, Nonomiya J, Pang J, Salphati L, Olivero AG, Sutherlin DP, O'Brien C, Spoerke JM, Patel S, et al. GDC-0980 is a novel class I PI3K/mTOR kinase inhibitor with robust activity in cancer models driven by the PI3K pathway. Mol Cancer Ther. 2011; 10: 2426-36.
-
(2011)
Mol Cancer Ther.
, vol.10
, pp. 2426-2436
-
-
Wallin, J.J.1
Edgar, K.A.2
Guan, J.3
Berry, M.4
Prior, W.W.5
Lee, L.6
Lesnick, J.D.7
Lewis, C.8
Nonomiya, J.9
Pang, J.10
Salphati, L.11
Olivero, A.G.12
Sutherlin, D.P.13
O'Brien, C.14
Spoerke, J.M.15
Patel, S.16
-
207
-
-
77956255150
-
WJD008, a dual phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin inhibitor, prevents PI3K signaling and inhibits the proliferation of transformed cells with oncogenic PI3K mutant
-
Li T, Wang J, Wang X, Yang N, Chen SM, Tong LJ, Yang CH, Meng LH, Ding J. WJD008, a dual phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin inhibitor, prevents PI3K signaling and inhibits the proliferation of transformed cells with oncogenic PI3K mutant. J Pharmacol Exp Ther. 2010; 334: 830-838.
-
(2010)
J Pharmacol Exp Ther.
, vol.334
, pp. 830-838
-
-
Li, T.1
Wang, J.2
Wang, X.3
Yang, N.4
Chen, S.M.5
Tong, L.J.6
Yang, C.H.7
Meng, L.H.8
Ding, J.9
-
208
-
-
80053070033
-
PI3Ktargeted therapy can be evaded by gene amplification along the MYC-eukaryotic translation initiation factor 4E (eIF4E) axis
-
Ilic N, Utermark T, Widlund HR, Roberts TM. PI3Ktargeted therapy can be evaded by gene amplification along the MYC-eukaryotic translation initiation factor 4E (eIF4E) axis. Proc Natl Acad Sci USA. 2011; 108: E699-708.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
-
-
Ilic, N.1
Utermark, T.2
Widlund, H.R.3
Roberts, T.M.4
-
209
-
-
80054863376
-
A chemical-genetic screen reveals a mechanism of resistance to PI3K inhibitors in cancer
-
Muellner MK, Uras IZ, Gapp BV, Kerzendorfer C, Smida M, Lechtermann H, Craig-Mueller N, Colinge J, Duernberger G, Nijman SM. A chemical-genetic screen reveals a mechanism of resistance to PI3K inhibitors in cancer. Nat Chem Biol. 2011; 7: 787-793.
-
(2011)
Nat Chem Biol.
, vol.7
, pp. 787-793
-
-
Muellner, M.K.1
Uras, I.Z.2
Gapp, B.V.3
Kerzendorfer, C.4
Smida, M.5
Lechtermann, H.6
Craig-Mueller, N.7
Colinge, J.8
Duernberger, G.9
Nijman, S.M.10
-
210
-
-
57349154375
-
Sensitivity to the non-COX inhibiting celecoxib derivative, OSU03012, is p21(WAF1/CIP1) dependent
-
Ding H, Han C, Guo D, Wang D, Duan W, Chen CS, D'Ambrosio SM. Sensitivity to the non-COX inhibiting celecoxib derivative, OSU03012, is p21(WAF1/CIP1) dependent. Int J Cancer. 2008; 123: 2931-2938.
-
(2008)
Int J Cancer.
, vol.123
, pp. 2931-2938
-
-
Ding, H.1
Han, C.2
Guo, D.3
Wang, D.4
Duan, W.5
Chen, C.S.6
D'Ambrosio, S.M.7
-
211
-
-
65849446043
-
Growth inhibitory and anti-tumour activities of OSU-03012, a novel PDK-1 inhibitor, on vestibular schwannoma and malignant schwannoma cells
-
Lee TX, Packer MD, Huang J, Akhmametyeva EM, Kulp SK, Chen CS, Giovannini M, Jacob A, Welling DB, Chang LS. Growth inhibitory and anti-tumour activities of OSU-03012, a novel PDK-1 inhibitor, on vestibular schwannoma and malignant schwannoma cells. Eur J Cancer. 2009; 45: 1709-1720.
-
(2009)
Eur J Cancer.
, vol.45
, pp. 1709-1720
-
-
Lee, T.X.1
Packer, M.D.2
Huang, J.3
Akhmametyeva, E.M.4
Kulp, S.K.5
Chen, C.S.6
Giovannini, M.7
Jacob, A.8
Welling, D.B.9
Chang, L.S.10
-
212
-
-
74249085433
-
A novel inhibitor of the PI3K/Akt pathway based on the structure of inositol 1,3,4,5,6-pentakisphosphate
-
Falasca M, Chiozzotto D, Godage HY, Mazzoletti M, Riley AM, Previdi S, Potter BV, Broggini M, Maffucci T. A novel inhibitor of the PI3K/Akt pathway based on the structure of inositol 1,3,4,5,6-pentakisphosphate. Br J Cancer. 2010; 102: 104-114.
-
(2010)
Br J Cancer.
, vol.102
, pp. 104-114
-
-
Falasca, M.1
Chiozzotto, D.2
Godage, H.Y.3
Mazzoletti, M.4
Riley, A.M.5
Previdi, S.6
Potter, B.V.7
Broggini, M.8
Maffucci, T.9
-
213
-
-
3042743988
-
Akt/protein kinase B signaling inhibitor-2, a selective small molecule inhibitor of Akt signaling with antitumor activity in cancer cells overexpressing Akt
-
Yang L, Dan HC, Sun M, Liu Q, Sun XM, Feldman RI, Hamilton AD, Polokoff M, Nicosia SV, Herlyn M, Sebti SM, Cheng JQ. Akt/protein kinase B signaling inhibitor-2, a selective small molecule inhibitor of Akt signaling with antitumor activity in cancer cells overexpressing Akt. Cancer Res. 2004; 64: 4394-4399.
-
(2004)
Cancer Res.
, vol.64
, pp. 4394-4399
-
-
Yang, L.1
Dan, H.C.2
Sun, M.3
Liu, Q.4
Sun, X.M.5
Feldman, R.I.6
Hamilton, A.D.7
Polokoff, M.8
Nicosia, S.V.9
Herlyn, M.10
Sebti, S.M.11
Cheng, J.Q.12
-
214
-
-
80054809459
-
Phase I pharmacokinetic and pharmacodynamic study of triciribine phosphate monodrate, a small-molecule inhibitor of AKT phosphorylation, in adult subjects with solid tumors containing activated AKT
-
Garrett CR, Coppola D, Wenham RM, Cubitt CL, Neuger AM, Frost TJ, Lush RM, Sullivan DM, Cheng JQ, Sebti SM. Phase I pharmacokinetic and pharmacodynamic study of triciribine phosphate monodrate, a small-molecule inhibitor of AKT phosphorylation, in adult subjects with solid tumors containing activated AKT. Invest New Drugs. 2010; 29: 1381-1389.
-
(2010)
Invest New Drugs.
, vol.29
, pp. 1381-1389
-
-
Garrett, C.R.1
Coppola, D.2
Wenham, R.M.3
Cubitt, C.L.4
Neuger, A.M.5
Frost, T.J.6
Lush, R.M.7
Sullivan, D.M.8
Cheng, J.Q.9
Sebti, S.M.10
-
215
-
-
79953186071
-
Next-generation Akt inhibitors provide greater specificity: effects on glucose metabolism in adipocytes
-
Tan S, Ng Y, James DE. Next-generation Akt inhibitors provide greater specificity: effects on glucose metabolism in adipocytes. Biochem J. 2011; 435: 539-544.
-
(2011)
Biochem J.
, vol.435
, pp. 539-544
-
-
Tan, S.1
Ng, Y.2
James, D.E.3
-
216
-
-
84869086211
-
Cytotoxic activity of the novel Akt inhibitor, MK-2206, in T-cell acute lymphoblastic leukemia
-
In Press
-
Simioni C, Neri LM, Tabellini G, Ricci F, Bressanin D, Chiarini F, Evangelisti C, Cani A, Tazzari PL, Melchionda F, Pagliaro P, Pession A, McCubrey JA, Capitani S, Martelli AM. Cytotoxic activity of the novel Akt inhibitor, MK-2206, in T-cell acute lymphoblastic leukemia. Leukemia. 2012; In Press.
-
(2012)
Leukemia.
-
-
Simioni, C.1
Neri, L.M.2
Tabellini, G.3
Ricci, F.4
Bressanin, D.5
Chiarini, F.6
Evangelisti, C.7
Cani, A.8
Tazzari, P.L.9
Melchionda, F.10
Pagliaro, P.11
Pession, A.12
Mccubrey, J.A.13
Capitani, S.14
Martelli, A.M.15
-
217
-
-
42049115641
-
Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity
-
Rhodes N, Heerding DA, Duckett DR, Eberwein DJ, Knick VB, Lansing TJ, McConnell RT, Gilmer TM, Zhang SY, Robell K, Kahana JA, Geske RS, Kleymenova EV, Choudhry AE, Lai Z, Leber JD, et al. Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity. Cancer Res. 2008; 68: 2366-2374.
-
(2008)
Cancer Res.
, vol.68
, pp. 2366-2374
-
-
Rhodes, N.1
Heerding, D.A.2
Duckett, D.R.3
Eberwein, D.J.4
Knick, V.B.5
Lansing, T.J.6
McConnell, R.T.7
Gilmer, T.M.8
Zhang, S.Y.9
Robell, K.10
Kahana, J.A.11
Geske, R.S.12
Kleymenova, E.V.13
Choudhry, A.E.14
Lai, Z.15
Leber, J.D.16
-
218
-
-
33645728920
-
Simultaneous inhibition of PDK1/AKT and Fms-like tyrosine kinase 3 signaling by a small-molecule KP372-1 induces mitochondrial dysfunction and apoptosis in acute myelogenous leukemia
-
Zeng Z, Samudio IJ, Zhang W, Estrov Z, Pelicano H, Harris D, Frolova O, Hail N Jr, Chen W, Kornblau SM, Huang P, Lu Y, Mills GB, Andreeff M, Konopleva M. Simultaneous inhibition of PDK1/AKT and Fms-like tyrosine kinase 3 signaling by a small-molecule KP372-1 induces mitochondrial dysfunction and apoptosis in acute myelogenous leukemia. Cancer Res. 2006; 66: 3737-3746.
-
(2006)
Cancer Res.
, vol.66
, pp. 3737-3746
-
-
Zeng, Z.1
Samudio, I.J.2
Zhang, W.3
Estrov, Z.4
Pelicano, H.5
Harris, D.6
Frolova, O.7
Hail Jr., N.8
Chen, W.9
Kornblau, S.M.10
Huang, P.11
Lu, Y.12
Mills, G.B.13
Andreeff, M.14
Konopleva, M.15
-
219
-
-
84859544365
-
A phase I study of LY317615 (enzastaurin) and temozolomide in patients with gliomas (EORTC trial 26054)
-
Rampling R, Sanson M, Gorlia T, Lacombe D, Lai C, Gharib M, Taal W, Stoffregen C, Decker R, van den Bent MJ. A phase I study of LY317615 (enzastaurin) and temozolomide in patients with gliomas (EORTC trial 26054). Neuro Oncol. 2012; 14: 344-350.
-
(2012)
Neuro Oncol.
, vol.14
, pp. 344-350
-
-
Rampling, R.1
Sanson, M.2
Gorlia, T.3
Lacombe, D.4
Lai, C.5
Gharib, M.6
Taal, W.7
Stoffregen, C.8
Decker, R.9
van den Bent, M.J.10
-
220
-
-
84856040615
-
A phase II randomized study of cisplatin-pemetrexed plus either enzastaurin or placebo in chemonaive patients with advanced non-small cell lung cancer
-
Vansteenkiste J, Ramlau R, von Pawel J, San Antonio B, Eschbach C, Szczesna A, Kennedy L, Visseren-Grul C, Chouaki N, Reck M. A phase II randomized study of cisplatin-pemetrexed plus either enzastaurin or placebo in chemonaive patients with advanced non-small cell lung cancer. Oncology. 2012; 82: 25-29.
-
(2012)
Oncology.
, vol.82
, pp. 25-29
-
-
Vansteenkiste, J.1
Ramlau, R.2
von Pawel, J.3
Antonio, B.S.4
Eschbach, C.5
Szczesna, A.6
Kennedy, L.7
Visseren-Grul, C.8
Chouaki, N.9
Reck, M.10
-
221
-
-
84862691752
-
A double-blind, randomized, placebo-controlled, phase 2 study of maintenance enzastaurin with 5-fluorouracil/leucovorin plus bevacizumab after first-line therapy for metastatic colorectal cancer
-
Wolff RA, Fuchs M, Di Bartolomeo M, Hossain AM, Stoffregen C, Nicol S, Heinemann V. A double-blind, randomized, placebo-controlled, phase 2 study of maintenance enzastaurin with 5-fluorouracil/leucovorin plus bevacizumab after first-line therapy for metastatic colorectal cancer. Cancer. 2012; 118: 4132-4138.
-
(2012)
Cancer.
, vol.118
, pp. 4132-4138
-
-
Wolff, R.A.1
Fuchs, M.2
Di Bartolomeo, M.3
Hossain, A.M.4
Stoffregen, C.5
Nicol, S.6
Heinemann, V.7
-
222
-
-
2542547908
-
Perifosine, a novel alkylphospholipid, inhibits protein kinase B activation
-
Kondapaka SB, Singh SS, Dasmahapatra GP, Sausville EA, Roy KK. Perifosine, a novel alkylphospholipid, inhibits protein kinase B activation. Mol Cancer Ther. 2003; 2: 1093-1103.
-
(2003)
Mol Cancer Ther.
, vol.2
, pp. 1093-1103
-
-
Kondapaka, S.B.1
Singh, S.S.2
Dasmahapatra, G.P.3
Sausville, E.A.4
Roy, K.K.5
-
223
-
-
45149121372
-
The novel Akt inhibitor perifosine induces caspase-dependent apoptosis and downregulates P-glycoprotein expression in multidrug-resistant T-acute leukemia cells by a JNK-dependent mechanism
-
Chiarini F, Del Sole M, Mongiorgi S, Gaboardi GC, Cappellini A, Mantovani I, Follo MY, McCubrey JA, Martelli AM. The novel Akt inhibitor perifosine induces caspase-dependent apoptosis and downregulates P-glycoprotein expression in multidrug-resistant T-acute leukemia cells by a JNK-dependent mechanism. Leukemia. 2008; 22: 1106-1116.
-
(2008)
Leukemia.
, vol.22
, pp. 1106-1116
-
-
Chiarini, F.1
Del Sole, M.2
Mongiorgi, S.3
Gaboardi, G.C.4
Cappellini, A.5
Mantovani, I.6
Follo, M.Y.7
McCubrey, J.A.8
Martelli, A.M.9
-
225
-
-
33748057166
-
Increased cytotoxicity of ionizing radiation in combination with membrane-targeted apoptosis modulators involves downregulation of protein kinase B/Akt-mediated survival-signaling
-
Handrick R, Rübel A, Faltin H, Eibl H, Belka C, Jendrossek V. Increased cytotoxicity of ionizing radiation in combination with membrane-targeted apoptosis modulators involves downregulation of protein kinase B/Akt-mediated survival-signaling. Radiother Oncol. 2006; 80: 199-206.
-
(2006)
Radiother Oncol.
