-
1
-
-
33746257209
-
The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism
-
Engelman JA, Luo J, Cantley LC. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet. 2006;7(8):606-619.
-
(2006)
Nat Rev Genet
, vol.7
, Issue.8
, pp. 606-619
-
-
Engelman, J.A.1
Luo, J.2
Cantley, L.C.3
-
2
-
-
29444449785
-
The oncogenic properties of mutant p110alpha and p110beta phosphatidylinositol 3-kinases in human mammary epithelial cells
-
Zhao JJ, Liu Z, Wang L, Shin E, Loda MF, Roberts TM. The oncogenic properties of mutant p110alpha and p110beta phosphatidylinositol 3-kinases in human mammary epithelial cells. Proc Natl Acad Sci U S A. 2005;102(51):18443-18448.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, Issue.51
, pp. 18443-18448
-
-
Zhao, J.J.1
Liu, Z.2
Wang, L.3
Shin, E.4
Loda, M.F.5
Roberts, T.M.6
-
3
-
-
28244479028
-
Breast cancer-associated PIK3CA mutations are oncogenic in mammary epithelial cells
-
Isakoff SJ, Engelman JA, Irie HY, Luo J, Brachmann SM, Pearline RV, Cantley LC, Brugge JS. Breast cancer-associated PIK3CA mutations are oncogenic in mammary epithelial cells. Cancer Res. 2005;65(23):10992-11000.
-
(2005)
Cancer Res
, vol.65
, Issue.23
, pp. 10992-11000
-
-
Isakoff, S.J.1
Engelman, J.A.2
Irie, H.Y.3
Luo, J.4
Brachmann, S.M.5
Pearline, R.V.6
Cantley, L.C.7
Brugge, J.S.8
-
4
-
-
14144252004
-
Phosphatidylinositol 3-kinase mutations identified in human cancer are oncogenic
-
Kang S, Bader AG, Vogt PK. Phosphatidylinositol 3-kinase mutations identified in human cancer are oncogenic. Proc Natl Acad Sci U S A. 2005;102(3):802-807.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, Issue.3
, pp. 802-807
-
-
Kang, S.1
Bader, A.G.2
Vogt, P.K.3
-
5
-
-
31944444234
-
Cancer-specific mutations in PIK3CA are oncogenic in vivo
-
Bader AG, Kang S, Vogt PK. Cancer-specific mutations in PIK3CA are oncogenic in vivo. Proc Natl Acad Sci U S A. 2006;103(5):1475-1479.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, Issue.5
, pp. 1475-1479
-
-
Bader, A.G.1
Kang, S.2
Vogt, P.K.3
-
6
-
-
13844251972
-
Lack of PTEN sequesters CHK1 and initiates genetic instability
-
Puc J, Keniry M, Li HS, Pandita TK, Choudhury AD, Memeo L, Mansukhani M, Murty VV, Gaciong Z, Meek SE, Piwnica-Worms H, Hibshoosh H, Parsons R. Lack of PTEN sequesters CHK1 and initiates genetic instability. Cancer Cell. 2005;7(2):193-204.
-
(2005)
Cancer Cell
, vol.7
, Issue.2
, pp. 193-204
-
-
Puc, J.1
Keniry, M.2
Li, H.S.3
Pandita, T.K.4
Choudhury, A.D.5
Memeo, L.6
Mansukhani, M.7
Murty, V.V.8
Gaciong, Z.9
Meek, S.E.10
Piwnica-Worms, H.11
Hibshoosh, H.12
Parsons, R.13
-
7
-
-
33845999615
-
Essential role for nuclear PTEN in maintaining chromosomal integrity
-
Shen WH, Balajee AS, Wang J, Wu H, Eng C, Pandolfi PP, Yin Y. Essential role for nuclear PTEN in maintaining chromosomal integrity. Cell. 2007;128(1):157-170.
-
(2007)
Cell
, vol.128
, Issue.1
, pp. 157-170
-
-
Shen, W.H.1
Balajee, A.S.2
Wang, J.3
Wu, H.4
Eng, C.5
Pandolfi, P.P.6
Yin, Y.7
-
8
-
-
79954613077
-
CREB is a novel nuclear target of PTEN phosphatase
-
Gu T, Zhang Z, Wang J, Guo J, Shen WH, Yin Y. CREB is a novel nuclear target of PTEN phosphatase. Cancer Res. 2011;71(8):2821-2825.
-
(2011)
Cancer Res
, vol.71
, Issue.8
, pp. 2821-2825
-
-
Gu, T.1
Zhang, Z.2
Wang, J.3
Guo, J.4
Shen, W.H.5
Yin, Y.6
-
9
-
-
77954215604
-
The p85beta regulatory subunit of PI3K serves as a substrate for PTEN protein phosphatase activity during insulin mediated signaling
-
He J, de la Monte S, Wands JR. The p85beta regulatory subunit of PI3K serves as a substrate for PTEN protein phosphatase activity during insulin mediated signaling. Biochem Biophys Res Commun. 2010;397(3):513-519.
-
(2010)
Biochem Biophys Res Commun
, vol.397
, Issue.3
, pp. 513-519
-
-
He, J.1
de la Monte, S.2
Wands, J.R.3
-
10
-
-
67649382929
-
AKT-independent signaling downstream of oncogenic PIK3CA mutations in human cancer
-
Vasudevan KM, Barbie DA, Davies MA, Rabinovsky R, McNear CJ, Kim JJ, Hennessy BT, Tseng H, Pochanard P, Kim SY, Dunn IF, Schinzel AC, Sandy P, Hoersch S, Sheng Q, Gupta PB, Boehm JS, Reiling JH, Silver S, Lu Y, Stemke-Hale K, Dutta B, Joy C, Sahin AA, Gonzalez-Angulo AM, Lluch A, Rameh LE, Jacks T, Root DE, Lander ES, Mills GB, Hahn WC, Sellers WR, Garraway LA. AKT-independent signaling downstream of oncogenic PIK3CA mutations in human cancer. Cancer Cell. 2009;16(1):21-32.
-
(2009)
Cancer Cell
, vol.16
, Issue.1
, pp. 21-32
-
-
Vasudevan, K.M.1
Barbie, D.A.2
Davies, M.A.3
Rabinovsky, R.4
McNear, C.J.5
Kim, J.J.6
Hennessy, B.T.7
Tseng, H.8
Pochanard, P.9
Kim, S.Y.10
Dunn, I.F.11
Schinzel, A.C.12
Sandy, P.13
Hoersch, S.14
Sheng, Q.15
Gupta, P.B.16
Boehm, J.S.17
Reiling, J.H.18
Silver, S.19
Lu, Y.20
Stemke-Hale, K.21
Dutta, B.22
Joy, C.23
Sahin, A.A.24
Gonzalez-Angulo, A.M.25
Lluch, A.26
Rameh, L.E.27
Jacks, T.28
Root, D.E.29
Lander, E.S.30
Mills, G.B.31
Hahn, W.C.32
Sellers, W.R.33
Garraway, L.A.34
more..