, vol.80
, pp. 199-206
-
-
Handrick, R.1
Rübel, A.2
Faltin, H.3
Eibl, H.4
Belka, C.5
Jendrossek, V.6
-
226
-
-
77950937717
-
Erucylphosphohomocholine, the first intravenously applicable alkylphosphocholine, is cytotoxic to acute myelogenous leukemia cells through JNK2-and PP2-dependent mechanisms
-
Martelli AM, Papa V, Tazzari PL, Evangelesti C, Chiarini F, Grimaldi C, Ricci F, Martinelli G, Ottaviani E, Pagliaro P, Horn S, Basecke J, Linder LH, Eibl H, McCubrey JA. Erucylphosphohomocholine, the first intravenously applicable alkylphosphocholine, is cytotoxic to acute myelogenous leukemia cells through JNK2-and PP2-dependent mechanisms. Leukemia. 2010; 24: 687-698.
-
(2010)
Leukemia.
, vol.24
, pp. 687-698
-
-
Martelli, A.M.1
Papa, V.2
Tazzari, P.L.3
Evangelesti, C.4
Chiarini, F.5
Grimaldi, C.6
Ricci, F.7
Martinelli, G.8
Ottaviani, E.9
Pagliaro, P.10
Horn, S.11
Basecke, J.12
Linder, L.H.13
Eibl, H.14
Mccubrey, J.A.15
-
227
-
-
77958502138
-
A first-in-human phase I trial of PBI-05204 (oleandrin), an inhibitor of Akt, FGF-2, NF-Kb, and p70S6K in advanced solid tumor patients
-
Post-Meeting Edition
-
Bidyasar S, Kurzrock R, Falchook GS, Naing A, Wheler JJ, Durand J, Yang P, Johansen MJ, Newman RA, Khan R, Hong D. A first-in-human phase I trial of PBI-05204 (oleandrin), an inhibitor of Akt, FGF-2, NF-Kb, and p70S6K in advanced solid tumor patients. Journal of Clinical Oncology, ASCO Annual Meeting Proceedings (Post-Meeting Edition). 2009; 27: 15S.
-
(2009)
Journal of Clinical Oncology, ASCO Annual Meeting Proceedings
, vol.27
-
-
Bidyasar, S.1
Kurzrock, R.2
Falchook, G.S.3
Naing, A.4
Wheler, J.J.5
Durand, J.6
Yang, P.7
Johansen, M.J.8
Newman, R.A.9
Khan, R.10
Hong, D.11
-
228
-
-
80054798016
-
In vitro and in vivo neuroprotective activity of the cardiac glycoside oleandrin from Nerium oleander in brain slice-based stroke models
-
Dunn DE, He DN, Yang P, Johansen M, Newman RA, Lo DC. In vitro and in vivo neuroprotective activity of the cardiac glycoside oleandrin from Nerium oleander in brain slice-based stroke models. J Neurochem. 2011; 119: 800-814.
-
(2011)
J Neurochem.
, vol.119
, pp. 800-814
-
-
Dunn, D.E.1
He, D.N.2
Yang, P.3
Johansen, M.4
Newman, R.A.5
Lo, D.C.6
-
229
-
-
70350435062
-
Antitumor activity of a novel antisense oligonucleotide against Akt1
-
Yoon H, Kim DJ, Ahn EH, Gellert GC, Shay JW, Ahn CH, Lee YB. Antitumor activity of a novel antisense oligonucleotide against Akt1. J Cell Biochem. 2009; 108: 832-838.
-
(2009)
J Cell Biochem.
, vol.108
, pp. 832-838
-
-
Yoon, H.1
Kim, D.J.2
Ahn, E.H.3
Gellert, G.C.4
Shay, J.W.5
Ahn, C.H.6
Lee, Y.B.7
-
230
-
-
36849041365
-
A phase I trial of RX-0201 (AKT anti-sense) in patients with an advanced cancer
-
Marshall J, Posey J, Hwang J, Malik S, Shen R, Kazempour K, White LR, Fraser KM, Chang CG, Ahn CH. A phase I trial of RX-0201 (AKT anti-sense) in patients with an advanced cancer. Journal of Clinical Oncology, ASCO Annual Meeting Proceedings Part I. 2007; 25: 18S.
-
(2007)
Journal of Clinical Oncology, ASCO Annual Meeting Proceedings Part I.
, vol.25
-
-
Marshall, J.1
Posey, J.2
Hwang, J.3
Malik, S.4
Shen, R.5
Kazempour, K.6
White, L.R.7
Fraser, K.M.8
Chang, C.G.9
Ahn, C.H.10
-
231
-
-
1942487890
-
Dissociation of raptor from mTOR is a mechanism of rapamycin-induced inhibition of mTOR function
-
Oshiro N, Yoshino K, Hidayat S, Tokunaga C, Hara K, Eguchi S, Avruch J, Yonezawa K. Dissociation of raptor from mTOR is a mechanism of rapamycin-induced inhibition of mTOR function. Genes Cells. 2004; 9: 359-366.
-
(2004)
Genes Cells.
, vol.9
, pp. 359-366
-
-
Oshiro, N.1
Yoshino, K.2
Hidayat, S.3
Tokunaga, C.4
Hara, K.5
Eguchi, S.6
Avruch, J.7
Yonezawa, K.8
-
232
-
-
36049043184
-
Rheb activates mTOR by antagonizing its endogenous inhibitor, FKBP38
-
Bai X, Ma D, Liu A, Shen X, Wang QJ, Liu Y, Jiang Y. Rheb activates mTOR by antagonizing its endogenous inhibitor, FKBP38. Science. 2007; 318: 977-980.
-
(2007)
Science.
, vol.318
, pp. 977-980
-
-
Bai, X.1
Ma, D.2
Liu, A.3
Shen, X.4
Wang, Q.J.5
Liu, Y.6
Jiang, Y.7
-
233
-
-
36049023679
-
Phase I study of Everolimus in pediatric patients with refractory solid tumors
-
Fouladi M, Laningham F, Wu J, O'Shaughnessy MA, Molina K, Broniscer A, Spunt SL, Luckett I, Stewart CF, Houghton PJ, Gilbertson RJ, Furman WL. Phase I study of Everolimus in pediatric patients with refractory solid tumors. JCO. 2007; 25: 4806-4812.
-
(2007)
JCO.
, vol.25
, pp. 4806-4812
-
-
Fouladi, M.1
Laningham, F.2
Wu, J.3
O'Shaughnessy, M.A.4
Molina, K.5
Broniscer, A.6
Spunt, S.L.7
Luckett, I.8
Stewart, C.F.9
Houghton, P.J.10
Gilbertson, R.J.11
Furman, W.L.12
-
234
-
-
80051606004
-
Potential of mTOR inhibitors for the treatment of subependymal giant cell astrocytomas in tuberous sclerosis complex
-
Major P. Potential of mTOR inhibitors for the treatment of subependymal giant cell astrocytomas in tuberous sclerosis complex. Aging. 2011; 3: 189-191.
-
(2011)
Aging.
, vol.3
, pp. 189-191
-
-
Major, P.1
-
235
-
-
79960464440
-
Exploring long-term protection of normal human fibroblasts and epithelial cells from chemotherapy in cell culture
-
Apontes P, Leontieva OV, Demidenko ZN, Li F, Blagosklonny MV. Exploring long-term protection of normal human fibroblasts and epithelial cells from chemotherapy in cell culture. Oncotarget. 2011; 2(3): 222-233.
-
(2011)
Oncotarget.
, vol.2
, Issue.3
, pp. 222-233
-
-
Apontes, P.1
Leontieva, O.V.2
Demidenko, Z.N.3
Li, F.4
Blagosklonny, M.V.5
-
236
-
-
84859489680
-
Molecular damage in cancer: an argument for mTOR-driven aging
-
Blagosklonny MV. Molecular damage in cancer: an argument for mTOR-driven aging. Aging. 2011; 3: 1130-1141.
-
(2011)
Aging.
, vol.3
, pp. 1130-1141
-
-
Blagosklonny, M.V.1
-
237
-
-
83755186554
-
Yeast-like chronological senescence in mammalian cells: phenomenon, mechanism and pharmacological suppression
-
Leontieva OV, Blagosklonny MV. Yeast-like chronological senescence in mammalian cells: phenomenon, mechanism and pharmacological suppression. Aging. 2011; 3:1078-1091.
-
(2011)
Aging.
, vol.3
, pp. 078-1091
-
-
Leontieva, O.V.1
Blagosklonny, M.V.2
-
238
-
-
79959539851
-
Normalizing a hyperactive mTOR initiates muscle growth during obesity
-
Williamson DL. Normalizing a hyperactive mTOR initiates muscle growth during obesity. Aging. 2011; 3: 83-84.
-
(2011)
Aging.
, vol.3
, pp. 83-84
-
-
Williamson, D.L.1
-
239
-
-
80055108638
-
mTOR in podocyte function: is rapamycin good for diabetic nephropathy?
-
Lu MK. Gong XG. Guan KL. mTOR in podocyte function: is rapamycin good for diabetic nephropathy?. Cell Cycle. 2011; 10: 3415-3416.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3415-3416
-
-
Lu, M.K.1
Gong, X.G.2
Guan, K.L.3
-
242
-
-
84855556875
-
Phase II study of the mammalian target of rapamycin inhibitor ridaforolimus in patients with advanced bone and soft tissue sarcomas
-
Chawla SP, Staddon AP, Baker LH, Schuetze SM, Tolcher AW, D'Amato GZ, Blay JY, Mita MM, Sankhala KK, Berk L, Rivera VM, Clackson T, Loewy JW, Haluska FG, Demetri GD. Phase II study of the mammalian target of rapamycin inhibitor ridaforolimus in patients with advanced bone and soft tissue sarcomas. J Clin Oncol. 2012; 30: 78-84.
-
(2012)
J Clin Oncol.
, vol.30
, pp. 78-84
-
-
Chawla, S.P.1
Staddon, A.P.2
Baker, L.H.3
Schuetze, S.M.4
Tolcher, A.W.5
D'Amato, G.Z.6
Blay, J.Y.7
Mita, M.M.8
Sankhala, K.K.9
Berk, L.10
Rivera, V.M.11
Clackson, T.12
Loewy, J.W.13
Haluska, F.G.14
Demetri, G.D.15
-
244
-
-
80051665056
-
mTOR as a multifunctional therapeutic target in HIV infection
-
Nicoletti F, Fagone P, Meroni P, McCubrey J, Bendtzen K. mTOR as a multifunctional therapeutic target in HIV infection. Drug Discov Today. 2011; 16:.715-721.
-
(2011)
Drug Discov Today.
, vol.16
, pp. 715-721
-
-
Nicoletti, F.1
Fagone, P.2
Meroni, P.3
Mccubrey, J.4
Bendtzen, K.5
-
245
-
-
79957530990
-
Mechanisms of mTOR inhibitor resistance in cancer therapy
-
Carew JS, Kelly KR, Nawrocki ST. Mechanisms of mTOR inhibitor resistance in cancer therapy. Target Oncol. 2011; 6: 17-27.
-
(2011)
Target Oncol.
, vol.6
, pp. 17-27
-
-
Carew, J.S.1
Kelly, K.R.2
Nawrocki, S.T.3
-
246
-
-
0033776536
-
Ubiquitination of hypoxiainducible factor requires direct binding to the betadomain of the von Hippel-Lindau protein
-
Ohh M, Park CW, Ivan M, Hoffman MA, Kim TY, Huang LE, Pavletich N, Chau V, KaelinWG. Ubiquitination of hypoxiainducible factor requires direct binding to the betadomain of the von Hippel-Lindau protein. Nat Cell Biol. 2000; 2: 423-427.
-
(2000)
Nat Cell Biol.
, vol.2
, pp. 423-427
-
-
Ohh, M.1
Park, C.W.2
Ivan, M.3
Hoffman, M.A.4
Kim, T.Y.5
Huang, L.E.6
Pavletich, N.7
Chau, V.8
Kaelin, W.G.9
-
247
-
-
74949089953
-
Vorinostat enhances the activity of temsirolimus in renal cell carcinoma through suppression of survivin levels
-
Mahalingam D, Medina EC, Esquivel JA 2nd, Espitia CM, Smith S, Oberheu K, Swords R, Kelly KR, Mita MM, Mita AC, Carew JS, Giles FJ, Nawrocki ST. Vorinostat enhances the activity of temsirolimus in renal cell carcinoma through suppression of survivin levels. Clin Cancer Res. 2010; 16: 141-153.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 141-153
-
-
Mahalingam, D.1
Medina, E.C.2
Esquivel J.A3
Espitia, C.M.4
Smith, S.5
Oberheu, K.6
Swords, R.7
Kelly, K.R.8
Mita, M.M.9
Mita, A.C.10
Carew, J.S.11
Giles, F.J.12
Nawrocki, S.T.13
-
248
-
-
23944481410
-
Phase II trial of singleagent temsirolimus (CCI-779) for relapsed mantle cell lymphoma
-
Witzig TE, Geyer SM, Ghobrial I, Inwards DJ, Fonseca R, Kurtin P, Ansell SM, Luyun R, Flynn PJ, Morton RF, Dakhil SR, Gross H, Kaufmann SH. Phase II trial of singleagent temsirolimus (CCI-779) for relapsed mantle cell lymphoma. J Clin Oncol. 2005; 23: 5347-5356.
-
(2005)
J Clin Oncol.
, vol.23
, pp. 5347-5356
-
-
Witzig, T.E.1
Geyer, S.M.2
Ghobrial, I.3
Inwards, D.J.4
Fonseca, R.5
Kurtin, P.6
Ansell, S.M.7
Luyun, R.8
Flynn, P.J.9
Morton, R.F.10
Dakhil, S.R.11
Gross, H.12
Kaufmann, S.H.13
-
249
-
-
0029004755
-
Dominant mutations confer resistance to the immunosuppressant, rapamycin, in variants of a T cell lymphoma
-
Dumont FJ, Staruch MJ, Grammer T, Blenis J, Kastner CA, Rupprecht KM. Dominant mutations confer resistance to the immunosuppressant, rapamycin, in variants of a T cell lymphoma. Cell Immunol. 1995; 163: 70-79.
-
(1995)
Cell Immunol.
, vol.163
, pp. 70-79
-
-
Dumont, F.J.1
Staruch, M.J.2
Grammer, T.3
Blenis, J.4
Kastner, C.A.5
Rupprecht, K.M.6
-
250
-
-
0028923877
-
FK506 binding protein 12 mediates sensitivity to both FK506 and rapamycin in murine mast cells
-
Fruman DA, Wood MA, Gjertson CK, Katz HR, Burakoff SJ, Bierer BE. FK506 binding protein 12 mediates sensitivity to both FK506 and rapamycin in murine mast cells. Eur J Immunol. 1995; 25: 563-571.
-
(1995)
Eur J Immunol.
, vol.25
, pp. 563-571
-
-
Fruman, D.A.1
Wood, M.A.2
Gjertson, C.K.3
Katz, H.R.4
Burakoff, S.J.5
Bierer, B.E.6
-
251
-
-
0028825698
-
TOR mutations confer rapamycin resistance by preventing interaction with FKBP12-rapamycin
-
Lorenz MC, Heitman J. TOR mutations confer rapamycin resistance by preventing interaction with FKBP12-rapamycin. J Biol Chem. 1995; 270: 27531-27537.
-
(1995)
J Biol Chem.
, vol.270
, pp. 27531-27537
-
-
Lorenz, M.C.1
Heitman, J.2
-
252
-
-
13244278180
-
The Pim kinases control rapamycin-resistant T cell survival and activation
-
Fox CJ, Hammerman PS, Thompson CB. The Pim kinases control rapamycin-resistant T cell survival and activation. J Exp Med. 2005; 201: 259-266.
-
(2005)
J Exp Med.
, vol.201
, pp. 259-266
-
-
Fox, C.J.1
Hammerman, P.S.2
Thompson, C.B.3
-
253
-
-
84862986683
-
PIM kinase isoform specific regulation of MIG6 expression and EGFR signaling in prostate cancer cells
-
Siu A, Virtanen C, Jongstra J. PIM kinase isoform specific regulation of MIG6 expression and EGFR signaling in prostate cancer cells. Oncotarget. 2011; 2: 1134-1144.
-
(2011)
Oncotarget.
, vol.2
, pp. 1134-1144
-
-
Siu, A.1
Virtanen, C.2
Jongstra, J.3
-
254
-
-
80055113062
-
The direct Myc target Pim3 cooperates with other Pim kinases in supporting viability of Mycinduced B-cell lymphomas
-
Forshell LP, Li Y, Forshell TZ, Rudelius M, Nilsson L, Keller U, Nilsson J. The direct Myc target Pim3 cooperates with other Pim kinases in supporting viability of Mycinduced B-cell lymphomas. Oncotarget. 2011; 2: 448-460.
-
(2011)
Oncotarget.
, vol.2
, pp. 448-460
-
-
Forshell, L.P.1
Li, Y.2
Forshell, T.Z.3
Rudelius, M.4
Nilsson, L.5
Keller, U.6
Nilsson, J.7
-
255
-
-
19344374597
-
Pim and Akt oncogenes are independent regulators of hematopoietic cell growth and survival
-
Hammerman PS, Fox CJ, Birnbaum MJ, Thompson CB. Pim and Akt oncogenes are independent regulators of hematopoietic cell growth and survival. Blood. 2005; 105: 4477-4483.
-
(2005)
Blood.
, vol.105
, pp. 4477-4483
-
-
Hammerman, P.S.1
Fox, C.J.2
Birnbaum, M.J.3
Thompson, C.B.4
-
256
-
-
79551662915
-
The Pim protein kinases regulate energy metabolism and cell growth
-
Beharry Z, Mahajan S, Zemskova M, Lin YW, Tholanikunnel BG, Xia Z, Smith CD, Kraft AS. The Pim protein kinases regulate energy metabolism and cell growth. Proc Natl Acad Sci USA. 2011; 108: 528-533.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 528-533
-
-
Beharry, Z.1
Mahajan, S.2
Zemskova, M.3
Lin, Y.W.4
Tholanikunnel, B.G.5
Xia, Z.6
Smith, C.D.7
Kraft, A.S.8
-
257
-
-
0030609009
-
Enforced expression of the Mr 33,000 Pim-1 kinase enhances factor-independent survival and inhibits apoptosis in murine myeloid cells
-
Lilly M, Kraft A. Enforced expression of the Mr 33,000 Pim-1 kinase enhances factor-independent survival and inhibits apoptosis in murine myeloid cells. Cancer Res. 1997; 57: 5348-5355.
-
(1997)
Cancer Res.
, vol.57
, pp. 5348-5355
-
-
Lilly, M.1
Kraft, A.2
-
258
-
-
68149158207
-
PIM1 protein kinase regulates PRAS40 phosphorylation and mTOR activity in FDCP1 cells
-
Zhang F, Beharry ZM, Harris TE, Lilly MB, Smith CD, Mahajan S, Kraft AS. PIM1 protein kinase regulates PRAS40 phosphorylation and mTOR activity in FDCP1 cells. Cancer Biol Ther. 2009; 8: 846-853.
-
(2009)
Cancer Biol Ther.
, vol.8
, pp. 846-853
-
-
Zhang, F.1
Beharry, Z.M.2
Harris, T.E.3
Lilly, M.B.4
Smith, C.D.5
Mahajan, S.6
Kraft, A.S.7
-
259
-
-
78249287240
-
B55beta-associated PP2A complex controls PDK1-directed myc signaling and modulates rapamycin sensitivity in colorectal cancer
-
Tan J, Lee PL, Li Z, Jiang X, Lim YC, Hooi SC, Yu Q. B55beta-associated PP2A complex controls PDK1-directed myc signaling and modulates rapamycin sensitivity in colorectal cancer. Cancer Cell. 2010; 18: 459-471.
-
(2010)
Cancer Cell.
, vol.18
, pp. 459-471
-
-
Tan, J.1
Lee, P.L.2
Li, Z.3
Jiang, X.4
Lim, Y.C.5
Hooi, S.C.6
Yu, Q.7
-
260
-
-
0037134480
-
4E-binding proteins the suppressors of eukaryotic initiation factor 4E, are downregulated in cells with acquired or intrinsic resistance to rapamycin
-
Dilling MB, Germain GS, Dudkin L, Jayaraman AL, Zhang X, Harwood FC, Houghton PJ. 4E-binding proteins the suppressors of eukaryotic initiation factor 4E, are downregulated in cells with acquired or intrinsic resistance to rapamycin. J Biol Chem. 2002; 277: 13907-13917.
-
(2002)
J Biol Chem.
, vol.277
, pp. 13907-13917
-
-
Dilling, M.B.1
Germain, G.S.2
Dudkin, L.3
Jayaraman, A.L.4
Zhang, X.5
Harwood, F.C.6
Houghton, P.J.7
-
261
-
-
0029977949
-
Rapamycin resistance tied to defective regulation of p27Kip1
-
Luo Y, Marx SO, Kiyokawa H, Koff A, Massague J, Marks AR. Rapamycin resistance tied to defective regulation of p27Kip1. Mol Cell Biol. 1996; 16: 6744-6751.
-
(1996)
Mol Cell Biol.
, vol.16
, pp. 6744-6751
-
-
Luo, Y.1
Marx, S.O.2
Kiyokawa, H.3
Koff, A.4
Massague, J.5
Marks, A.R.6
-
262
-
-
79953668112
-
The physiology and pathophysiology of rapamycin resistance: implications for cancer
-
Gruppuso PA, Boylan JM, Sanders JA. The physiology and pathophysiology of rapamycin resistance: implications for cancer. Cell Cycle. 2011; 10: 1050-1058.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1050-1058
-
-
Gruppuso, P.A.1
Boylan, J.M.2
Sanders, J.A.3
-
263
-
-
54449091769
-
Superoxide anions regulate TORC1 and its ability to bind Fpr1: rapamycin complex
-
Neklesa TK, Davis RW. Superoxide anions regulate TORC1 and its ability to bind Fpr1: rapamycin complex. Proc Natl Acad Sci USA. 2008; 105: 15166-15171.
-
(2008)
Proc Natl Acad Sci USA.
, vol.105
, pp. 15166-15171
-
-
Neklesa, T.K.1
Davis, R.W.2
-
264
-
-
67650071137
-
Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach?
-
Trachootham D, Alexandre J, Huang P. Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach? Nat Rev Drug Discov. 2009; 8: 579-591.
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 579-591
-
-
Trachootham, D.1
Alexandre, J.2
Huang, P.3
-
265
-
-
2942724235
-
mTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathways
-
Majumder PK, Febbo PG, Bikoff R, Berger R, Xue Q, McMahon LM, Manola J, Brugarolas J, McDonnell TJ, Golub TR, Loda M, Lane HA, Sellers WR. mTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathways. Nat Med. 2004; 10: 594-601.
-
(2004)
Nat Med.
, vol.10
, pp. 594-601
-
-
Majumder, P.K.1
Febbo, P.G.2
Bikoff, R.3
Berger, R.4
Xue, Q.5
Mcmahon, L.M.6
Manola, J.7
Brugarolas, J.8
Mcdonnell, T.J.9
Golub, T.R.10
Loda, M.11
Lane, H.A.12
Sellers, W.R.13
-
266
-
-
0036174289
-
Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor
-
Guba M, von Breitenbuch P, Steinbauer M, Koehl G, Flegel S, Hornung M, Bruns CJ, Zuelke C, Farkas S, Anthuber M, Jauch KW, Geissler EK. Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med. 2002; 8: 128-135.
-
(2002)
Nat Med.
, vol.8
, pp. 128-135
-
-
Guba, M.1
von Breitenbuch, P.2
Steinbauer, M.3
Koehl, G.4
Flegel, S.5
Hornung, M.6
Bruns, C.J.7
Zuelke, C.8
Farkas, S.9
Anthuber, M.10
Jauch, K.W.11
Geissler, E.K.12
-
267
-
-
77953593619
-
Dual-targeting of mTOR and HSP90 for cancer therapy: facing oncogenic feed-back-loops and acquired mTOR resistance
-
Stoeltzing O. Dual-targeting of mTOR and HSP90 for cancer therapy: facing oncogenic feed-back-loops and acquired mTOR resistance. Cell Cycle. 2010; 9: 2051-2052.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2051-2052
-
-
Stoeltzing, O.1
-
268
-
-
80051590039
-
Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: distinct from rapamycin
-
Bhagwat SV, Gokhale PC, Crew AP, Cooke A, Yao Y, Mantis C, Kahler J, Workman J, Bittner M, Dudkin L, Epstein DM, Gibson NW, Wild R, Arnold LD, Houghton PJ, Pachter JA. Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: distinct from rapamycin. Mol Cancer Ther. 2011; 10: 1394-1406.
-
(2011)
Mol Cancer Ther.
, vol.10
, pp. 1394-1406
-
-
Bhagwat, S.V.1
Gokhale, P.C.2
Crew, A.P.3
Cooke, A.4
Yao, Y.5
Mantis, C.6
Kahler, J.7
Workman, J.8
Bittner, M.9
Dudkin, L.10
Epstein, D.M.11
Gibson, N.W.12
Wild, R.13
Arnold, L.D.14
Houghton, P.J.15
Pachter, J.A.16
-
269
-
-
84856757946
-
AMP-dependent kinase/mammalian target of rapamycin complex 1 signaling in T-cell acute lymphoblastic leukemia: therapeutic implications
-
Grimaldi C, Chiarini F, Tabellini G, Ricci F, Tazzari PL, Battistelli M, Falcieri E, Bortul R, Melchionda F, Iacobucci I, Pagliaro P, Martinelli G, Pession A, Barata JT, McCubrey JA, Martelli AM. AMP-dependent kinase/mammalian target of rapamycin complex 1 signaling in T-cell acute lymphoblastic leukemia: therapeutic implications. Leukemia. 2012; 26: 91-100.
-
(2012)
Leukemia.
, vol.26
, pp. 91-100
-
-
Grimaldi, C.1
Chiarini, F.2
Tabellini, G.3
Ricci, F.4
Tazzari, P.L.5
Battistelli, M.6
Falcieri, E.7
Bortul, R.8
Melchionda, F.9
Iacobucci, I.10
Pagliaro, P.11
Martinelli, G.12
Pession, A.13
Barata, J.T.14
Mccubrey, J.A.15
Martelli, A.M.16
-
270
-
-
77955443001
-
Critical roles for mTORC2-and rapamycininsensitive mTORC1 complexes in growth and survival of BCR ABL expressing leukemic cells
-
Carayol N, Vakana E, Sassano A, Kaur S, Goussetis DJ, Glaser H, Druker BJ, Donato NJ, Altman JK, Barr S, Platanias LC. Critical roles for mTORC2-and rapamycininsensitive mTORC1 complexes in growth and survival of BCR ABL expressing leukemic cells. Proc Natl Acad Sci USA. 2010; 107: 12469-12474.
-
(2010)
Proc Natl Acad Sci USA.
, vol.107
, pp. 12469-12474
-
-
Carayol, N.1
Vakana, E.2
Sassano, A.3
Kaur, S.4
Goussetis, D.J.5
Glaser, H.6
Druker, B.J.7
Donato, N.J.8
Altman, J.K.9
Barr, S.10
Platanias, L.C.11
-
271
-
-
79951651465
-
First-in-human phase I study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma
-
Tan DS, Dumez H, Olmos D, Sandhu SK, Hoeben A, Stephens AW, Poondru S, Gedrich R, Kaye SB, Schoffski P. First-in-human phase I study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma. J Clin Onco. 2010; 128:15s.
-
(2010)
J Clin Onco.
, vol.128
-
-
Tan, D.S.1
Dumez, H.2
Olmos, D.3
Sandhu, S.K.4
Hoeben, A.5
Stephens, A.W.6
Poondru, S.7
Gedrich, R.8
Kaye, S.B.9
Schoffski, P.10
-
272
-
-
77952931508
-
INK128 is a potent and selective TORC1/2 inhibitor with broad oral antitumor activity
-
Abstr.
-
Jessen, K, Jessen K, Wang S, Kessler L, Guo X, Kucharski J, Staunton J, Lan L, Elia M, Stewart J, Brown J, Li L, Chan K, Martin M, Ren P, Rommel C, et al. INK128 is a potent and selective TORC1/2 inhibitor with broad oral antitumor activity. Mol. Cancer Ther. 2009; 8: (Suppl. 12), Abstr. B148.
-
(2009)
Mol. Cancer Ther.
, vol.8
, Issue.SUPPL. 12
-
-
Jessen, K.1
Jessen, K.2
Wang, S.3
Kessler, L.4
Guo, X.5
Kucharski, J.6
Staunton, J.7
Lan, L.8
Elia, M.9
Stewart, J.10
Brown, J.11
Li, L.12
Chan, K.13
Martin, M.14
Ren, P.15
Rommel, C.16
-
273
-
-
77958027783
-
Targeting eukaryotic translation initiation factor 4E (eIF4E) in cancer
-
Hsieh AC, Ruggero D. Targeting eukaryotic translation initiation factor 4E (eIF4E) in cancer. Clin Cancer Res. 2010; 16: 4914-4920.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 4914-4920
-
-
Hsieh, A.C.1
Ruggero, D.2
-
274
-
-
84862777192
-
The translational landscape of mTOR signalling steers cancer initiation and metastasis
-
Hsieh AC, Liu Y, Edlind MP, Ingolia NT, Janes MR, Sher A, Shi EY, Stumpf CR, Christensen C, Bonham MJ, Wang S, Ren P, Martin M, Jessen K, Feldman ME, Weissman JS, et al. The translational landscape of mTOR signalling steers cancer initiation and metastasis. Nature. 2012; 485: 55-61.
-
(2012)
Nature.
, vol.485
, pp. 55-61
-
-
Hsieh, A.C.1
Liu, Y.2
Edlind, M.P.3
Ingolia, N.T.4
Janes, M.R.5
Sher, A.6
Shi, E.Y.7
Stumpf, C.R.8
Christensen, C.9
Bonham, M.J.10
Wang, S.11
Ren, P.12
Martin, M.13
Jessen, K.14
Feldman, M.E.15
Weissman, J.S.16
-
275
-
-
75149112670
-
AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity
-
Chresta CM, Davies BR, Hickson I, Harding T, Cosulich S, Critchlow SE, Vincent JP, Ellston R, Jones D, Sini P, James D, Howard Z, Dudley P, Hughes G, Smith L, Maguire S, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity. Cancer Res. 2010; 70: 288-298.
-
(2010)
Cancer Res.
, vol.70
, pp. 288-298
-
-
Chresta, C.M.1
Davies, B.R.2
Hickson, I.3
Harding, T.4
Cosulich, S.5
Critchlow, S.E.6
Vincent, J.P.7
Ellston, R.8
Jones, D.9
Sini, P.10
James, D.11
Howard, Z.12
Dudley, P.13
Hughes, G.14
Smith, L.15
Maguire, S.16
-
276
-
-
80054752120
-
First results from a phase I trial of AZD8055, a dual mTORC1 and mTORC2 inhibitor
-
abstr 3096
-
Banerji U, Aghajanian C, Raymond E, Kurzrock R, Blanco-Codesido M, Oelmann E, Grinsted L, Burke W, Kaye SB, Naing A. First results from a phase I trial of AZD8055, a dual mTORC1 and mTORC2 inhibitor. J Clin Oncol. 2011; 29: (suppl; abstr 3096).
-
(2011)
J Clin Oncol.
, vol.29
, Issue.SUPPL
-
-
Banerji, U.1
Aghajanian, C.2
Raymond, E.3
Kurzrock, R.4
Blanco-Codesido, M.5
Oelmann, E.6
Grinsted, L.7
Burke, W.8
Kaye, S.B.9
Naing, A.10
-
277
-
-
56449087509
-
Palomid 529, a novel small-molecule drug, is a TORC1/TORC2 inhibitor that reduces tumor growth, tumor angiogenesis, and vascular permeability
-
Xue Q, Hopkins B, Perruzzi C, Udayakumar D, Sherris D, Benjamin LE. Palomid 529, a novel small-molecule drug, is a TORC1/TORC2 inhibitor that reduces tumor growth, tumor angiogenesis, and vascular permeability. Cancer Res. 2008; 68: 9551-9557.