-
11
-
-
78650877960
-
SGK3 is an estrogen-inducible kinase promoting estrogen-mediated survival of breast cancer cells
-
Wang Y, Zhou D, Phung S, Masri S, Smith D, Chen S. SGK3 is an estrogen-inducible kinase promoting estrogen-mediated survival of breast cancer cells. Mol Endocrinol. 2011;25(1):72-82.
-
(2011)
Mol Endocrinol
, vol.25
, Issue.1
, pp. 72-82
-
-
Wang, Y.1
Zhou, D.2
Phung, S.3
Masri, S.4
Smith, D.5
Chen, S.6
-
12
-
-
78650529080
-
Second AKT: The rise of SGK in cancer signalling
-
Bruhn MA, Pearson RB, Hannan RD, Sheppard KE. Second AKT: the rise of SGK in cancer signalling. Growth Factors. 2010;28(6):394-408.
-
(2010)
Growth Factors
, vol.28
, Issue.6
, pp. 394-408
-
-
Bruhn, M.A.1
Pearson, R.B.2
Hannan, R.D.3
Sheppard, K.E.4
-
13
-
-
0028918408
-
Ras-dependent induction of cellular responses by constitutively active phosphatidylinositol-3 kinase
-
Hu Q, Klippel A, Muslin AJ, Fantl WJ, Williams LT. Ras-dependent induction of cellular responses by constitutively active phosphatidylinositol-3 kinase. Science. 1995;268(5207):100-102.
-
(1995)
Science
, vol.268
, Issue.5207
, pp. 100-102
-
-
Hu, Q.1
Klippel, A.2
Muslin, A.J.3
Fantl, W.J.4
Williams, L.T.5
-
14
-
-
0029943493
-
Phosphatidylinositol 3-kinase is an early intermediate in the G beta gamma-mediated mitogenactivated protein kinase signaling pathway
-
Hawes BE, Luttrell LM, van Biesen T, Lefkowitz RJ. Phosphatidylinositol 3-kinase is an early intermediate in the G beta gamma-mediated mitogenactivated protein kinase signaling pathway. J Biol Chem. 1996;271(21):12133-12136.
-
(1996)
J Biol Chem
, vol.271
, Issue.21
, pp. 12133-12136
-
-
Hawes, B.E.1
Luttrell, L.M.2
van Biesen, T.3
Lefkowitz, R.J.4
-
15
-
-
0033551698
-
Specific contributions of the small GTPases Rho, Rac, and Cdc42 to Dbl transformation
-
Lin R, Cerione RA, Manor D. Specific contributions of the small GTPases Rho, Rac, and Cdc42 to Dbl transformation. J Biol Chem. 1999;274(33): 23633-23641.
-
(1999)
J Biol Chem
, vol.274
, Issue.33
, pp. 23633-23641
-
-
Lin, R.1
Cerione, R.A.2
Manor, D.3
-
16
-
-
0032563936
-
Regulation of protein kinase C zeta by PI 3-kinase and PDK-1
-
Chou MM, Hou W, Johnson J, Graham LK, Lee MH, Chen CS, Newton AC, Schaffhausen BS, Toker A. Regulation of protein kinase C zeta by PI 3-kinase and PDK-1. Curr Biol. 1998;8(19):1069-1077.
-
(1998)
Curr Biol
, vol.8
, Issue.19
, pp. 1069-1077
-
-
Chou, M.M.1
Hou, W.2
Johnson, J.3
Graham, L.K.4
Lee, M.H.5
Chen, C.S.6
Newton, A.C.7
Schaffhausen, B.S.8
Toker, A.9
-
17
-
-
34247116441
-
Physiological roles of PKB/Akt isoforms in development and disease
-
Dummler B, Hemmings BA. Physiological roles of PKB/Akt isoforms in development and disease. Biochem Soc Trans. 2007;35(Pt 2):231-235.
-
(2007)
Biochem Soc Trans
, vol.35
, Issue.Pt 2
, pp. 231-235
-
-
Dummler, B.1
Hemmings, B.A.2
-
19
-
-
80655126355
-
Mtor kinase inhibition causes feedback-dependent biphasic regulation of AKT signaling
-
Rodrik-Outmezguine VS, Chandarlapaty S, Pagano NC, Poulikakos PI, Scaltriti M, Moskatel E, Baselga J, Guichard S, Rosen N. mTOR kinase inhibition causes feedback-dependent biphasic regulation of AKT signaling. Cancer Discov. 2011:1:248-259.
-
(2011)
Cancer Discov
, vol.1
, pp. 248-259
-
-
Rodrik-Outmezguine, V.S.1
Chandarlapaty, S.2
Pagano, N.C.3
Poulikakos, P.I.4
Scaltriti, M.5
Moskatel, E.6
Baselga, J.7
Guichard, S.8
Rosen, N.9
-
20
-
-
0034708482
-
Akt/protein kinase B is regulated by autophosphorylation at the hypothetical PDK-2 site
-
Toker A, Newton AC. Akt/protein kinase B is regulated by autophosphorylation at the hypothetical PDK-2 site. J Biol Chem. 2000;275(12):8271-8274.
-
(2000)
J Biol Chem
, vol.275
, Issue.12
, pp. 8271-8274
-
-
Toker, A.1
Newton, A.C.2
-
21
-
-
0035413599
-
Phosphoinositide- regulated kinases and phosphoinositide phosphatases
-
Leslie NR, Biondi RM, Alessi DR. Phosphoinositide- regulated kinases and phosphoinositide phosphatases. Chem Rev. 2001;101(8):2365-2380.
-
(2001)
Chem Rev
, vol.101
, Issue.8
, pp. 2365-2380
-
-
Leslie, N.R.1
Biondi, R.M.2
Alessi, D.R.3
-
22
-
-
0033594480
-
PDK1 acquires PDK2 activity in the presence of a synthetic peptide derived from the carboxyl terminus of PRK2
-
Balendran A, Casamayor A, Deak M, Paterson A, Gaffney P, Currie R, Downes CP, Alessi DR. PDK1 acquires PDK2 activity in the presence of a synthetic peptide derived from the carboxyl terminus of PRK2. Curr Biol. 1999;9(8):393-404.
-
(1999)
Curr Biol
, vol.9
, Issue.8
, pp. 393-404
-
-
Balendran, A.1
Casamayor, A.2
Deak, M.3
Paterson, A.4
Gaffney, P.5
Currie, R.6
Downes, C.P.7
Alessi, D.R.8
-
23
-
-
13844312400
-
Phosphorylation and regulation of Akt/ PKB by the rictor-mTOR complex
-
Sarbassov DD, Guertin DA, Ali SM, Sabatini DM. Phosphorylation and regulation of Akt/ PKB by the rictor-mTOR complex. Science. 2005;307(5712):1098-1101.