-
(2008)
Cancer Res.
, vol.68
, pp. 9551-9557
-
-
Xue, Q.1
Hopkins, B.2
Perruzzi, C.3
Udayakumar, D.4
Sherris, D.5
Benjamin, L.E.6
-
278
-
-
76549107351
-
Beyond rapalog therapy: preclinical pharmacology and antitumor activity of WYE 125132, an ATP-competitive and specific inhibitor of mTORC1 and mTORC2
-
Yu K, Shi C, Toral-Barza L, Lucas J, Shor B, Kim JE, Zhang WG, Mahoney R, Gaydos C, Tardio L, Kim SK, Conant R, Curran K, Kaplan J, Verheijen J, Ayral-Kaloustian S, et al. Beyond rapalog therapy: preclinical pharmacology and antitumor activity of WYE 125132, an ATP-competitive and specific inhibitor of mTORC1 and mTORC2. Cancer Res. 2010; 70: 621-631.
-
(2010)
Cancer Res.
, vol.70
, pp. 621-631
-
-
Yu, K.1
Shi, C.2
Toral-Barza, L.3
Lucas, J.4
Shor, B.5
Kim, J.E.6
Zhang, W.G.7
Mahoney, R.8
Gaydos, C.9
Tardio, L.10
Kim, S.K.11
Conant, R.12
Curran, K.13
Kaplan, J.14
Verheijen, J.15
Ayral-Kaloustian, S.16
-
279
-
-
67650312583
-
0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR)
-
Garcìa-Martìnez JM, Moran J, Clarke RG, Gray A, Cosulich SC, Chresta CM, Alessi DR Ku. 0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR). Biochem J. 2009; 421: 29-42.
-
(2009)
Biochem J.
, vol.421
, pp. 29-42
-
-
Garcìa-Martìnez, J.M.1
Moran, J.2
Clarke, R.G.3
Gray, A.4
Cosulich, S.C.5
Chresta, C.M.6
Ku, A.D.R.7
-
280
-
-
79952216582
-
Reduced VEGF production, angiogenesis, and vascular regrowth contribute to the antitumor properties of dual mTORC1/ mTORC2 inhibitors
-
Falcon BL, Barr S, Gokhale PC, Chou J, Fogarty J, Depeille P, Miglarese M, Epstein DM, McDonald DM. Reduced VEGF production, angiogenesis, and vascular regrowth contribute to the antitumor properties of dual mTORC1/ mTORC2 inhibitors. Cancer Res. 2011; 71: 1573-1583.
-
(2011)
Cancer Res.
, vol.71
, pp. 1573-1583
-
-
Falcon, B.L.1
Barr, S.2
Gokhale, P.C.3
Chou, J.4
Fogarty, J.5
Depeille, P.6
Miglarese, M.7
Epstein, D.M.8
Mcdonald, D.M.9
-
281
-
-
79952265072
-
Discovery of 9 (6 aminopyridin-3 yl)-1 (3-(trifluoromethyl)phenyl)benzo[h][1,6] naphthyridin 2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer
-
Liu Q, Wang J, Kang SA, Thoreen CC, Hur W, Ahmed T, Sabatini DM, Gray NS. Discovery of 9 (6 aminopyridin-3 yl)-1 (3-(trifluoromethyl)phenyl)benzo[h][1,6] naphthyridin 2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer. J Med Chem. 2011; 54: 1473-1480.
-
(2011)
J Med Chem.
, vol.54
, pp. 1473-1480
-
-
Liu, Q.1
Wang, J.2
Kang, S.A.3
Thoreen, C.C.4
Hur, W.5
Ahmed, T.6
Sabatini, D.M.7
Gray, N.S.8
-
282
-
-
67749111502
-
The LKB1-AMPK pathway: metabolism and growth control in tumour suppression
-
Shackelford DB, Shaw RJ. The LKB1-AMPK pathway: metabolism and growth control in tumour suppression. Nat Rev Cancer. 2009; 9: 563-575.
-
(2009)
Nat Rev Cancer.
, vol.9
, pp. 563-575
-
-
Shackelford, D.B.1
Shaw, R.J.2
-
283
-
-
42949139481
-
AMPK phosphorylation of raptor mediates a metabolic checkpoint
-
Gwinn DM, Shackelford DB, Egan DF, Mihaylova MM, Mery A, Vasquez DS, Turk BE, Shaw RJ. AMPK phosphorylation of raptor mediates a metabolic checkpoint. Mol Cell. 2008; 30: 214-226.
-
(2008)
Mol Cell.
, vol.30
, pp. 214-226
-
-
Gwinn, D.M.1
Shackelford, D.B.2
Egan, D.F.3
Mihaylova, M.M.4
Mery, A.5
Vasquez, D.S.6
Turk, B.E.7
Shaw, R.J.8
-
284
-
-
84858695046
-
Cancer Risk in Diabetic Patients Treated with Metformin: A Systematic Review and Meta-analysis
-
Noto H, Goto A, Tsujimoto T, Noda M. Cancer Risk in Diabetic Patients Treated with Metformin: A Systematic Review and Meta-analysis. PLoS One. 2012; 7: e33411.
-
(2012)
PLoS One.
, vol.7
-
-
Noto, H.1
Goto, A.2
Tsujimoto, T.3
Noda, M.4
-
285
-
-
79959564452
-
If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice
-
Albany NY
-
Anisimov VN, Berstein LM, Popovich IG, Zabezhinski MA, Egormin PA, Piskunova TS, Semenchenko AV, Tyndyk ML, Yurova MN, Kovalenko IG, Poroshina TE. If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice. Aging (Albany NY). 2011; 3: 148-157.
-
(2011)
Aging
, vol.3
, pp. 148-157
-
-
Anisimov, V.N.1
Berstein, L.M.2
Popovich, I.G.3
Zabezhinski, M.A.4
Egormin, P.A.5
Piskunova, T.S.6
Semenchenko, A.V.7
Tyndyk, M.L.8
Yurova, M.N.9
Kovalenko, I.G.10
Poroshina, T.E.11
-
286
-
-
84857975015
-
Metformin: multi-faceted protection against cancer
-
Del Barco S, Vazquez-Martin A, Cufi S, Oliveras-Ferraros C, Bosch-Barrera J, Joven J, Martin-Castillo B, Menendez JA. Metformin: multi-faceted protection against cancer. Oncotarget. 2011; 2: 896-917.
-
(2011)
Oncotarget.
, vol.2
, pp. 896-917
-
-
Del Barco, S.1
Vazquez-Martin, A.2
Cufi, S.3
Oliveras-Ferraros, C.4
Bosch-Barrera, J.5
Joven, J.6
Martin-Castillo, B.7
Menendez, J.A.8
-
287
-
-
80052401268
-
Reversing the Warburg effect through stromal autophagy
-
Richardson AD, Scott DA. Reversing the Warburg effect through stromal autophagy. Cell Cycle. 2011; 10: 2830-2831.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2830-2831
-
-
Richardson, A.D.1
Scott, D.A.2
-
288
-
-
79952666779
-
A STAT3-mediated metabolic switch is involved in tumour transformation and STAT3 addiction
-
Demaria M, Giorgi C, Lebiedzinska M, Esposito G, D'Angeli L, Bartoli A, Gough DJ, Turkson J, Levy DE, Watson CJ, Wieckowski MR, Provero P, Pinton P, Poli V. A STAT3-mediated metabolic switch is involved in tumour transformation and STAT3 addiction. Aging. 2010; 2: 823-842.
-
(2010)
Aging.
, vol.2
, pp. 823-842
-
-
Demaria, M.1
Giorgi, C.2
Lebiedzinska, M.3
Esposito, G.4
D'Angeli, L.5
Bartoli, A.6
Gough, D.J.7
Turkson, J.8
Levy, D.E.9
Watson, C.J.10
Wieckowski, M.R.11
Provero, P.12
Pinton, P.13
Poli, V.14
-
289
-
-
79952255381
-
STAT3, HIF-1, glucose addiction and Warburg effect
-
Darnell JE Jr. STAT3, HIF-1, glucose addiction and Warburg effect. Aging. 2010; 2: 890-891.
-
(2010)
Aging.
, vol.2
, pp. 890-891
-
-
Darnell Jr., J.E.1
-
290
-
-
83755186557
-
Metformin and the ATM DNA damage response (DDR): accelerating the onset of stress-induced senescence to boost protection against cancer
-
Menendez JA, Cufi S, Oliveras-Ferraros C, Martin-Castillo B, Joven J, Vellon L, Vazquez-Martin A. Metformin and the ATM DNA damage response (DDR): accelerating the onset of stress-induced senescence to boost protection against cancer. Aging. 2011; 3: 1063-1077.
-
(2011)
Aging.
, vol.3
, pp. 1063-1077
-
-
Menendez, J.A.1
Cufi, S.2
Oliveras-Ferraros, C.3
Martin-Castillo, B.4
Joven, J.5
Vellon, L.6
Vazquez-Martin, A.7
-
291
-
-
80855165212
-
Genome protective effect of metformin as revealed by reduced level of constitutive DNA damage signaling
-
Halicka HD, Zhao H, Li J, Traganos F, Zhang S, Lee M, Darzynkiewicz Z. Genome protective effect of metformin as revealed by reduced level of constitutive DNA damage signaling. Aging. 2011; 3: 1028-1038.
-
(2011)
Aging.
, vol.3
, pp. 1028-1038
-
-
Halicka, H.D.1
Zhao, H.2
Li, J.3
Traganos, F.4
Zhang, S.5
Lee, M.6
Darzynkiewicz, Z.7
-
292
-
-
84862248731
-
A phase I study of temsirolimus and metformin in advanced solid tumours
-
Mackenzie MJ, Ernst S, Johnson C, Winquist E. A phase I study of temsirolimus and metformin in advanced solid tumours. Invest New Drugs. 2010; 30: 647-652.
-
(2010)
Invest New Drugs.
, vol.30
, pp. 647-652
-
-
Mackenzie, M.J.1
Ernst, S.2
Johnson, C.3
Winquist, E.4
-
293
-
-
11244264754
-
Farnesylthiosalicylic acid inhibits mammalian target of rapamycin (mTOR) activity both in cells and in vitro by promoting dissociation of the mTOR-raptor complex
-
McMahon LP, Yue W, Santen RJ, Lawrence JC Jr. Farnesylthiosalicylic acid inhibits mammalian target of rapamycin (mTOR) activity both in cells and in vitro by promoting dissociation of the mTOR-raptor complex. Mol Endocrinol. 2005; 19: 175-183.
-
(2005)
Mol Endocrinol.
, vol.19
, pp. 175-183
-
-
McMahon, L.P.1
Yue, W.2
Santen, R.J.3
Lawrence Jr., J.C.4
-
294
-
-
26444574802
-
Development of farnesyl transferase inhibitors: a review
-
Appels NM, Beijnen JH, Schellens JH. Development of farnesyl transferase inhibitors: a review. Oncologist. 2005; 10: 565-578.
-
(2005)
Oncologist.
, vol.10
, pp. 565-578
-
-
Appels, N.M.1
Beijnen, J.H.2
Schellens, J.H.3
-
296
-
-
34648832173
-
FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia
-
Neviani P, Santhanam R, Oaks JJ, Eiring AM, Notari M, Blaser BW, Liu S, Trotta R, Muthusamy N, Gambacorti-Passerini C, Druker BJ, Cortes J, Marcucci G, Chen CS, Verrills N. M, Roy DC, et al. FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia. J Clin Invest. 2007; 117: 2408-2421.
-
(2007)
J Clin Invest.
, vol.117
, pp. 2408-2421
-
-
Neviani, P.1
Santhanam, R.2
Oaks, J.J.3
Eiring, A.M.4
Notari, M.5
Blaser, B.W.6
Liu, S.7
Trotta, R.8
Muthusamy, N.9
Gambacorti-Passerini, C.10
Druker, B.J.11
Cortes, J.12
Marcucci, G.13
Chen, C.S.14
Verrills, N.M.15
Roy, D.C.16
-
297
-
-
27744565979
-
Synergistic inhibition of human melanoma proliferation by combination treatment with B-Raf inhibitor BAY43-9006 and mTOR inhibitor rapamycin
-
Molhoek KR, Brautigan DL, Slingluff CL Jr. Synergistic inhibition of human melanoma proliferation by combination treatment with B-Raf inhibitor BAY43-9006 and mTOR inhibitor rapamycin. J Transl Med. 2003; 3: 39.
-
(2003)
J Transl Med.
, vol.3
, pp. 39
-
-
Molhoek, K.R.1
Brautigan, D.L.2
Slingluff Jr., C.L.3
-
298
-
-
57349194139
-
Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H104R murine lung cancers
-
Engleman JA, Chen L, Tan X, Crosby K, Guimaraes AR, Upadhyay R, Maira M, McNamara K, Perera SA, Song Y, Chirieac LR, Kaur R, Lightbown A, Simendinger J, Li T, Padera RF, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H104R murine lung cancers. Nat Med. 2008; 14: 1351-1356.
-
(2008)
Nat Med.
, vol.14
, pp. 1351-1356
-
-
Engleman, J.A.1
Chen, L.2
Tan, X.3
Crosby, K.4
Guimaraes, A.R.5
Upadhyay, R.6
Maira, M.7
McNamara, K.8
Perera, S.A.9
Song, Y.10
Chirieac, L.R.11
Kaur, R.12
Lightbown, A.13
Simendinger, J.14
Li, T.15
Padera, R.F.16
-
299
-
-
52649085241
-
Effects of rapamycin alone and in combination with sorafenib in an orthotopic model of human hepatocellular carcinoma
-
Wang Z, Zhou J, Fan J, Qiu SJ, Yu Y, Huang XW, Tang ZY. Effects of rapamycin alone and in combination with sorafenib in an orthotopic model of human hepatocellular carcinoma. Clin Cancer Res. 2008; 14: 5124-5130.
-
(2008)
Clin Cancer Res.
, vol.14
, pp. 5124-5130
-
-
Wang, Z.1
Zhou, J.2
Fan, J.3
Qiu, S.J.4
Yu, Y.5
Huang, X.W.6
Tang, Z.Y.7
-
300
-
-
80054118460
-
Synergistic action of a RAF inhibitor and a dual PI3K/ mTOR inhibitor in thyroid cancer
-
Jin N, Jiang T, Rosen DM, Nelkin BD, Ball DW. Synergistic action of a RAF inhibitor and a dual PI3K/ mTOR inhibitor in thyroid cancer. Clin Cancer Res. 2011; 17: 6482-6489.
-
(2011)
Clin Cancer Res.
, vol.17
, pp. 6482-6489
-
-
Jin, N.1
Jiang, T.2
Rosen, D.M.3
Nelkin, B.D.4
Ball, D.W.5
-
301
-
-
37049010979
-
Targeting protein translation in human non-small cell lung cancer via combined MEK and mammalian target of rapamycin suppression
-
Legrier ME, Yang CP, Yan HG, Lopez-Barcons L, Keller SM, Perez-Soler R, Horwitz SB, McDaid HM. Targeting protein translation in human non-small cell lung cancer via combined MEK and mammalian target of rapamycin suppression. Cancer Res. 2007; 67: 11300-11308.
-
(2007)
Cancer Res.
, vol.67
, pp. 11300-11308
-
-
Legrier, M.E.1
Yang, C.P.2
Yan, H.G.3
Lopez-Barcons, L.4
Keller, S.M.5
Perez-Soler, R.6
Horwitz, S.B.7
McDaid, H.M.8
-
302
-
-
79953169191
-
Benefits of mTOR kinase targeting in oncology: pre-clinical evidence with AZD8055
-
Marshall G, Howard Z, Dry J, Fenton S, Heathcote D, Gray N, Keen H, Logie A, Holt S, Smith P, Guichard SM. Benefits of mTOR kinase targeting in oncology: pre-clinical evidence with AZD8055. Biochem Soc Trans. 2011; 39: 456-459.