-
(2005)
Science
, vol.307
, Issue.5712
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
Sabatini, D.M.4
-
24
-
-
4644359805
-
Identification of a PKB/Akt hydrophobic motif Ser-473 kinase as DNA-dependent protein kinase
-
Feng J, Park J, Cron P, Hess D, Hemmings BA. Identification of a PKB/Akt hydrophobic motif Ser-473 kinase as DNA-dependent protein kinase. J Biol Chem. 2004;279(39):41189-41196.
-
(2004)
J Biol Chem
, vol.279
, Issue.39
, pp. 41189-41196
-
-
Feng, J.1
Park, J.2
Cron, P.3
Hess, D.4
Hemmings, B.A.5
-
25
-
-
45549104364
-
P53 stabilization in response to DNA damage requires Akt/ PKB and DNA-PK
-
Boehme KA, Kulikov R, Blattner C. p53 stabilization in response to DNA damage requires Akt/ PKB and DNA-PK. Proc Natl Acad Sci U S A. 2008;105(22):7785-7790.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, Issue.22
, pp. 7785-7790
-
-
Boehme, K.A.1
Kulikov, R.2
Blattner, C.3
-
26
-
-
42949165854
-
PKBalpha/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival
-
Bozulic L, Surucu B, Hynx D, Hemmings BA. PKBalpha/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival. Mol Cell. 2008;30(2):203-213.
-
(2008)
Mol Cell
, vol.30
, Issue.2
, pp. 203-213
-
-
Bozulic, L.1
Surucu, B.2
Hynx, D.3
Hemmings, B.A.4
-
27
-
-
0000714961
-
Regulation of protein kinase cascades by protein phosphatase 2A
-
Millward TA, Zolnierowicz S, Hemmings BA. Regulation of protein kinase cascades by protein phosphatase 2A. Trends Biochem Sci. 1999;24(5):186-191.
-
(1999)
Trends Biochem Sci
, vol.24
, Issue.5
, pp. 186-191
-
-
Millward, T.A.1
Zolnierowicz, S.2
Hemmings, B.A.3
-
28
-
-
15944406764
-
PHLPP: A phosphatase that directly dephosphorylates Akt, promotes apoptosis, and suppresses tumor growth
-
Gao T, Furnari F, Newton AC. PHLPP: a phosphatase that directly dephosphorylates Akt, promotes apoptosis, and suppresses tumor growth. Mol Cell. 2005;18(1):13-24.
-
(2005)
Mol Cell
, vol.18
, Issue.1
, pp. 13-24
-
-
Gao, T.1
Furnari, F.2
Newton, A.C.3
-
29
-
-
57649219414
-
In vivo analysis of protein kinase B (PKB)/Akt regulation in DNA-PKcs-null mice reveals a role for PKB/Akt in DNA damage response and tumorigenesis
-
Surucu B, Bozulic L, Hynx D, Parcellier A, Hemmings BA. In vivo analysis of protein kinase B (PKB)/Akt regulation in DNA-PKcs-null mice reveals a role for PKB/Akt in DNA damage response and tumorigenesis. J Biol Chem. 2008;283(44):30025-30033.
-
(2008)
J Biol Chem
, vol.283
, Issue.44
, pp. 30025-30033
-
-
Surucu, B.1
Bozulic, L.2
Hynx, D.3
Parcellier, A.4
Hemmings, B.A.5
-
30
-
-
69249208791
-
The Akt kinases: Isoform specificity in metabolism and cancer
-
Gonzalez E, McGraw TE. The Akt kinases: isoform specificity in metabolism and cancer. Cell Cycle. 2009;8(16):2502-2508.
-
(2009)
Cell Cycle
, vol.8
, Issue.16
, pp. 2502-2508
-
-
Gonzalez, E.1
McGraw, T.E.2
-
31
-
-
84861995114
-
Relative expression levels rather than specific activity plays the major role in determining in vivo AKT isoform substrate specificity
-
2011
-
Lee RS, House CM, Cristiano BE, Hannan RD, Pearson RB, Hannan KM. Relative expression levels rather than specific activity plays the major role in determining in vivo AKT isoform substrate specificity. Enzyme Res. 2011;2011:720985.
-
(2011)
Enzyme Res
, pp. 720985
-
-
Lee, R.S.1
House, C.M.2
Cristiano, B.E.3
Hannan, R.D.4
Pearson, R.B.5
Hannan, K.M.6
-
32
-
-
32044465506
-
TOR signaling in growth and metabolism
-
Wullschleger S, Loewith R, Hall MN. TOR signaling in growth and metabolism. Cell. 2006;124(3):471-484.
-
(2006)
Cell
, vol.124
, Issue.3
, pp. 471-484
-
-
Wullschleger, S.1
Loewith, R.2
Hall, M.N.3
-
33
-
-
33745307617
-
Ras, PI(3)K and mTOR signalling controls tumour cell growth
-
Shaw RJ, Cantley LC. Ras, PI(3)K and mTOR signalling controls tumour cell growth. Nature. 2006;441(7092):424-430.
-
(2006)
Nature
, vol.441
, Issue.7092
, pp. 424-430
-
-
Shaw, R.J.1
Cantley, L.C.2
-
34
-
-
0036713778
-
TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
-
Inoki K, Li Y, Zhu T, Wu J, Guan KL. TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling. Nat Cell Biol. 2002;4(9):648-657.
-
(2002)
Nat Cell Biol
, vol.4
, Issue.9
, pp. 648-657
-
-
Inoki, K.1
Li, Y.2
Zhu, T.3
Wu, J.4
Guan, K.L.5
-
35
-
-
33947264077
-
PRAS40 is an insulin-regulated inhibitor of the mTORC1 protein kinase
-
Sancak Y, Thoreen CC, Peterson TR, Lindquist RA, Kang SA, Spooner E, Carr SA, Sabatini DM. PRAS40 is an insulin-regulated inhibitor of the mTORC1 protein kinase. Mol Cell. 2007;25(6):903-915.
-
(2007)
Mol Cell
, vol.25
, Issue.6
, pp. 903-915
-
-
Sancak, Y.1
Thoreen, C.C.2
Peterson, T.R.3
Lindquist, R.A.4
Kang, S.A.5
Spooner, E.6
Carr, S.A.7
Sabatini, D.M.8
-
36
-
-
0242637318
-
Mtordependent regulation of ribosomal gene transcription requires S6K1 and is mediated by phosphorylation of the carboxy-terminal activation domain of the nucleolar transcription factor UBF
-
Hannan KM, Brandenburger Y, Jenkins A, Sharkey K, Cavanaugh A, Rothblum L, Moss T, Poortinga G, McArthur GA, Pearson RB, Hannan RD. mTORdependent regulation of ribosomal gene transcription requires S6K1 and is mediated by phosphorylation of the carboxy-terminal activation domain of the nucleolar transcription factor UBF. Mol Cell Biol. 2003;23(23):8862-8877.