-
(2011)
Biochem Soc Trans.
, vol.39
, pp. 456-459
-
-
Marshall, G.1
Howard, Z.2
Dry, J.3
Fenton, S.4
Heathcote, D.5
Gray, N.6
Keen, H.7
Logie, A.8
Holt, S.9
Smith, P.10
Guichard, S.M.11
-
303
-
-
77957164869
-
Antitumour activity of a potent MEK inhibitor RDEA119/BAY 869766 combined with rapamycin in human orthotopic primary pancreatic cancer xenografts
-
Chang Q, Chapman MS, Miner JN, Hedley DW. Antitumour activity of a potent MEK inhibitor RDEA119/BAY 869766 combined with rapamycin in human orthotopic primary pancreatic cancer xenografts. BMC Cancer. 2010; 10: 515.
-
(2010)
BMC Cancer.
, vol.10
, pp. 515
-
-
Chang, Q.1
Chapman, M.S.2
Miner, J.N.3
Hedley, D.W.4
-
304
-
-
63449109698
-
Myeloma cell growth inhibition is augmented by synchronous inhibition of the insulin-like growth factor 1 receptor by NVP AEW541 and inhibition of mammalian target of rapamycin by Rad001
-
Baumann P, Hagemeier H, Mandl-Weber S, Franke D, Schmidmaier R. Myeloma cell growth inhibition is augmented by synchronous inhibition of the insulin-like growth factor 1 receptor by NVP AEW541 and inhibition of mammalian target of rapamycin by Rad001. Anticancer Drugs. 2009; 20: 259-266.
-
(2009)
Anticancer Drugs.
, vol.20
, pp. 259-266
-
-
Baumann, P.1
Hagemeier, H.2
Mandl-Weber, S.3
Franke, D.4
Schmidmaier, R.5
-
305
-
-
33644877965
-
Disruption of parallel and converging signaling pathways contributes to the synergistic antitumor effects of simultaneous mTOR and EGFR inhibition in GBM cells
-
Rao RD, Mladek AC, Lamont JD, Goble JM, Erlichman C, James CD, Sarkaria JN. Disruption of parallel and converging signaling pathways contributes to the synergistic antitumor effects of simultaneous mTOR and EGFR inhibition in GBM cells. Neoplasia. 2005; 7: 921-929.
-
(2005)
Neoplasia.
, vol.7
, pp. 921-929
-
-
Rao, R.D.1
Mladek, A.C.2
Lamont, J.D.3
Goble, J.M.4
Erlichman, C.5
James, C.D.6
Sarkaria, J.N.7
-
306
-
-
77950788603
-
Dual inhibition of Akt/mammalian target of rapamycin pathway by nanoparticle albumin bound rapamycin andperifosine induces antitumor activity in multiple myeloma
-
Cirstea, D. Hideshima T, Rodig S, Santo L, Pozzi S, Vallet S, Ikeda H, Perrone G, Gorgun G, Patel K, Desai N, Sportelli P, Kapoor S, Vali S, Mukherjee S, Munshi NC, et al. Dual inhibition of Akt/mammalian target of rapamycin pathway by nanoparticle albumin bound rapamycin andperifosine induces antitumor activity in multiple myeloma. Mol Cancer Ther. 2010; 9: 963-975.
-
(2010)
Mol Cancer Ther.
, vol.9
, pp. 963-975
-
-
Cirstea, D.1
Hideshima, T.2
Rodig, S.3
Santo, L.4
Pozzi, S.5
Vallet, S.6
Ikeda, H.7
Perrone, G.8
Gorgun, G.9
Patel, K.10
Desai, N.11
Sportelli, P.12
Kapoor, S.13
Vali, S.14
Mukherjee, S.15
Munshi, N.C.16
-
307
-
-
84863012433
-
Antitumor activity of BRAF inhibitor vemurafenib in preclinical models of BRAFmutant colorectal cancer
-
Yang H, Higgins B, Kolinsky K, Packman K, Bradley WD, Lee RJ, Schostack K, Simcox ME, Kopetz S, Heimbrook D, Lestini B, Bollag G, Su F. Antitumor activity of BRAF inhibitor vemurafenib in preclinical models of BRAFmutant colorectal cancer. Cancer Res. 2012; 72: 779-789.
-
(2012)
Cancer Res.
, vol.72
, pp. 779-789
-
-
Yang, H.1
Higgins, B.2
Kolinsky, K.3
Packman, K.4
Bradley, W.D.5
Lee, R.J.6
Schostack, K.7
Simcox, M.E.8
Kopetz, S.9
Heimbrook, D.10
Lestini, B.11
Bollag, G.12
Su, F.13
-
308
-
-
84860533156
-
The heat shock protein-90 inhibitor XL888 overcomes BRAF inhibitor resistance mediated through diverse mechanisms
-
Paraiso KH, Haarberg E, Wood E, Rebecca VW, Chen YA, Xiang Y, Ribas A, Lo RS, Weber JS, Sondak VK, John J, Sarnaik AA, Koomen J, Smalley KS. The heat shock protein-90 inhibitor XL888 overcomes BRAF inhibitor resistance mediated through diverse mechanisms. Clin Cancer Res. 2012; 18: 2502-2514.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 2502-2514
-
-
Paraiso, K.H.1
Haarberg, E.2
Wood, E.3
Rebecca, V.W.4
Chen, Y.A.5
Xiang, Y.6
Ribas, A.7
Lo, R.S.8
Weber, J.S.9
Sondak, V.K.10
John, J.11
Sarnaik, A.A.12
Koomen, J.13
Smalley, K.S.14
-
309
-
-
84872805948
-
GDC-0941: A first-in-human phase Ib study testing daily and intermittent dosing schedules in patients with advanced solid tumors
-
abstr 3005
-
Shapiro G, LoRusso P, Kwak EL, Cleary JM, Musib L, Jones C, de Crespigny A, Belvin M, McKenzie M, Gates MR, Chan IT, Bendell JC. GDC-0941: A first-in-human phase Ib study testing daily and intermittent dosing schedules in patients with advanced solid tumors. J Clin Oncol. 2011; 29: (suppl; abstr 3005).
-
(2011)
J Clin Oncol.
, vol.29
, Issue.SUPPL
-
-
Shapiro, G.1
LoRusso, P.2
Kwak, E.L.3
Cleary, J.M.4
Musib, L.5
Jones, C.6
de Crespigny, A.7
Belvin, M.8
Mckenzie, M.9
Gates, M.R.10
Chan, I.T.11
Bendell, J.C.12
-
310
-
-
33646272204
-
Chemotherapy and targeted therapy combinations in advanced melanoma
-
Flaherty KT. Chemotherapy and targeted therapy combinations in advanced melanoma. Clin Cancer Res. 2006; 12: 2366s-2370s.
-
(2006)
Clin Cancer Res.
, vol.12
-
-
Flaherty, K.T.1
-
311
-
-
78650349223
-
Do predictive signatures really predict response to cancer chemotherapy?
-
Borst P, Wessels L. Do predictive signatures really predict response to cancer chemotherapy? Cell Cycle. 2010; 9: 4836-4840.
-
(2010)
Cell Cycle
, vol.9
, pp. 4836-4840
-
-
Borst, P.1
Wessels, L.2
-
312
-
-
77958481191
-
The CINSARC signature: prognostic and predictive of response to chemotherapy?
-
Bertucci F, Finetti P, Sabatier R, Birnbaum D. The CINSARC signature: prognostic and predictive of response to chemotherapy? Cell Cycle. 2010; 9: 4025-4027.
-
(2010)
Cell Cycle
, vol.9
, pp. 4025-4027
-
-
Bertucci, F.1
Finetti, P.2
Sabatier, R.3
Birnbaum, D.4
-
313
-
-
79551544267
-
PRIMA-1Met/ APR-246 induces wild-type p53-dependent suppression of malignant melanoma tumor growth in 3D culture and in vivo
-
Bao W, Chen M, Zhao X, Kumar R, Spinnler C, Thullberg M, Issaeva N, Selivanova G, Stromblad S. PRIMA-1Met/ APR-246 induces wild-type p53-dependent suppression of malignant melanoma tumor growth in 3D culture and in vivo. Cell Cycle. 2011; 10: 301-307.
-
(2011)
Cell Cycle.
, vol.10
, pp. 301-307
-
-
Bao, W.1
Chen, M.2
Zhao, X.3
Kumar, R.4
Spinnler, C.5
Thullberg, M.6
Issaeva, N.7
Selivanova, G.8
Stromblad, S.9
-
314
-
-
78649882284
-
Fasting and differential chemotherapy protection in patients
-
Raffaghello L, Safdie F, Bianchi G, Dorff T, Fontana L, Longo VD. Fasting and differential chemotherapy protection in patients. Cell Cycle. 2010; 9: 4474-4476.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4474-4476
-
-
Raffaghello, L.1
Safdie, F.2
Bianchi, G.3
Dorff, T.4
Fontana, L.5
Longo, V.D.6
-
315
-
-
79952113981
-
Cytokines shape chemotherapy-induced and 'bystander' senescence
-
Hodny Z, Hubackova S, Bartek J. Cytokines shape chemotherapy-induced and 'bystander' senescence. Aging. 2010; 2: 375-376.
-
(2010)
Aging.
, vol.2
, pp. 375-376
-
-
Hodny, Z.1
Hubackova, S.2
Bartek, J.3
-
316
-
-
80052944398
-
Schedule-dependent synergy of histone deacetylase inhibitors with DNA damaging agents in small cell lung cancer
-
Luchenko VL, Salcido CD, Zhang Y, Agama K, Komlodi-Pasztor E, Murphy RF, Giaccone G, Pommier Y, Bates SE, Varticovski L. Schedule-dependent synergy of histone deacetylase inhibitors with DNA damaging agents in small cell lung cancer. Cell Cycle. 2011; 10: 3119-3128.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3119-3128
-
-
Luchenko, V.L.1
Salcido, C.D.2
Zhang, Y.3
Agama, K.4
Komlodi-Pasztor, E.5
Murphy, R.F.6
Giaccone, G.7
Pommier, Y.8
Bates, S.E.9
Varticovski, L.10
-
317
-
-
80052054210
-
Personalizing therapy with targeted agents in non-small cell lung cancer
-
Dienstmann R, Martinez P, Felip E. Personalizing therapy with targeted agents in non-small cell lung cancer. Oncotarget. 2011; 2: 165-177.
-
(2011)
Oncotarget.
, vol.2
, pp. 165-177
-
-
Dienstmann, R.1
Martinez, P.2
Felip, E.3
-
318
-
-
84859725212
-
Protection of acute myeloid leukaemia cells from apoptosis induced by front-line chemotherapeutics is mediated by haem oxygenase-1
-
Heasman SA, Zaitseva L, Bowles KM, Rushworth SA, Macewan DJ. Protection of acute myeloid leukaemia cells from apoptosis induced by front-line chemotherapeutics is mediated by haem oxygenase-1. Oncotarget. 2011; 2: 658-668.
-
(2011)
Oncotarget.
, vol.2
, pp. 658-668
-
-
Heasman, S.A.1
Zaitseva, L.2
Bowles, K.M.3
Rushworth, S.A.4
Macewan, D.J.5
-
319
-
-
84863189306
-
Curtailing side effects in chemotherapy: a tale of PKCdelta in cisplatin treatment
-
Pabla N, Dong Z. Curtailing side effects in chemotherapy: a tale of PKCdelta in cisplatin treatment. Oncotarget. 2012; 3: 107-111.
-
(2012)
Oncotarget.
, vol.3
, pp. 107-111
-
-
Pabla, N.1
Dong, Z.2
-
320
-
-
84860334111
-
A combination of a ribonucleotide reductase inhibitor and histone deacetylase inhibitors downregulates EGFR and triggers BIM-dependent apoptosis in head and neck cancer
-
Stauber RH, Knauer SK, Habtemichael N, Bier C, Unruhe B, Weisheit S, Spange S, Nonnenmacher F, Fetz V, Ginter T, Reichardt S, Liebmann C, Schneider G, Kramer OH. A combination of a ribonucleotide reductase inhibitor and histone deacetylase inhibitors downregulates EGFR and triggers BIM-dependent apoptosis in head and neck cancer. Oncotarget. 2012; 3: 31-43.
-
(2012)
Oncotarget.
, vol.3
, pp. 31-43
-
-
Stauber, R.H.1
Knauer, S.K.2
Habtemichael, N.3
Bier, C.4
Unruhe, B.5
Weisheit, S.6
Spange, S.7
Nonnenmacher, F.8
Fetz, V.9
Ginter, T.10
Reichardt, S.11
Liebmann, C.12
Schneider, G.13
Kramer, O.H.14
-
321
-
-
84863215537
-
Polo Like kinase 2 tumour suppressor and cancer biomarker: new perspectives on drug sensitivity/resistance in ovarian cancer
-
Coley HM, Hatzimichael E, Blagden S, McNeish I, Thompson A, Crook T, Syed N. Polo Like kinase 2 tumour suppressor and cancer biomarker: new perspectives on drug sensitivity/resistance in ovarian cancer. Oncotarget. 2012; 3: 78-83.
-
(2012)
Oncotarget.
, vol.3
, pp. 78-83
-
-
Coley, H.M.1
Hatzimichael, E.2
Blagden, S.3
McNeish, I.4
Thompson, A.5
Crook, T.6
Syed, N.7
-
322
-
-
74549171725
-
The long unwinding road: XPB and XPD helicases in damaged DNA opening
-
Oksenych V, Coin F. The long unwinding road: XPB and XPD helicases in damaged DNA opening. Cell Cycle. 2010; 9: 90-96.
-
(2010)
Cell Cycle.
, vol.9
, pp. 90-96
-
-
Oksenych, V.1
Coin, F.2
-
323
-
-
84857709131
-
Mechanisms of chemotherapy-induced human ovarian aging: double strand DNA breaks and microvascular compromise
-
Soleimani R, Heytens E, Darzynkiewicz Z, Oktay K. Mechanisms of chemotherapy-induced human ovarian aging: double strand DNA breaks and microvascular compromise. Aging. 2011; 3: 782-793.
-
(2011)
Aging.
, vol.3
, pp. 782-793
-
-
Soleimani, R.1
Heytens, E.2
Darzynkiewicz, Z.3
Oktay, K.4
-
324
-
-
80055113762
-
Modulated microtubule dynamics enable Hklp2/Kif15 to assemble bipolar spindles
-
Florian S, Mayer TU. Modulated microtubule dynamics enable Hklp2/Kif15 to assemble bipolar spindles. Cell Cycle. 2011; 10: 3533-3544.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3533-3544
-
-
Florian, S.1
Mayer, T.U.2
-
325
-
-
77953594908
-
Substrate degradation by the anaphase promoting complex occurs during mitotic slippage
-
Lee J, Kim JA, Margolis RL, Fotedar R. Substrate degradation by the anaphase promoting complex occurs during mitotic slippage. Cell Cycle. 2010; 9: 1792-1801.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1792-1801
-
-
Lee, J.1
Kim, J.A.2
Margolis, R.L.3
Fotedar, R.4
-
326
-
-
77955721945
-
Small-molecule inducer of cancer cell polyploidy promotes apoptosis or senescence: Implications for therapy
-
Tovar C, Higgins B, Deo D, Kolinsky K, Liu JJ, Heimbrook DC, Vassilev LT. Small-molecule inducer of cancer cell polyploidy promotes apoptosis or senescence: Implications for therapy. Cell Cycle. 2010; 9: 3364-3375.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3364-3375
-
-
Tovar, C.1
Higgins, B.2
Deo, D.3
Kolinsky, K.4
Liu, J.J.5
Heimbrook, D.C.6
Vassilev, L.T.7
-
327
-
-
74949090183
-
Defective autophagy associated with LC3 puncta in epothilone-resistant cancer cells
-
Shen S, Kepp O, Martins I, Vitale I, Souquere S, Castedo M, Pierron G, Kroemer G. Defective autophagy associated with LC3 puncta in epothilone-resistant cancer cells. Cell Cycle. 2010; 9: 377-383.