-
(2003)
Mol Cell Biol
, vol.23
, Issue.23
, pp. 8862-8877
-
-
Hannan, K.M.1
Brandenburger, Y.2
Jenkins, A.3
Sharkey, K.4
Cavanaugh, A.5
Rothblum, L.6
Moss, T.7
Poortinga, G.8
McArthur, G.A.9
Pearson, R.B.10
Hannan, R.D.11
-
37
-
-
33745570504
-
The mTOR/PI3K and MAPK pathways converge on eIF4B to control its phosphorylation and activity
-
Shahbazian D, Roux PP, Mieulet V, Cohen MS, Raught B, Taunton J, Hershey JW, Blenis J, Pende M, Sonenberg N. The mTOR/PI3K and MAPK pathways converge on eIF4B to control its phosphorylation and activity. EMBO J. 2006;25(12):2781-2791.
-
(2006)
EMBO J
, vol.25
, Issue.12
, pp. 2781-2791
-
-
Shahbazian, D.1
Roux, P.P.2
Mieulet, V.3
Cohen, M.S.4
Raught, B.5
Taunton, J.6
Hershey, J.W.7
Blenis, J.8
Pende, M.9
Sonenberg, N.10
-
38
-
-
4644303065
-
SKAR is a specific target of S6 kinase 1 in cell growth control
-
Richardson CJ, Broenstrup M, Fingar DC, Julich K, Ballif BA, Gygi S, Blenis J. SKAR is a specific target of S6 kinase 1 in cell growth control. Curr Biol. 2004;14(17):1540-1549.
-
(2004)
Curr Biol
, vol.14
, Issue.17
, pp. 1540-1549
-
-
Richardson, C.J.1
Broenstrup, M.2
Fingar, D.C.3
Julich, K.4
Ballif, B.A.5
Gygi, S.6
Blenis, J.7
-
39
-
-
80052282364
-
AKT promotes rRNA synthesis and cooperates with c-MYC to stimulate ribosome biogenesis in cancer
-
Chan JC, Hannan KM, Riddell K, Ng PY, Peck A, Lee RS, Hung S, Astle MV, Bywater M, Wall M, Poortinga G, Jastrzebski K, Sheppard KE, Hemmings BA, Hall MN, Johnstone RW, McArthur GA, Hannan RD, Pearson RB. AKT promotes rRNA synthesis and cooperates with c-MYC to stimulate ribosome biogenesis in cancer. Sci Signal. 2011;4(188):ra56.
-
(2011)
Sci Signal
, vol.4
, Issue.188
-
-
Chan, J.C.1
Hannan, K.M.2
Riddell, K.3
Ng, P.Y.4
Peck, A.5
Lee, R.S.6
Hung, S.7
Astle, M.V.8
Bywater, M.9
Wall, M.10
Poortinga, G.11
Jastrzebski, K.12
Sheppard, K.E.13
Hemmings, B.A.14
Hall, M.N.15
Johnstone, R.W.16
McArthur, G.A.17
Hannan, R.D.18
Pearson, R.B.19
-
40
-
-
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(2):214-226.
-
(2008)
Mol Cell
, vol.30
, Issue.2
, 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
-
41
-
-
0345167800
-
TSC2 mediates cellular energy response to control cell growth and survival
-
Inoki K, Zhu T, Guan KL. TSC2 mediates cellular energy response to control cell growth and survival. Cell. 2003;115(5):577-590.
-
(2003)
Cell
, vol.115
, Issue.5
, pp. 577-590
-
-
Inoki, K.1
Zhu, T.2
Guan, K.L.3
-
42
-
-
45849105156
-
The Rag GTPases bind raptor and mediate amino acid signaling to mTORC1
-
Sancak Y, Peterson TR, Shaul YD, Lindquist RA, Thoreen CC, Bar-Peled L, Sabatini DM. The Rag GTPases bind raptor and mediate amino acid signaling to mTORC1. Science. 2008;320(5882):1496-1501.
-
(2008)
Science
, vol.320
, Issue.5882
, pp. 1496-1501
-
-
Sancak, Y.1
Peterson, T.R.2
Shaul, Y.D.3
Lindquist, R.A.4
Thoreen, C.C.5
Bar-Peled, L.6
Sabatini, D.M.7
-
43
-
-
34250788809
-
AKT/PKB signaling: Navigating downstream
-
Manning BD, Cantley LC. AKT/PKB signaling: navigating downstream. Cell. 2007;129(7):1261-1274.
-
(2007)
Cell
, vol.129
, Issue.7
, pp. 1261-1274
-
-
Manning, B.D.1
Cantley, L.C.2
-
44
-
-
0034745353
-
Cytoplasmic localization of p21Cip1/WAF1 by Akt-induced phosphorylation in HER-2/neu-overexpressing cells
-
Zhou BP, Liao Y, Xia W, Spohn B, Lee MH, Hung MC. Cytoplasmic localization of p21Cip1/WAF1 by Akt-induced phosphorylation in HER-2/neu-overexpressing cells. Nat Cell Biol. 2001;3(3):245-252.
-
(2001)
Nat Cell Biol
, vol.3
, Issue.3
, pp. 245-252
-
-
Zhou, B.P.1
Liao, Y.2
Xia, W.3
Spohn, B.4
Lee, M.H.5
Hung, M.C.6
-
45
-
-
0036799377
-
PKB/Akt mediates cellcycle progression by phosphorylation of p27(Kip1) at threonine 157 and modulation of its cellular localization
-
Shin I, Yakes FM, Rojo F, Shin NY, Bakin AV, Baselga J, Arteaga CL. PKB/Akt mediates cellcycle progression by phosphorylation of p27(Kip1) at threonine 157 and modulation of its cellular localization. Nat Med. 2002;8(10):1145-1152.
-
(2002)
Nat Med
, vol.8
, Issue.10
, pp. 1145-1152
-
-
Shin, I.1
Yakes, F.M.2
Rojo, F.3
Shin, N.Y.4
Bakin, A.V.5
Baselga, J.6
Arteaga, C.L.7
-
46
-
-
18644376449
-
PKB/ Akt phosphorylates p27, impairs nuclear import of p27 and opposes p27-mediated G1 arrest
-
Liang J, Zubovitz J, Petrocelli T, Kotchetkov R, Connor MK, Han K, Lee JH, Ciarallo S, Catzavelos C, Beniston R, Franssen E, Slingerland JM. PKB/ Akt phosphorylates p27, impairs nuclear import of p27 and opposes p27-mediated G1 arrest. Nat Med. 2002;8(10):1153-1160.
-
(2002)
Nat Med
, vol.8
, Issue.10
, pp. 1153-1160
-
-
Liang, J.1
Zubovitz, J.2
Petrocelli, T.3
Kotchetkov, R.4
Connor, M.K.5
Han, K.6
Lee, J.H.7
Ciarallo, S.8
Catzavelos, C.9
Beniston, R.10
Franssen, E.11
Slingerland, J.M.12
-
47
-
-
18644370396
-
Cytoplasmic relocalization and inhibition of the cyclin-dependent kinase inhibitor p27(Kip1) by PKB/Akt-mediated phosphorylation in breast cancer
-
Viglietto G, Motti ML, Bruni P, Melillo RM, D'Alessio A, Califano D, Vinci F, Chiappetta G, Tsichlis P, Bellacosa A, Fusco A, Santoro M. Cytoplasmic relocalization and inhibition of the cyclin-dependent kinase inhibitor p27(Kip1) by PKB/Akt-mediated phosphorylation in breast cancer. Nat Med. 2002;8(10):1136-1144.
-
(2002)
Nat Med
, vol.8
, Issue.10
, pp. 1136-1144
-
-
Viglietto, G.1
Motti, M.L.2
Bruni, P.3
Melillo, R.M.4
D'alessio, A.5
Califano, D.6
Vinci, F.7
Chiappetta, G.8
Tsichlis, P.9
Bellacosa, A.10
Fusco, A.11
Santoro, M.12
-
48
-
-
0032533225
-
Glycogen synthase kinase-3beta regulates cyclin D1 proteolysis and subcellular localization
-
Diehl JA, Cheng M, Roussel MF, Sherr CJ. Glycogen synthase kinase-3beta regulates cyclin D1 proteolysis and subcellular localization. Genes Dev. 1998;12(22):3499-3511.
-
(1998)
Genes Dev
, vol.12
, Issue.22
, pp. 3499-3511
-
-
Diehl, J.A.1
Cheng, M.2
Roussel, M.F.3
Sherr, C.J.4
-
49
-
-
0141591688
-
Multisite phosphorylation by Cdk2 and GSK3 controls cyclin E degradation
-
Welcker M, Singer J, Loeb KR, Grim J, Bloecher A, Gurien-West M, Clurman BE, Roberts JM. Multisite phosphorylation by Cdk2 and GSK3 controls cyclin E degradation. Mol Cell. 2003;12(2):381-392.
-
(2003)
Mol Cell
, vol.12
, Issue.2
, pp. 381-392
-
-
Welcker, M.1
Singer, J.2
Loeb, K.R.3
Grim, J.4
Bloecher, A.5
Gurien-West, M.6
Clurman, B.E.7
Roberts, J.M.8
-
50
-
-
22244476115
-
The v-Jun point mutation allows c-Jun to escape GSK3-dependent recognition and destruction by the Fbw7 ubiquitin ligase
-
Wei W, Jin J, Schlisio S, Harper JW, Kaelin WG Jr. The v-Jun point mutation allows c-Jun to escape GSK3-dependent recognition and destruction by the Fbw7 ubiquitin ligase. Cancer Cell. 2005;8(1):25-33.
-
(2005)
Cancer Cell
, vol.8
, Issue.1
, pp. 25-33
-
-
Wei, W.1
Jin, J.2
Schlisio, S.3
Harper, J.W.4
Kaelin Jr., W.G.5
-
51
-
-
2342526543
-
A signalling pathway controlling c-Myc degradation that impacts oncogenic transformation of human cells
-
Yeh E, Cunningham M, Arnold H, Chasse D, Monteith T, Ivaldi G, Hahn WC, Stukenberg PT, Shenolikar S, Uchida T, Counter CM, Nevins JR, Means AR, Sears R. A signalling pathway controlling c-Myc degradation that impacts oncogenic transformation of human cells. Nat Cell Biol. 2004;6(4):308-318.
-
(2004)
Nat Cell Biol
, vol.6
, Issue.4
, pp. 308-318
-
-
Yeh, E.1
Cunningham, M.2
Arnold, H.3
Chasse, D.4
Monteith, T.5
Ivaldi, G.6
Hahn, W.C.7
Stukenberg, P.T.8
Shenolikar, S.9
Uchida, T.10
Counter, C.M.11
Nevins, J.R.12
Means, A.R.13
Sears, R.14
-
52
-
-
0033517190
-
NF-kappaB is a target of AKT in anti-apoptotic PDGF signalling
-
Romashkova JA, Makarov SS. NF-kappaB is a target of AKT in anti-apoptotic PDGF signalling. Nature. 1999;401(6748):86-90.
-
(1999)
Nature
, vol.401
, Issue.6748
, pp. 86-90
-
-
Romashkova, J.A.1
Makarov, S.S.2
-
53
-
-
0033517189
-
NF-kappaB activation by tumour necrosis factor requires the Akt serine-threonine kinase
-
Ozes ON, Mayo LD, Gustin JA, Pfeffer SR, Pfeffer LM, Donner DB. NF-kappaB activation by tumour necrosis factor requires the Akt serine-threonine kinase. Nature. 1999;401(6748):82-85.
-
(1999)
Nature
, vol.401
, Issue.6748
, pp. 82-85
-
-
Ozes, O.N.1
Mayo, L.D.2
Gustin, J.A.3
Pfeffer, S.R.4
Pfeffer, L.M.5
Donner, D.B.6
-
54
-
-
0035133227
-
Akt phosphorylates and negatively regulates apoptosis signal-regulating kinase 1
-
Kim AH, Khursigara G, Sun X, Franke TF, Chao MV. Akt phosphorylates and negatively regulates apoptosis signal-regulating kinase 1. Mol Cell Biol. 2001;21(3):893-901.
-
(2001)
Mol Cell Biol
, vol.21
, Issue.3
, pp. 893-901
-
-
Kim, A.H.1
Khursigara, G.2
Sun, X.3
Franke, T.F.4
Chao, M.V.5
-
55
-
-
0033542414
-
Regulation of endothelium-derived nitric oxide production by the protein kinase Akt
-
Fulton D, Gratton JP, McCabe TJ, Fontana J, Fujio Y, Walsh K, Franke TF, Papapetropoulos A, Sessa WC. Regulation of endothelium-derived nitric oxide production by the protein kinase Akt. Nature. 1999;399(6736):597-601.
-
(1999)
Nature
, vol.399
, Issue.6736
, pp. 597-601
-
-
Fulton, D.1
Gratton, J.P.2
McCabe, T.J.3
Fontana, J.4
Fujio, Y.5
Walsh, K.6
Franke, T.F.7
Papapetropoulos, A.8
Sessa, W.C.9
-
56
-
-
0033542476
-
Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation
-
Dimmeler S, Fleming I, Fisslthaler B, Hermann C, Busse R, Zeiher AM. Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation. Nature. 1999;399(6736):601-605.
-
(1999)
Nature
, vol.399
, Issue.6736
, pp. 601-605
-
-
Dimmeler, S.1
Fleming, I.2
Fisslthaler, B.3
Hermann, C.4
Busse, R.5
Zeiher, A.M.6
-
57
-
-
0037277578
-
Role of nitric oxide in the modulation of angiogenesis
-
Morbidelli L, Donnini S, Ziche M. Role of nitric oxide in the modulation of angiogenesis. Curr Pharm Des. 2003;9(7):521-530.