-
(2010)
Cell Cycle.
, vol.9
, pp. 377-383
-
-
Shen, S.1
Kepp, O.2
Martins, I.3
Vitale, I.4
Souquere, S.5
Castedo, M.6
Pierron, G.7
Kroemer, G.8
-
328
-
-
84859562694
-
Targeting autophagy addiction in cancer
-
Mancias JD, Kimmelman AC. Targeting autophagy addiction in cancer. Oncotarget. 2011; 2: 1302-1306.
-
(2011)
Oncotarget.
, vol.2
, pp. 1302-1306
-
-
Mancias, J.D.1
Kimmelman, A.C.2
-
329
-
-
84858428443
-
Propranolol potentiates the anti-angiogenic effects and anti-tumor efficacy of chemotherapy agents: implication in breast cancer treatment
-
Pasquier E, Ciccolini J, Carre M, Giacometti S, Fanciullino R, Pouchy C, Montero MP, Serdjebi C, Kavallaris M, Andre N. Propranolol potentiates the anti-angiogenic effects and anti-tumor efficacy of chemotherapy agents: implication in breast cancer treatment. Oncotarget. 2010; 2: 797-809.
-
(2010)
Oncotarget.
, vol.2
, pp. 797-809
-
-
Pasquier, E.1
Ciccolini, J.2
Carre, M.3
Giacometti, S.4
Fanciullino, R.5
Pouchy, C.6
Montero, M.P.7
Serdjebi, C.8
Kavallaris, M.9
Andre, N.10
-
330
-
-
74949120328
-
Blocking ovarian cancer progression by targeting tumor microenvironmental leukocytes
-
Cubillos-Ruiz JR, Rutkowski M, Conejo-Garcia JR. Blocking ovarian cancer progression by targeting tumor microenvironmental leukocytes. Cell Cycle. 2010; 9: 260-268.
-
(2010)
Cell Cycle.
, vol.9
, pp. 260-268
-
-
Cubillos-Ruiz, J.R.1
Rutkowski, M.2
Conejo-Garcia, J.R.3
-
331
-
-
84865273469
-
Thyrocyte-specific inactivation of p53 and Pten results in anaplastic thyroid carcinomas faithfully recapitulating human tumors
-
Antico Arciuch VG, Russo MA, Dima M, Kang KS, Dasrath F, Liao XH, Refetoff S, Montagna C, Di Cristofano A. Thyrocyte-specific inactivation of p53 and Pten results in anaplastic thyroid carcinomas faithfully recapitulating human tumors. Oncotarget. 2011; 2: 1109-1126.
-
(2011)
Oncotarget.
, vol.2
, pp. 1109-1126
-
-
Arciuch, V.G.A.1
Russo, M.A.2
Dima, M.3
Kang, K.S.4
Dasrath, F.5
Liao, X.H.6
Refetoff, S.7
Montagna, C.8
Di Cristofano, A.9
-
332
-
-
79960468258
-
Exploiting p53 status to enhance effectiveness of chemotherapy by lowering associated toxicity
-
Steelman LS, Martelli AM, Nicoletti F, McCubrey JA. Exploiting p53 status to enhance effectiveness of chemotherapy by lowering associated toxicity. Oncotarget. 2011; 2: 109-112.
-
(2011)
Oncotarget.
, vol.2
, pp. 109-112
-
-
Steelman, L.S.1
Martelli, A.M.2
Nicoletti, F.3
McCubrey, J.A.4
-
333
-
-
79956035239
-
Evaluation of an Actinomycin D/ VX-680 aurora kinase inhibitor combination in p53-based cyclotherapy
-
Rao B, van Leeuwen IM, Higgins M, Campbel J, Thompson AM, Lane DP, Lain S. Evaluation of an Actinomycin D/ VX-680 aurora kinase inhibitor combination in p53-based cyclotherapy. Oncotarget. 2010; 1: 639-650.
-
(2010)
Oncotarget.
, vol.1
, pp. 639-650
-
-
Rao, B.1
van Leeuwen, I.M.2
Higgins, M.3
Campbel, J.4
Thompson, A.M.5
Lane, D.P.6
Lain, S.7
-
334
-
-
84862987210
-
Selenium is a modulator of circadian clock that protects mice from the toxicity of a chemotherapeutic drug via upregulation of the core clock protein, BMAL1
-
Hu Y, Spengler ML, Kuropatwinski KK, Comas-Soberats M, Jackson M, Chernov MV, Gleiberman AS, Fedtsova N, Rustum YM, Gudkov AV, Antoch MP. Selenium is a modulator of circadian clock that protects mice from the toxicity of a chemotherapeutic drug via upregulation of the core clock protein, BMAL1. Oncotarget. 2011; 2: 1279-1290.
-
(2011)
Oncotarget.
, vol.2
, pp. 1279-1290
-
-
Hu, Y.1
Spengler, M.L.2
Kuropatwinski, K.K.3
Comas-Soberats, M.4
Jackson, M.5
Chernov, M.V.6
Gleiberman, A.S.7
Fedtsova, N.8
Rustum, Y.M.9
Gudkov, A.V.10
Antoch, M.P.11
-
335
-
-
79960235543
-
Roles of the Ras/Raf/MEK/ ERK pathway in leukemia therapy
-
Steelman LS, Franklin RA, Abrams SL, Chappell W, Kempf CR, Bäsecke J, Stivala F, Donia M, Fagone P, Nicoletti F, Libra M, Ruvolo P, Ruvolo V, Evangelisti C, Martelli AM, McCubrey JA. Roles of the Ras/Raf/MEK/ ERK pathway in leukemia therapy. Leukemia. 2011; 25: 1080-1094.
-
(2011)
Leukemia.
, vol.25
, pp. 1080-1094
-
-
Steelman, L.S.1
Franklin, R.A.2
Abrams, S.L.3
Chappell, W.4
Kempf, C.R.5
Bäsecke, J.6
Stivala, F.7
Donia, M.8
Fagone, P.9
Nicoletti, F.10
Libra, M.11
Ruvolo, P.12
Ruvolo, V.13
Evangelisti, C.14
Martelli, A.M.15
Mccubrey, J.A.16
-
336
-
-
16844386676
-
Enhancement of the therapeutic efficacy of taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants
-
McDaid HM, Lopez-Barcons L, Grossman A, Lia M, Keller S, Pérez-Soler R, Horwitz SB. Enhancement of the therapeutic efficacy of taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants. Cancer Res. 2005; 65: 2854-2860.
-
(2005)
Cancer Res.
, vol.65
, pp. 2854-2860
-
-
Mcdaid, H.M.1
Lopez-Barcons, L.2
Grossman, A.3
Lia, M.4
Keller, S.5
Pérez-Soler, R.6
Horwitz, S.B.7
-
337
-
-
40749124035
-
The mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor AZD6244 (ARRY 142886) induces growth arrest in melanoma cells and tumor regression when combined with docetaxel
-
Haass NK, Sproesser K, Nguyen TK, Contractor R, Medina CA, Nathanson KL, Herlyn M, Smalley KS. The mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor AZD6244 (ARRY 142886) induces growth arrest in melanoma cells and tumor regression when combined with docetaxel. Clin Cancer Res. 2008; 14: 230-239.
-
(2008)
Clin Cancer Res.
, vol.14
, pp. 230-239
-
-
Haass, N.K.1
Sproesser, K.2
Nguyen, T.K.3
Contractor, R.4
Medina, C.A.5
Nathanson, K.L.6
Herlyn, M.7
Smalley, K.S.8
-
338
-
-
84857079709
-
Preclinical activity of the rational combination of selumetinib (AZD6244) in combination with vorinostat in KRAS-mutant colorectal cancer models
-
Morelli MP, Tentler JJ, Kulikowski GN, Tan AC, Bradshaw-Pierce EL, Pitts TM, Brown AM, Nallapareddy S, Arcaroli JJ, Serkova NJ, Hidalgo M, Ciardiello F, Eckhardt SG. Preclinical activity of the rational combination of selumetinib (AZD6244) in combination with vorinostat in KRAS-mutant colorectal cancer models. Clinical Cancer Research. 2012; 18: 1051-1062.
-
(2012)
Clinical Cancer Research.
, vol.18
, pp. 1051-1062
-
-
Morelli, M.P.1
Tentler, J.J.2
Kulikowski, G.N.3
Tan, A.C.4
Bradshaw-Pierce, E.L.5
Pitts, T.M.6
Brown, A.M.7
Nallapareddy, S.8
Arcaroli, J.J.9
Serkova, N.J.10
Hidalgo, M.11
Ciardiello, F.12
Eckhardt, S.G.13
-
339
-
-
77954615408
-
MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
-
Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, Tsujioka K, Ueno Y, Hatch H, Majumder PK, Pan BS, Kotani H. MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo. Mol Cancer Ther. 2010; 9: 1956-1967.
-
(2010)
Mol Cancer Ther.
, vol.9
, pp. 1956-1967
-
-
Hirai, H.1
Sootome, H.2
Nakatsuru, Y.3
Miyama, K.4
Taguchi, S.5
Tsujioka, K.6
Ueno, Y.7
Hatch, H.8
Majumder, P.K.9
Pan, B.S.10
Kotani, H.11
-
340
-
-
58149481284
-
The novel orally bioavailable inhibitor of phosphoinositol-3 kinase and mammalian target of rapamycin, NVP BEZ235, inhibits growth and proliferation in multiple myeloma
-
Baumann P, Mandl-Weber S, Oduncu F, Schmidmaier R. The novel orally bioavailable inhibitor of phosphoinositol-3 kinase and mammalian target of rapamycin, NVP BEZ235, inhibits growth and proliferation in multiple myeloma. Exp Cell Res. 2009; 315: 485-497.
-
(2009)
Exp Cell Res.
, vol.315
, pp. 485-497
-
-
Baumann, P.1
Mandl-Weber, S.2
Oduncu, F.3
Schmidmaier, R.4
-
341
-
-
74549164751
-
NVP BEZ235 as a new therapeutic option for sarcomas
-
Manara MC, Nicoletti G, Zambelli D, Ventura S, Guerzoni C, Landuzzi L, Lollini PL, Maira SM, Garcìa-Echeverrìa C, Mercuri M, Picci. NVP BEZ235 as a new therapeutic option for sarcomas. Clin Cancer Res. 2010; 16: 530-540.
-
(2010)
Clin Cancer Res.
, vol.16
, pp. 530-540
-
-
Manara, M.C.1
Nicoletti, G.2
Zambelli, D.3
Ventura, S.4
Guerzoni, C.5
Landuzzi, L.6
Lollini, P.L.7
Maira, S.M.8
Garcìa-Echeverrìa, C.9
Mercuri, M.P.10
-
342
-
-
79953709986
-
Targeting the mTOR kinase domain: the second generation of mTOR inhibitors
-
Zhang YJ, Duan Y, Zheng XF. Targeting the mTOR kinase domain: the second generation of mTOR inhibitors. Drug Discov Today. 2011; 16: 325-331.
-
(2011)
Drug Discov Today.
, vol.16
, pp. 325-331
-
-
Zhang, Y.J.1
Duan, Y.2
Zheng, X.F.3
-
343
-
-
57349194139
-
Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
-
Engelman JA, Chen L, Tan X, Crosby K, Guimaraes AR, Upadhyay R, Maira M, McNamara K, Perera SA, Song Y, Chirieac LR, Kaur R, Lightbown A, Simendinger J, Li T, Padera RF, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nature Med. 2008; 14: 1351-1356.
-
(2008)
Nature Med.
, vol.14
, pp. 1351-1356
-
-
Engelman, J.A.1
Chen, L.2
Tan, X.3
Crosby, K.4
Guimaraes, A.R.5
Upadhyay, R.6
Maira, M.7
Mcnamara, K.8
Perera, S.A.9
Song, Y.10
Chirieac, L.R.11
Kaur, R.12
Lightbown, A.13
Simendinger, J.14
Li, T.15
Padera, R.F.16
-
344
-
-
80052160251
-
The TORC1/ TORC2 inhibitor, Palomid 529, reduces tumor growth and sensitizes to docetaxel and cisplatin in aggressive and hormone refractory prostate cancer cells
-
Gravina GL, Marampon F, Petini F, Biordi L, Sherris D, Jannini EA, Tombolini V, Festuccia C. The TORC1/ TORC2 inhibitor, Palomid 529, reduces tumor growth and sensitizes to docetaxel and cisplatin in aggressive and hormone refractory prostate cancer cells. Endocr Relat Cancer. 2011; 18: 385-400.
-
(2011)
Endocr Relat Cancer.
, vol.18
, pp. 385-400
-
-
Gravina, G.L.1
Marampon, F.2
Petini, F.3
Biordi, L.4
Sherris, D.5
Jannini, E.A.6
Tombolini, V.7
Festuccia, C.8
-
345
-
-
62549130693
-
The novel Akt inhibitor Palomid 529 (P529) enhances the effect of radiotherapy in prostate cancer
-
Diaz R, Nguewa PA, Diaz-Gonzalez JA, Hamel E, Gonzalez-Moreno O, Catena R, Serrano D, Redrado M, Sherris D, Calvo A. The novel Akt inhibitor Palomid 529 (P529) enhances the effect of radiotherapy in prostate cancer. Br J Cancer. 2009; 100: 932-940.
-
(2009)
Br J Cancer.
, vol.100
, pp. 932-940
-
-
Diaz, R.1
Nguewa, P.A.2
Diaz-Gonzalez, J.A.3
Hamel, E.4
Gonzalez-Moreno, O.5
Catena, R.6
Serrano, D.7
Redrado, M.8
Sherris, D.9
Calvo, A.10
-
346
-
-
18544367200
-
Inhibition of phosphorylation of BAD and Raf-1 by Akt sensitizes human ovarian cancer cells to paclitaxel
-
Mabuchi S, Ohmichi M, Kimura A, Hisamoto K, Hayakawa J, Nishio Y, Adachi K, Takahashi K, Arimoto-Ishida E, Nakatsuji Y, Tasaka K, Murata Y. Inhibition of phosphorylation of BAD and Raf-1 by Akt sensitizes human ovarian cancer cells to paclitaxel. J Biol Chem. 2002; 277: 33490-33500.
-
(2002)
J Biol Chem.
, vol.277
, pp. 33490-33500
-
-
Mabuchi, S.1
Ohmichi, M.2
Kimura, A.3
Hisamoto, K.4
Hayakawa, J.5
Nishio, Y.6
Adachi, K.7
Takahashi, K.8
Arimoto-Ishida, E.9
Nakatsuji, Y.10
Tasaka, K.11
Murata, Y.12
-
347
-
-
0036719080
-
Variable apoptotic response of NSCLC cells to inhibition of the MEK/ERK pathway by small molecules or dominant negative mutants
-
Brognard J, Dennis PA. Variable apoptotic response of NSCLC cells to inhibition of the MEK/ERK pathway by small molecules or dominant negative mutants. Cell Death Differ. 2002; 9: 893-904.
-
(2002)
Cell Death Differ.
, vol.9
, pp. 893-904
-
-
Brognard, J.1
Dennis, P.A.2
-
348
-
-
3242806803
-
Cisplatin activates survival signals in UM-SCC-23 squamous cell carcinoma and these signal pathways are amplified in cisplatinresistant squamous cell carcinoma
-
Aoki K, Ogawa T, Ito Y, Nakashima S. Cisplatin activates survival signals in UM-SCC-23 squamous cell carcinoma and these signal pathways are amplified in cisplatinresistant squamous cell carcinoma. Oncol Rep. 2004; 11: 375-379.
-
(2004)
Oncol Rep.
, vol.11
, pp. 375-379
-
-
Aoki, K.1
Ogawa, T.2
Ito, Y.3
Nakashima, S.4
-
349
-
-
31844453715
-
Signalling responses linked to betulinic acid-induced apoptosis are antagonized by MEK inhibitor U0126 in adherent or 3D spheroid melanoma irrespective of p53 status
-
Rieber M, Rieber MS. Signalling responses linked to betulinic acid-induced apoptosis are antagonized by MEK inhibitor U0126 in adherent or 3D spheroid melanoma irrespective of p53 status. Int J Cancer. 2006; 118: 1135-1143.