-
(2003)
Curr Pharm Des
, vol.9
, Issue.7
, pp. 521-530
-
-
Morbidelli, L.1
Donnini, S.2
Ziche, M.3
-
58
-
-
0142166332
-
Targeting HIF-1 for cancer therapy
-
Semenza GL. Targeting HIF-1 for cancer therapy. Nat Rev Cancer. 2003;3(10):721-732.
-
(2003)
Nat Rev Cancer
, vol.3
, Issue.10
, pp. 721-732
-
-
Semenza, G.L.1
-
59
-
-
33846199233
-
Hypoxia-inducible factors: Central regulators of the tumor phenotype
-
Gordan JD, Simon MC. Hypoxia-inducible factors: central regulators of the tumor phenotype. Curr Opin Genet Dev. 2007;17(1):71-77.
-
(2007)
Curr Opin Genet Dev
, vol.17
, Issue.1
, pp. 71-77
-
-
Gordan, J.D.1
Simon, M.C.2
-
60
-
-
67649814136
-
PI3K/PTEN signaling in angiogenesis and tumorigenesis
-
Jiang BH, Liu LZ. PI3K/PTEN signaling in angiogenesis and tumorigenesis. Adv Cancer Res. 2009;102:19-65.
-
(2009)
Adv Cancer Res
, vol.102
, pp. 19-65
-
-
Jiang, B.H.1
Liu, L.Z.2
-
61
-
-
40249116837
-
Regulation of VEGF-mediated angiogenesis by the Akt/PKB substrate Girdin
-
Kitamura T, Asai N, Enomoto A, Maeda K, Kato T, Ishida M, Jiang P, Watanabe T, Usukura J, Kondo T, Costantini F, Murohara T, Takahashi M. Regulation of VEGF-mediated angiogenesis by the Akt/PKB substrate Girdin. Nat Cell Biol. 2008;10(3):329-337.
-
(2008)
Nat Cell Biol
, vol.10
, Issue.3
, pp. 329-337
-
-
Kitamura, T.1
Asai, N.2
Enomoto, A.3
Maeda, K.4
Kato, T.5
Ishida, M.6
Jiang, P.7
Watanabe, T.8
Usukura, J.9
Kondo, T.10
Costantini, F.11
Murohara, T.12
Takahashi, M.13
-
62
-
-
4544343980
-
Inappropriate activation of the TSC/Rheb/mTOR/S6K cassette induces IRS1/2 depletion, insulin resistance, and cell survival deficiencies
-
Shah OJ, Wang Z, Hunter T. Inappropriate activation of the TSC/Rheb/mTOR/S6K cassette induces IRS1/2 depletion, insulin resistance, and cell survival deficiencies. Curr Biol. 2004;14(18):1650-1656.
-
(2004)
Curr Biol
, vol.14
, Issue.18
, pp. 1650-1656
-
-
Shah, O.J.1
Wang, Z.2
Hunter, T.3
-
63
-
-
70350545722
-
Characterization of Rictor phosphorylation sites reveals direct regulation of mTOR complex 2 by S6K1
-
Dibble CC, Asara JM, Manning BD. Characterization of Rictor phosphorylation sites reveals direct regulation of mTOR complex 2 by S6K1. Mol Cell Biol. 2009;29(21):5657-5670.
-
(2009)
Mol Cell Biol
, vol.29
, Issue.21
, pp. 5657-5670
-
-
Dibble, C.C.1
Asara, J.M.2
Manning, B.D.3
-
64
-
-
75749105049
-
Mtorc1-activated S6K1 phosphorylates Rictor on threonine 1135 and regulates mTORC2 signaling
-
Julien LA, Carriere A, Moreau J, Roux PP. mTORC1-activated S6K1 phosphorylates Rictor on threonine 1135 and regulates mTORC2 signaling. Mol Cell Biol. 2010;30(4):908-921.
-
(2010)
Mol Cell Biol
, vol.30
, Issue.4
, pp. 908-921
-
-
Julien, L.A.1
Carriere, A.2
Moreau, J.3
Roux, P.P.4
-
65
-
-
27744569843
-
Mtor and S6K1 mediate assembly of the translation preinitiation complex through dynamic protein interchange and ordered phosphorylation events
-
Holz MK, Ballif BA, Gygi SP, Blenis J. mTOR and S6K1 mediate assembly of the translation preinitiation complex through dynamic protein interchange and ordered phosphorylation events. Cell. 2005;123(4):569-580.
-
(2005)
Cell
, vol.123
, Issue.4
, pp. 569-580
-
-
Holz, M.K.1
Ballif, B.A.2
Gygi, S.P.3
Blenis, J.4
-
66
-
-
0034234924
-
A direct linkage between the phosphoinositide 3-kinase-AKT signaling pathway and the mammalian target of rapamycin in mitogen-stimulated and transformed cells
-
Sekulic A, Hudson CC, Homme JL, Yin P, Otterness DM, Karnitz LM, Abraham RT. A direct linkage between the phosphoinositide 3-kinase-AKT signaling pathway and the mammalian target of rapamycin in mitogen-stimulated and transformed cells. Cancer Res. 2000;60(13):3504-3513.
-
(2000)
Cancer Res
, vol.60
, Issue.13
, pp. 3504-3513
-
-
Sekulic, A.1
Hudson, C.C.2
Homme, J.L.3
Yin, P.4
Otterness, D.M.5
Karnitz, L.M.6
Abraham, R.T.7
-
67
-
-
79958696336
-
Phosphoproteomic analysis identifies Grb10 as an mTORC1 substrate that negatively regulates insulin signaling
-
Yu Y, Yoon SO, Poulogiannis G, Yang Q, Ma XM, Villen J, Kubica N, Hoffman GR, Cantley LC, Gygi SP, Blenis J. Phosphoproteomic analysis identifies Grb10 as an mTORC1 substrate that negatively regulates insulin signaling. Science. 2011;332(6035):1322-1326.
-
(2011)
Science
, vol.332
, Issue.6035
, pp. 1322-1326
-
-
Yu, Y.1
Yoon, S.O.2
Poulogiannis, G.3
Yang, Q.4
Ma, X.M.5
Villen, J.6
Kubica, N.7
Hoffman, G.R.8
Cantley, L.C.9
Gygi, S.P.10
Blenis, J.11
-
68
-
-
79958696694
-
The mTORregulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling
-
Hsu PP, Kang SA, Rameseder J, Zhang Y, Ottina KA, Lim D, Peterson TR, Choi Y, Gray NS, Yaffe MB, Marto JA, Sabatini DM. The mTORregulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling. Science. 2011;332(6035):1317-1322.
-
(2011)
Science
, vol.332
, Issue.6035
, pp. 1317-1322
-
-
Hsu, P.P.1
Kang, S.A.2
Rameseder, J.3
Zhang, Y.4
Ottina, K.A.5
Lim, D.6
Peterson, T.R.7
Choi, Y.8
Gray, N.S.9
Yaffe, M.B.10
Marto, J.A.11
Sabatini, D.M.12
-
69
-
-
78651458656
-
AKT inhibition relieves feedback suppression of receptor tyrosine kinase expression and activity
-
Chandarlapaty S, Sawai A, Scaltriti M, Rodrik- Outmezguine V, Grbovic-Huezo O, Serra V, Majumder PK, Baselga J, Rosen N. AKT inhibition relieves feedback suppression of receptor tyrosine kinase expression and activity. Cancer Cell. 2011;19(1):58-71.
-
(2011)
Cancer Cell
, vol.19
, Issue.1
, pp. 58-71
-
-
Chandarlapaty, S.1
Sawai, A.2
Scaltriti, M.3
Rodrik-Outmezguine, V.4
Grbovic-Huezo, O.5
Serra, V.6
Majumder, P.K.7
Baselga, J.8
Rosen, N.9
-
70
-
-
80755132133
-
Kinome siRNA-phosphoproteomic screen identifies networks regulating AKT signaling
-
Lu Y, Muller M, Smith D, Dutta B, Komurov K, Iadevaia S, Ruths D, Tseng JT, Yu S, Yu Q, Nakhleh L, Balazsi G, Donnelly J, Schurdak M, Morgan-Lappe S, Fesik S, Ram PT, Mills GB. Kinome siRNA-phosphoproteomic screen identifies networks regulating AKT signaling. Oncogene. 2011;30:4567-4577.
-
(2011)
Oncogene
, vol.30
, pp. 4567-4577
-
-
Lu, Y.1
Muller, M.2
Smith, D.3
Dutta, B.4
Komurov, K.5
Iadevaia, S.6
Ruths, D.7
Tseng, J.T.8
Yu, S.9
Yu, Q.10
Nakhleh, L.11
Balazsi, G.12
Donnelly, J.13
Schurdak, M.14
Morgan-Lappe, S.15
Fesik, S.16
Ram, P.T.17
Mills, G.B.18
-
71
-
-
0028074316
-
Phosphatidylinositol-3-OH kinase as a direct target of Ras
-
Rodriguez-Viciana P, Warne PH, Dhand R, Vanhaesebroeck B, Gout I, Fry MJ, Waterfield MD, Downward J. Phosphatidylinositol-3-OH kinase as a direct target of Ras. Nature. 1994;370(6490):527-532.
-
(1994)
Nature
, vol.370
, Issue.6490
, pp. 527-532
-
-
Rodriguez-Viciana, P.1
Warne, P.H.2
Dhand, R.3
Vanhaesebroeck, B.4
Gout, I.5
Fry, M.J.6
Waterfield, M.D.7
Downward, J.8
-
72
-
-
0028500187
-
The activation of phosphatidylinositol 3-kinase by Ras
-
Kodaki T, Woscholski R, Hallberg B, Rodriguez- Viciana P, Downward J, Parker PJ. The activation of phosphatidylinositol 3-kinase by Ras. Curr Biol. 1994;4(9):798-806.
-
(1994)
Curr Biol
, vol.4
, Issue.9
, pp. 798-806
-
-
Kodaki, T.1
Woscholski, R.2
Hallberg, B.3
Rodriguez-Viciana, P.4
Downward, J.5
Parker, P.J.6
-
73
-
-
0037046799
-
Activation of phosphoinositide 3-kinase gamma by Ras
-
Suire S, Hawkins P, Stephens L. Activation of phosphoinositide 3-kinase gamma by Ras. Curr Biol. 2002;12(13):1068-1075.
-
(2002)
Curr Biol
, vol.12
, Issue.13
, pp. 1068-1075
-
-
Suire, S.1
Hawkins, P.2
Stephens, L.3
-
74
-
-
14144254701
-
Quantitative phosphorylation profiling of the ERK/p90 ribosomal S6 kinasesignaling cassette and its targets, the tuberous sclerosis tumor suppressors
-
Ballif BA, Roux PP, Gerber SA, MacKeigan JP, Blenis J, Gygi SP. Quantitative phosphorylation profiling of the ERK/p90 ribosomal S6 kinasesignaling cassette and its targets, the tuberous sclerosis tumor suppressors. Proc Natl Acad Sci U S A. 2005;102(3):667-672.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, Issue.3
, pp. 667-672
-
-
Ballif, B.A.1
Roux, P.P.2
Gerber, S.A.3
Mackeigan, J.P.4
Blenis, J.5
Gygi, S.P.6
-
75
-
-
4544384577
-
Tumor-promoting phorbol esters and activated Ras inactivate the tuberous sclerosis tumor suppressor complex via p90 ribosomal S6 kinase
-
Roux PP, Ballif BA, Anjum R, Gygi SP, Blenis J. Tumor-promoting phorbol esters and activated Ras inactivate the tuberous sclerosis tumor suppressor complex via p90 ribosomal S6 kinase. Proc Natl Acad Sci U S A. 2004;101(37):13489-13494.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, Issue.37
, pp. 13489-13494
-
-
Roux, P.P.1
Ballif, B.A.2
Anjum, R.3
Gygi, S.P.4
Blenis, J.5
-
76
-
-
78650943298
-
ERK1/2 phosphorylate Raptor to promote Ras-dependent activation of mTOR complex 1 (mTORC1)
-
Carriere A, Romeo Y, Acosta-Jaquez HA, Moreau J, Bonneil E, Thibault P, Fingar DC, Roux PP. ERK1/2 phosphorylate Raptor to promote Ras-dependent activation of mTOR complex 1 (mTORC1). J Biol Chem. 2011;286(1):567-577.
-
(2011)
J Biol Chem
, vol.286
, Issue.1
, pp. 567-577
-
-
Carriere, A.1
Romeo, Y.2
Acosta-Jaquez, H.A.3
Moreau, J.4
Bonneil, E.5
Thibault, P.6
Fingar, D.C.7
Roux, P.P.8
-
77
-
-
0029918708
-
Functional interactions of phosphatidylinositol 3-kinase with GTPaseactivating protein in 3T3-L1 adipocytes
-
DePaolo D, Reusch JE, Carel K, Bhuripanyo P, Leitner JW, Draznin B. Functional interactions of phosphatidylinositol 3-kinase with GTPaseactivating protein in 3T3-L1 adipocytes. Mol Cell Biol. 1996;16(4):1450-1457.
-
(1996)
Mol Cell Biol
, vol.16
, Issue.4
, pp. 1450-1457
-
-
Depaolo, D.1
Reusch, J.E.2
Carel, K.3
Bhuripanyo, P.4
Leitner, J.W.5
Draznin, B.6
-
78
-
-
0033607784
-
Differentiation stage-specific inhibition of the Raf-MEK-ERK pathway by Akt
-
Rommel C, Clarke BA, Zimmermann S, Nunez L, Rossman R, Reid K, Moelling K, Yancopoulos GD, Glass DJ. Differentiation stage-specific inhibition of the Raf-MEK-ERK pathway by Akt. Science. 1999;286(5445):1738-1741.