-
(2006)
Int J Cancer.
, vol.118
, pp. 1135-1143
-
-
Rieber, M.1
Rieber, M.S.2
-
350
-
-
33947501692
-
Mammalian target of rapamycin pathway activity in hepatocellular carcinomas of patients undergoing liver transplantation
-
Sieghart W, Fuereder T, Schmid K, Cejka D, Werzowa J, Wrba F, Wang X, Gruber D, Rasoul-Rockenschaub S, Peck-Radosavljevic M, Wacheck V. Mammalian target of rapamycin pathway activity in hepatocellular carcinomas of patients undergoing liver transplantation. Transplantation. 2007; 83: 425-432.
-
(2007)
Transplantation.
, vol.83
, pp. 425-432
-
-
Sieghart, W.1
Fuereder, T.2
Schmid, K.3
Cejka, D.4
Werzowa, J.5
Wrba, F.6
Wang, X.7
Gruber, D.8
Rasoul-Rockenschaub, S.9
Peck-Radosavljevic, M.10
Wacheck, V.11
-
351
-
-
33846277588
-
In vivo inhibition of human hepatocellular carcinoma related angiogenesis by vinblastine and rapamycin
-
Ribatti D, Nico B, Mangieri D, Longo V, Sansonno D, Vacca A, Dammacco F. In vivo inhibition of human hepatocellular carcinoma related angiogenesis by vinblastine and rapamycin. Histol Histopathol. 2007; 22: 285-289.
-
(2007)
Histol Histopathol.
, vol.22
, pp. 285-289
-
-
Ribatti, D.1
Nico, B.2
Mangieri, D.3
Longo, V.4
Sansonno, D.5
Vacca, A.6
Dammacco, F.7
-
352
-
-
47949116252
-
SHARP Investigators Study Group
-
Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF, de Oliveira AC, Santoro A, Raoul JL, Forner A, Schwartz M, Porta C, Zeuzem S, Bolondi L, Greten TF, Galle PR, et al. SHARP Investigators Study Group. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med. 2008; 359: 378-390.
-
(2008)
Sorafenib in advanced hepatocellular carcinoma. N Engl J Med.
, vol.359
, pp. 378-390
-
-
Llovet, J.M.1
Ricci, S.2
Mazzaferro, V.3
Hilgard, P.4
Gane, E.5
Blanc, J.F.6
de Oliveira, A.C.7
Santoro, A.8
Raoul, J.L.9
Forner, A.10
Schwartz, M.11
Porta, C.12
Zeuzem, S.13
Bolondi, L.14
Greten, T.F.15
Galle, P.R.16
-
353
-
-
77958489008
-
Inhibitionof ATM kinase activity does not phenocopy ATM protein disruption: implications for the clinical utility of ATM kinase inhibitors
-
Choi S, Gamper AM, White JS, Bakkenist CJ. Inhibitionof ATM kinase activity does not phenocopy ATM protein disruption: implications for the clinical utility of ATM kinase inhibitors. Cell Cycle. 2010; 9: 4052-4057.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4052-4057
-
-
Choi, S.1
Gamper, A.M.2
White, J.S.3
Bakkenist, C.J.4
-
354
-
-
80055102133
-
The H2B ubiquitin ligase RNF40 cooperates with SUPT16H to induce dynamic changes in chromatin structure during DNA double-strand break repair
-
Kari V, Shchebet A, Neumann H, Johnsen SA. The H2B ubiquitin ligase RNF40 cooperates with SUPT16H to induce dynamic changes in chromatin structure during DNA double-strand break repair. Cell Cycle. 2011; 10: 3495-3504.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3495-3504
-
-
Kari, V.1
Shchebet, A.2
Neumann, H.3
Johnsen, S.A.4
-
355
-
-
79956022145
-
Restoring p53 active conformation by zinc increases the response of mutant p53 tumor cells to anticancer drugs
-
Puca R, Nardinocchi L, Porru M, Simon AJ, Rechavi G, Leonetti C, Givol D, D'Orazi G. Restoring p53 active conformation by zinc increases the response of mutant p53 tumor cells to anticancer drugs. Cell Cycle. 2011; 10: 1679-1689.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1679-1689
-
-
Puca, R.1
Nardinocchi, L.2
Porru, M.3
Simon, A.J.4
Rechavi, G.5
Leonetti, C.6
Givol, D.7
D'Orazi, G.8
-
356
-
-
77953562379
-
Rescue of the apoptotic-inducing function of mutant p53 by small molecule RITA
-
Zhao CY, Grinkevich VV, Nikulenkov F, Bao W, Selivanova G. Rescue of the apoptotic-inducing function of mutant p53 by small molecule RITA. Cell Cycle. 2010; 9: 1847-1855.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1847-1855
-
-
Zhao, C.Y.1
Grinkevich, V.V.2
Nikulenkov, F.3
Bao, W.4
Selivanova, G.5
-
357
-
-
84857129980
-
PARP inhibition sensitizes childhood high grade glioma, medulloblastoma and ependymoma to radiation
-
van Vuurden DG, Hulleman E, Meijer OL, Wedekind LE, Kool M, Witt H, Vandertop PW, Wurdinger T, Noske DP, Kaspers GJ, Cloos J. PARP inhibition sensitizes childhood high grade glioma, medulloblastoma and ependymoma to radiation. Oncotarget. 2011; 2: 984-996.
-
(2011)
Oncotarget.
, vol.2
, pp. 984-996
-
-
van Vuurden, D.G.1
Hulleman, E.2
Meijer, O.L.3
Wedekind, L.E.4
Kool, M.5
Witt, H.6
Vandertop, P.W.7
Wurdinger, T.8
Noske, D.P.9
Kaspers, G.J.10
Cloos, J.11
-
358
-
-
65649120430
-
In vitro and in vivo radiosensitization with AZD6244 (ARRY-142886), an inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinases 1 /2 kinase
-
Chung EJ, Brown AP, Asano H, Mandler M, Burgan WE, Carter D, Camphausen K, Citrin D. In vitro and in vivo radiosensitization with AZD6244 (ARRY-142886), an inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinases 1 /2 kinase. Clin Cancer Res. 2009; 15: 3050-3057.
-
(2009)
Clin Cancer Res.
, vol.15
, pp. 3050-3057
-
-
Chung, E.J.1
Brown, A.P.2
Asano, H.3
Mandler, M.4
Burgan, W.E.5
Carter, D.6
Camphausen, K.7
Citrin, D.8
-
359
-
-
80055108191
-
Chk2 deficiency in Myc overexpressing lymphoma cells elicits a synergistic lethal response in combination with PARP inhibition
-
Hoglund A, Stromvall K, Li Y, Forshell LP, Nilsson JA. Chk2 deficiency in Myc overexpressing lymphoma cells elicits a synergistic lethal response in combination with PARP inhibition. Cell Cycle. 2011; 10: 3598-3607.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3598-3607
-
-
Hoglund, A.1
Stromvall, K.2
Li, Y.3
Forshell, L.P.4
Nilsson, J.A.5
-
360
-
-
79959978644
-
Unleashing Chk1 in cancer therapy
-
Carrassa L, Damia G. Unleashing Chk1 in cancer therapy. Cell Cycle. 2011; 10: 2121-2128.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2121-2128
-
-
Carrassa, L.1
Damia, G.2
-
361
-
-
79960016115
-
Division of labor of the replication fork protection complex subunits in sister chromatid cohesion and Chk1 activation
-
Noguchi E. Division of labor of the replication fork protection complex subunits in sister chromatid cohesion and Chk1 activation. Cell Cycle. 2011; 10: 2055-2056.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2055-2056
-
-
Noguchi, E.1
-
363
-
-
77954159791
-
Mitotic DNA damage response: Polo-like kinase-1 is dephosphorylated through ATM-Chk1 pathway
-
Lee HJ, Hwang HI, Jang YJ. Mitotic DNA damage response: Polo-like kinase-1 is dephosphorylated through ATM-Chk1 pathway. Cell Cycle. 2010; 9: 2389-2398.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2389-2398
-
-
Lee, H.J.1
Hwang, H.I.2
Jang, Y.J.3
-
364
-
-
79956047381
-
Timeless functions independently of the Tim-Tipin complex to promote sister chromatid cohesion in normal human fibroblasts
-
Smith-Roe SL, Patel SS, Simpson DA, Zhou YC, Rao S, Ibrahim JG, Kaiser-Rogers KA, Cordeiro-Stone M, Kaufmann WK. Timeless functions independently of the Tim-Tipin complex to promote sister chromatid cohesion in normal human fibroblasts. Cell Cycle. 2011; 10: 1618-1624.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1618-1624
-
-
Smith-Roe, S.L.1
Patel, S.S.2
Simpson, D.A.3
Zhou, Y.C.4
Rao, S.5
Ibrahim, J.G.6
Kaiser-Rogers, K.A.7
Cordeiro-Stone, M.8
Kaufmann, W.K.9
-
365
-
-
79951919841
-
The DNA damage effector Chk1 kinase regulates Cdc14B nucleolar shuttling during cell cycle progression
-
Peddibhotla S, Wei Z, Papineni R, Lam MH, Rosen JM, Zhang P. The DNA damage effector Chk1 kinase regulates Cdc14B nucleolar shuttling during cell cycle progression. Cell Cycle. 2011; 10: 671-679.
-
(2011)
Cell Cycle.
, vol.10
, pp. 671-679
-
-
Peddibhotla, S.1
Wei, Z.2
Papineni, R.3
Lam, M.H.4
Rosen, J.M.5
Zhang, P.6
-
366
-
-
79951900140
-
Nek1 kinase functions in DNA damage response and checkpoint control through a pathway independent of ATM and ATR
-
Chen Y, Chen CF, Riley DJ, Chen PL. Nek1 kinase functions in DNA damage response and checkpoint control through a pathway independent of ATM and ATR. Cell Cycle. 2011; 10: 655-663.
-
(2011)
Cell Cycle.
, vol.10
, pp. 655-663
-
-
Chen, Y.1
Chen, C.F.2
Riley, D.J.3
Chen, P.L.4
-
367
-
-
79851498851
-
CK1epsilon targets Cdc25A for ubiquitinmediated proteolysis under normal conditions and in response to checkpoint activation
-
Piao S, Lee SJ, Xu Y, Gwak J, Oh S, Park BJ, Ha NC. CK1epsilon targets Cdc25A for ubiquitinmediated proteolysis under normal conditions and in response to checkpoint activation. Cell Cycle. 2011; 10: 531-537.
-
(2011)
Cell Cycle.
, vol.10
, pp. 531-537
-
-
Piao, S.1
Lee, S.J.2
Xu, Y.3
Gwak, J.4
Oh, S.5
Park, B.J.6
Ha, N.C.7
-
368
-
-
77953557271
-
Revised genetic requirements for the decatenation G2 checkpoint: the role of ATM
-
Bower JJ, Zhou Y, Zhou T, Simpson DA, Arlander SJ, Paules RS, Cordeiro-Stone M, Kaufmann WK. Revised genetic requirements for the decatenation G2 checkpoint: the role of ATM. Cell Cycle. 2010; 9: 1617-1628.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1617-1628
-
-
Bower, J.J.1
Zhou, Y.2
Zhou, T.3
Simpson, D.A.4
Arlander, S.J.5
Paules, R.S.6
Cordeiro-Stone, M.7
Kaufmann, W.K.8
-
369
-
-
77953493199
-
Xenopus DNA2 is a helicase/ nuclease that is found in complexes with replication proteins And-1/Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATM
-
Wawrousek KE, Fortini BK, Polaczek P, Chen L, Liu Q, Dunphy WG, Campbell JL. Xenopus DNA2 is a helicase/ nuclease that is found in complexes with replication proteins And-1/Ctf4 and Mcm10 and DSB response proteins Nbs1 and ATM. Cell Cycle. 2010; 9: 1156-1166.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1156-1166
-
-
Wawrousek, K.E.1
Fortini, B.K.2
Polaczek, P.3
Chen, L.4
Liu, Q.5
Dunphy, W.G.6
Campbell, J.L.7
-
370
-
-
77953503908
-
Targeting Chk1 in the replicative stress response
-
Dai Y, Grant S. Targeting Chk1 in the replicative stress response. Cell Cycle. 2010; 9: 1025.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1025
-
-
Dai, Y.1
Grant, S.2
-
371
-
-
77955441894
-
Centrosomal Chk2 in DNA damage responses and cell cycle progression
-
Golan A, Pick E, Tsvetkov L, Nadler Y, Kluger H, Stern DF. Centrosomal Chk2 in DNA damage responses and cell cycle progression. Cell Cycle. 2010; 9: 2647-2656.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2647-2656
-
-
Golan, A.1
Pick, E.2
Tsvetkov, L.3
Nadler, Y.4
Kluger, H.5
Stern, D.F.6
-
372
-
-
77955449974
-
Exposure to acute hypoxia induces a transient DNA damage response which includes Chk1 and TLK1
-
Pires IM, Bencokova Z, McGurk C, Hammond EM. Exposure to acute hypoxia induces a transient DNA damage response which includes Chk1 and TLK1. Cell Cycle. 2010; 9: 2502-2507.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2502-2507
-
-
Pires, I.M.1
Bencokova, Z.2
McGurk, C.3
Hammond, E.M.4
-
373
-
-
78349282593
-
FGF inhibits the activity of the cyclin B1/CDK1 kinase to induce a transient G2arrest in RCS chondrocytes
-
Kolupaeva V, Basilico C. FGF inhibits the activity of the cyclin B1/CDK1 kinase to induce a transient G2arrest in RCS chondrocytes. Cell Cycle. 2010; 9: 4379-4386.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4379-4386
-
-
Kolupaeva, V.1
Basilico, C.2
-
374
-
-
77953592731
-
A small peptide mimicking the key domain of MEPE/OF45 interacting with CHK1 protects human cells from radiationinduced killing
-
Yu X, Wang H, Liu S, Zhang X, Guida P, Hu B, Wang Y. A small peptide mimicking the key domain of MEPE/OF45 interacting with CHK1 protects human cells from radiationinduced killing. Cell Cycle. 2010; 9: 1981-1985.
-
(2010)
Cell Cycle.
, vol.9
, pp. 1981-1985
-
-
Yu, X.1
Wang, H.2
Liu, S.3
Zhang, X.4
Guida, P.5
Hu, B.6
Wang, Y.7
-
375
-
-
77958486280
-
APC/C(Cdc20) targets E2F1 for degradation in prometaphase
-
Peart MJ, Poyurovsky MV, Kass EM, Urist M, Verschuren EW. Summers MK. Jackson PK. Prives C. APC/C(Cdc20) targets E2F1 for degradation in prometaphase. Cell Cycle. 2010; 9: 3956-3964.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3956-3964
-
-
Peart, M.J.1
Poyurovsky, M.V.2
Kass, E.M.3
Urist, M.4
Verschuren, E.W.5
Summers, M.K.6
Jackson, P.K.7
Prives, C.8
-
376
-
-
77956847219
-
MCL-1 localizes to sites of DNA damage and regulates DNA damage response
-
Jamil S, Stoica C, Hackett TL, Duronio V. MCL-1 localizes to sites of DNA damage and regulates DNA damage response. Cell Cycle. 2010; 9: 2843-2855.
-
(2010)
Cell Cycle.
, vol.9
, pp. 2843-2855
-
-
Jamil, S.1
Stoica, C.2
Hackett, T.L.3
Duronio, V.4
-
377
-
-
77955720762
-
Deregulated Ras signaling compromises DNA damage checkpoint recovery in S
-
Wood MD, Sanchez Y. Deregulated Ras signaling compromises DNA damage checkpoint recovery in S. cerevisiae. Cell Cycle. 2010; 9: 3353-3363.
-
(2010)
cerevisiae. Cell Cycle.
, vol.9
, pp. 3353-3363
-
-
Wood, M.D.1
Sanchez, Y.2
-
378
-
-
77953506262
-
Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase
-
McNeely S, Conti C, Sheikh T, Patel H, Zabludoff S, Pommier Y, Schwartz G, Tse A. Chk1 inhibition after replicative stress activates a double strand break response mediated by ATM and DNA-dependent protein kinase. Cell Cycle. 2010; 9: 995-1004.
-
(2010)
Cell Cycle.
, vol.9
, pp. 995-1004
-
-
Mcneely, S.1
Conti, C.2
Sheikh, T.3
Patel, H.4
Zabludoff, S.5
Pommier, Y.6
Schwartz, G.7
Tse, A.8
-
379
-
-
77951921883
-
NEK11: linking CHK1 and CDC25A in DNA damage checkpoint signaling
-
Sorensen CS, Melixetian M, Klein DK, Helin K. NEK11: linking CHK1 and CDC25A in DNA damage checkpoint signaling. Cell Cycle. 2010; 9: 450-455.
-
(2010)
Cell Cycle.
, vol.9
, pp. 450-455
-
-
Sorensen, C.S.1
Melixetian, M.2
Klein, D.K.3
Helin, K.4
-
380
-
-
77951894248
-
The Rad9A checkpoint protein is required for nuclear localization of the claspin adaptor protein
-
Sierant ML, Archer NE, Davey SK. The Rad9A checkpoint protein is required for nuclear localization of the claspin adaptor protein. Cell Cycle. 2010; 9: 548-556.
-
(2010)
Cell Cycle.
, vol.9
, pp. 548-556
-
-
Sierant, M.L.1
Archer, N.E.2
Davey, S.K.3
-
381
-
-
74949093067
-
A role for Chk2 in DNA damage induced mitotic delays in human colorectal cancer cells
-
Varmark H, Kwak S, Theurkauf WE. A role for Chk2 in DNA damage induced mitotic delays in human colorectal cancer cells. Cell Cycle. 2010; 9: 312-320.
-
(2010)
Cell Cycle.
, vol.9
, pp. 312-320
-
-
Varmark, H.1
Kwak, S.2
Theurkauf, W.E.3
-
382
-
-
74949120032
-
Targeting the checkpoint kinase Chk1 in cancer therapy
-
Merry C, Fu K, Wang J, Yeh IJ, Zhang Y. Targeting the checkpoint kinase Chk1 in cancer therapy. Cell Cycle. 2010; 9: 279-283.
-
(2010)
Cell Cycle.
, vol.9
, pp. 279-283
-
-
Merry, C.1
Fu, K.2
Wang, J.3
Yeh, I.J.4
Zhang, Y.5
-
383
-
-
74549186666
-
Processing of O6-methylguanine into DNA double-strand breaks requires two rounds of replication whereas apoptosis is also induced in subsequent cell cycles
-
Quiros S, Roos WP, Kaina B. Processing of O6-methylguanine into DNA double-strand breaks requires two rounds of replication whereas apoptosis is also induced in subsequent cell cycles. Cell Cycle. 2010; 9: 168-178.
-
(2010)
Cell Cycle.
, vol.9
, pp. 168-178
-
-
Quiros, S.1
Roos, W.P.2
Kaina, B.3
-
384
-
-
0037102157
-
Phosphatidylinositol 3-kinase/Akt signaling in the response to vascular endothelium to ionizing radiation
-
Edwards E, Geng L, Tan J, Onishko H, Donnelly E, Hallahan DE. Phosphatidylinositol 3-kinase/Akt signaling in the response to vascular endothelium to ionizing radiation. Cancer Res. 2002; 62: 4671-4677.
-
(2002)
Cancer Res.
, vol.62
, pp. 4671-4677
-
-
Edwards, E.1
Geng, L.2
Tan, J.3
Onishko, H.4
Donnelly, E.5
Hallahan, D.E.6
-
385
-
-
24644447853
-
Enhanced radiation damage of tumor vasculature by mTOR inhibitors
-
Shinohara ET, Cao C, Niermann K, Mu Y, Zeng F, Hallahan DE, Lu B. Enhanced radiation damage of tumor vasculature by mTOR inhibitors. Oncogene. 2005; 24: 5414-5422.
-
(2005)
Oncogene.
, vol.24
, pp. 5414-5422
-
-
Shinohara, E.T.1
Cao, C.2
Niermann, K.3
Mu, Y.4
Zeng, F.5
Hallahan, D.E.6
Lu, B.7
-
386
-
-
28244475972
-
Rapamycin-sensitive pathway regulates mitochondrial membrane potential, autophagy, and survival in irradiated MCF-7 cells
-
Paglin S, Lee NY, Nakar C, Fitzgerald M, Plotkin J, Deuel B, Hackett N, McMahill M, Sphicas E, Lampen N, Yahalom J. Rapamycin-sensitive pathway regulates mitochondrial membrane potential, autophagy, and survival in irradiated MCF-7 cells. Cancer Res. 2005; 65: 11061-11070.
-
(2005)
Cancer Res.
, vol.65
, pp. 11061-11070
-
-
Paglin, S.1
Lee, N.Y.2
Nakar, C.3
Fitzgerald, M.4
Plotkin, J.5
Deuel, B.6
Hackett, N.7
McMahill, M.8
Sphicas, E.9
Lampen, N.10
Yahalom, J.11
-
387
-
-
33947417275
-
Crosstalk between Bak/Bax and mTOR signaling regulates radiation induced autophagy
-
Moretti L, Attia A, Kim KW, Lu B. Crosstalk between Bak/Bax and mTOR signaling regulates radiation induced autophagy. Autophagy. 2007; 3: 142-144.
-
(2007)
Autophagy.
, vol.3
, pp. 142-144
-
-
Moretti, L.1
Attia, A.2
Kim, K.W.3
Lu, B.4
-
389
-
-
79961099905
-
From growing to secreting: new roles for mTOR in aging cells
-
Pani G. From growing to secreting: new roles for mTOR in aging cells. Cell Cycle. 2011; 10: 2450-2453.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2450-2453
-
-
Pani, G.1
-
390
-
-
80051727367
-
Inflammation and autophagy conspire to promote tumor growth
-
Korkaya H, Wicha MS. Inflammation and autophagy conspire to promote tumor growth. Cell Cycle. 2011; 10: 2623-2624.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2623-2624
-
-
Korkaya, H.1
Wicha, M.S.2
-
391
-
-
80052415530
-
Coordinated epigenetic regulation of autophagy and apoptosis
-
Boehrer S, Lainey E, Kroemer G. Coordinated epigenetic regulation of autophagy and apoptosis. Cell Cycle. 2011; 10: 2832-2833.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2832-2833
-
-
Boehrer, S.1
Lainey, E.2
Kroemer, G.3
-
392
-
-
77957002198
-
Starved cells use mitochondria for autophagosome biogenesis
-
Rambold AS, Lippincott-Schwartz J. Starved cells use mitochondria for autophagosome biogenesis. Cell Cycle. 2010; 9: 3633-3634.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3633-3634
-
-
Rambold, A.S.1
Lippincott-Schwartz, J.2
-
393
-
-
74949138902
-
Defective autophagy control by the p53 rheostat in cancer
-
Galluzzi L, Morselli E, Kepp O, Maiuri MC, Kroemer G. Defective autophagy control by the p53 rheostat in cancer. Cell Cycle. 2010; 9: 250-255.
-
(2010)
Cell Cycle.
, vol.9
, pp. 250-255
-
-
Galluzzi, L.1
Morselli, E.2
Kepp, O.3
Maiuri, M.C.4
Kroemer, G.5
-
394
-
-
77956402268
-
Targeting autophagy to fight hematopoietic malignancies
-
Puissant A, Robert G, Auberger P. Targeting autophagy to fight hematopoietic malignancies. Cell Cycle. 2010; 9: 3470-3478.
-
(2010)
Cell Cycle.
, vol.9
, pp. 3470-3478
-
-
Puissant, A.1
Robert, G.2
Auberger, P.3
-
395
-
-
79960457766
-
Azacitidine-resistant SKM1 myeloid cells are defective for AZA-induced mitochondrial apoptosis and autophagy
-
Cluzeau T, Robert G, Puissant A, Jean-Michel K, Cassuto JP, Raynaud S, Auberger P. Azacitidine-resistant SKM1 myeloid cells are defective for AZA-induced mitochondrial apoptosis and autophagy. Cell Cycle. 2011; 10: 2339-2343.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2339-2343
-
-
Cluzeau, T.1
Robert, G.2
Puissant, A.3
Jean-Michel, K.4
Cassuto, J.P.5
Raynaud, S.6
Auberger, P.7
-
396
-
-
79957901938
-
Autophagy in the pathogenesis of myelodysplastic syndrome and acute myeloid leukemia
-
Watson AS, Mortensen M, Simon AK. Autophagy in the pathogenesis of myelodysplastic syndrome and acute myeloid leukemia. Cell Cycle. 2011; 10: 1719-1725.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1719-1725
-
-
Watson, A.S.1
Mortensen, M.2
Simon, A.K.3
-
397
-
-
78349266054
-
The autophagic tumor stroma model of cancer or "batteryoperated tumor growth": A simple solution to the autophagy paradox
-
Martinez-Outschoorn UE, Whitaker-Menezes D, Pavlides S, Chiavarina B, Bonuccelli G, Casey T, Tsirigos A, Migneco G, Witkiewicz A, Balliet R, Mercier I, Wang C, Flomenberg N, Howell A, Lin Z, Caro J, et al. The autophagic tumor stroma model of cancer or "batteryoperated tumor growth": A simple solution to the autophagy paradox. Cell Cycle. 2010; 9: 4297-4306.
-
(2010)
Cell Cycle.
, vol.9
, pp. 4297-4306
-
-
Martinez-Outschoorn, U.E.1
Whitaker-Menezes, D.2
Pavlides, S.3
Chiavarina, B.4
Bonuccelli, G.5
Casey, T.6
Tsirigos, A.7
Migneco, G.8
Witkiewicz, A.9
Balliet, R.10
Mercier, I.11
Wang, C.12
Flomenberg, N.13
Howell, A.14
Lin, Z.15
Caro, J.16
-
398
-
-
79959282414
-
Matrix remodeling stimulates stromal autophagy, "fueling" cancer cell mitochondrial metabolism and metastasis
-
Castello-Cros R, Bonuccelli G, Molchansky A, Capozza F, Witkiewicz AK, Birbe RC, Howell A, Pestell RG, Whitaker-Menezes D, Sotgia F, Lisanti MP. Matrix remodeling stimulates stromal autophagy, "fueling" cancer cell mitochondrial metabolism and metastasis. Cell Cycle. 2011; 10: 2021-2034.
-
(2011)
Cell Cycle.
, vol.10
, pp. 2021-2034
-
-
Castello-Cros, R.1
Bonuccelli, G.2
Molchansky, A.3
Capozza, F.4
Witkiewicz, A.K.5
Birbe, R.C.6
Howell, A.7
Pestell, R.G.8
Whitaker-Menezes, D.9
Sotgia, F.10
Lisanti, M.P.11
-
399
-
-
80053437523
-
Autophagic tumor stroma: a biofuel for cancer growth
-
Iozzo RV. Autophagic tumor stroma: a biofuel for cancer growth. Cell Cycle. 2011; 10: 3231-3232.
-
(2011)
Cell Cycle.
, vol.10
, pp. 3231-3232
-
-
Iozzo, R.V.1
-
400
-
-
36048963331
-
Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance
-
Zhou J, Wulkuhle J, Zhang H, Gu P, Yang Y, Deng J, Margolick JB, Liotta LA, Petricoin E 3rd, Zhang Y. Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance. roc Natl Acad Sci USA. 2007; 104: 16158-16163.
-
(2007)
roc Natl Acad Sci USA.
, vol.104
, pp. 16158-16163
-
-
Zhou, J.1
Wulkuhle, J.2
Zhang, H.3
Gu, P.4
Yang, Y.5
Deng, J.6
Margolick, J.B.7
Liotta, L.A.8
Petricoin, E.9
Zhang, Y.10
-
401
-
-
77957994045
-
Perspectives on inhibiting mTOR as a future treatment strategy for hematological malignancies
-
Chapuis N, Tamburini J, Green AS, Willems L, Bardet V, Park S, Lacombe C, Mayeux P, Bouscary D. Perspectives on inhibiting mTOR as a future treatment strategy for hematological malignancies. Leukemia. 2010; 24: 1686-1699.
-
(2010)
Leukemia.
, vol.24
, pp. 1686-1699
-
-
Chapuis, N.1
Tamburini, J.2
Green, A.S.3
Willems, L.4
Bardet, V.5
Park, S.6
Lacombe, C.7
Mayeux, P.8
Bouscary, D.9
-
402
-
-
79959353534
-
Targeting the phosphatidylinositol 3-kinase/Akt/ mammalian target of rapamycin signaling network in cancer stem cells
-
Martelli AM, Evangelisti C, Follo MY, Ramazzotti G, Fini M, Giardino R, Manzoli L, McCubrey JA, Cocco L. Targeting the phosphatidylinositol 3-kinase/Akt/ mammalian target of rapamycin signaling network in cancer stem cells. Current Medicinal Chemistry. 2011; 18: 2715-2726.
-
(2011)
Current Medicinal Chemistry.
, vol.18
, pp. 2715-2726
-
-
Martelli, A.M.1
Evangelisti, C.2
Follo, M.Y.3
Ramazzotti, G.4
Fini, M.5
Giardino, R.6
Manzoli, L.7
Mccubrey, J.A.8
Cocco, L.9
-
403
-
-
84860146509
-
Targeting the cancer initiating Cell: The ultimate target for cancer therapy
-
McCubrey JA, Steelman LS, Abrams SL, Misaghian N, Chappell WH, Bäsecke J, Nicoletti F, Libra M, Ligresti G, Stivala F, Maksimovic-Ivanic D, Mijatovic S, Montalto G, Cervello M, Laidler P, Bonati A, et al. Targeting the cancer initiating Cell: The ultimate target for cancer therapy. Current Pharmaceutical Design. 2011; 18: 1784-1795.
-
(2011)
Current Pharmaceutical Design.
, vol.18
, pp. 1784-1795
-
-
Mccubrey, J.A.1
Steelman, L.S.2
Abrams, S.L.3
Misaghian, N.4
Chappell, W.H.5
Bäsecke, J.6
Nicoletti, F.7
Libra, M.8
Ligresti, G.9
Stivala, F.10
Maksimovic-Ivanic, D.11
Mijatovic, S.12
Montalto, G.13
Cervello, M.14
Laidler, P.15
Bonati, A.16
-
405
-
-
84859461497
-
Metformin and cancer stem cells: old drug, new targets
-
Bednar F, Simeone DM. Metformin and cancer stem cells: old drug, new targets. Cancer Prev Res. 2012; 5: 351-354.
-
(2012)
Cancer Prev Res.
, vol.5
, pp. 351-354
-
-
Bednar, F.1
Simeone, D.M.2
-
406
-
-
84859463669
-
Metformin inhibits cell proliferation, migration and invasion by attenuating CSC function mediated by deregulating miRNAs in pancreatic cancer cells
-
Phila
-
Bao B, Wang Z, Ali S, Ahmad A, Azmi AS, Sarkar SH, Banerjee S, Kong D, Li Y, Thakur S, Sarkar FH. Metformin inhibits cell proliferation, migration and invasion by attenuating CSC function mediated by deregulating miRNAs in pancreatic cancer cells. Cancer Prev Res (Phila). 2012; 5: 355-364.
-
(2012)
Cancer Prev Res
, vol.5
, pp. 355-364
-
-
Bao, B.1
Wang, Z.2
Ali, S.3
Ahmad, A.4
Azmi, A.S.5
Sarkar, S.H.6
Banerjee, S.7
Kong, D.8
Li, Y.9
Thakur, S.10
Sarkar, F.H.11
|