-
(1999)
Science
, vol.286
, Issue.5445
, pp. 1738-1741
-
-
Rommel, C.1
Clarke, B.A.2
Zimmermann, S.3
Nunez, L.4
Rossman, R.5
Reid, K.6
Moelling, K.7
Yancopoulos, G.D.8
Glass, D.J.9
-
79
-
-
0033607633
-
Phosphorylation and regulation of Raf by Akt (protein kinase B)
-
Zimmermann S, Moelling K. Phosphorylation and regulation of Raf by Akt (protein kinase B). Science. 1999;286(5445):1741-1744.
-
(1999)
Science
, vol.286
, Issue.5445
, pp. 1741-1744
-
-
Zimmermann, S.1
Moelling, K.2
-
80
-
-
0034282892
-
Negative regulation of the serine/threonine kinase B-Raf by Akt
-
Guan KL, Figueroa C, Brtva TR, Zhu T, Taylor J, Barber TD, Vojtek AB. Negative regulation of the serine/threonine kinase B-Raf by Akt. J Biol Chem. 2000;275(35):27354-27359.
-
(2000)
J Biol Chem
, vol.275
, Issue.35
, pp. 27354-27359
-
-
Guan, K.L.1
Figueroa, C.2
Brtva, T.R.3
Zhu, T.4
Taylor, J.5
Barber, T.D.6
Vojtek, A.B.7
-
81
-
-
0037080956
-
Regulation of Raf-1 activation and signalling by dephosphorylation
-
Dhillon AS, Meikle S, Yazici Z, Eulitz M, Kolch W. Regulation of Raf-1 activation and signalling by dephosphorylation. EMBO J. 2002;21(1-2):64-71.
-
(2002)
EMBO J
, vol.21
, Issue.1-2
, pp. 64-71
-
-
Dhillon, A.S.1
Meikle, S.2
Yazici, Z.3
Eulitz, M.4
Kolch, W.5
-
82
-
-
33646368397
-
Up-regulation of PTEN (phosphatase and tensin homolog deleted on chromosome ten) mediates p38 MAPK stress signal-induced inhibition of insulin signaling. A cross-talk between stress signaling and insulin signaling in resistin-treated human endothelial cells
-
Shen YH, Zhang L, Gan Y, Wang X, Wang J, LeMaire SA, Coselli JS, Wang XL. Up-regulation of PTEN (phosphatase and tensin homolog deleted on chromosome ten) mediates p38 MAPK stress signal-induced inhibition of insulin signaling. A cross-talk between stress signaling and insulin signaling in resistin-treated human endothelial cells. J Biol Chem. 2006;281(12):7727-7736.
-
(2006)
J Biol Chem
, vol.281
, Issue.12
, pp. 7727-7736
-
-
Shen, Y.H.1
Zhang, L.2
Gan, Y.3
Wang, X.4
Wang, J.5
Lemaire, S.A.6
Coselli, J.S.7
Wang, X.L.8
-
83
-
-
11144358645
-
High frequency of mutations of the PIK3CA gene in human cancers
-
Samuels Y, Wang Z, Bardelli A, Silliman N, Ptak J, Szabo S, Yan H, Gazdar A, Powell SM, Riggins GJ, Willson JK, Markowitz S, Kinzler KW, Vogelstein B, Velculescu VE. High frequency of mutations of the PIK3CA gene in human cancers. Science. 2004;304(5670):554.
-
(2004)
Science
, vol.304
, Issue.5670
, pp. 554
-
-
Samuels, Y.1
Wang, Z.2
Bardelli, A.3
Silliman, N.4
Ptak, J.5
Szabo, S.6
Yan, H.7
Gazdar, A.8
Powell, S.M.9
Riggins, G.J.10
Willson, J.K.11
Markowitz, S.12
Kinzler, K.W.13
Vogelstein, B.14
Velculescu, V.E.15
-
84
-
-
32044466838
-
Exploiting the PI3K/AKT pathway for cancer drug discovery
-
Hennessy BT, Smith DL, Ram PT, Lu Y, Mills GB. Exploiting the PI3K/AKT pathway for cancer drug discovery. Nat Rev Drug Discov. 2005;4(12):988-1004.
-
(2005)
Nat Rev Drug Discov
, vol.4
, Issue.12
, pp. 988-1004
-
-
Hennessy, B.T.1
Smith, D.L.2
Ram, P.T.3
Lu, Y.4
Mills, G.B.5
-
85
-
-
36248962105
-
The genomic landscapes of human breast and colorectal cancers
-
Wood LD, Parsons DW, Jones S, Lin J, Sjoblom T, Leary RJ, Shen D, Boca SM, Barber T, Ptak J, Silliman N, Szabo S, Dezso Z, Ustyanksky V, Nikolskaya T, Nikolsky Y, Karchin R, Wilson PA, Kaminker JS, Zhang Z, Croshaw R, Willis J, Dawson D, Shipitsin M, Willson JK, Sukumar S, Polyak K, Park BH, Pethiyagoda CL, Pant PV, Ballinger DG, Sparks AB, Hartigan J, Smith DR, Suh E, Papadopoulos N, Buckhaults P, Markowitz SD, Parmigiani G, Kinzler KW, Velculescu VE, Vogelstein B. The genomic landscapes of human breast and colorectal cancers. Science. 2007;318(5853):1108-1113.
-
(2007)
Science
, vol.318
, Issue.5853
, pp. 1108-1113
-
-
Wood, L.D.1
Parsons, D.W.2
Jones, S.3
Lin, J.4
Sjoblom, T.5
Leary, R.J.6
Shen, D.7
Boca, S.M.8
Barber, T.9
Ptak, J.10
Silliman, N.11
Szabo, S.12
Dezso, Z.13
Ustyanksky, V.14
Nikolskaya, T.15
Nikolsky, Y.16
Karchin, R.17
Wilson, P.A.18
Kaminker, J.S.19
Zhang, Z.20
Croshaw, R.21
Willis, J.22
Dawson, D.23
Shipitsin, M.24
Willson, J.K.25
Sukumar, S.26
Polyak, K.27
Park, B.H.28
Pethiyagoda, C.L.29
Pant, P.V.30
Ballinger, D.G.31
Sparks, A.B.32
Hartigan, J.33
Smith, D.R.34
Suh, E.35
Papadopoulos, N.36
Buckhaults, P.37
Markowitz, S.D.38
Parmigiani, G.39
Kinzler, K.W.40
Velculescu, V.E.41
Vogelstein, B.42
more..
-
86
-
-
52949127312
-
An integrated genomic analysis of human glioblastoma multiforme
-
Parsons DW, Jones S, Zhang X, Lin JC, Leary RJ, Angenendt P, Mankoo P, Carter H, Siu IM, Gallia GL, Olivi A, McLendon R, Rasheed BA, Keir S, Nikolskaya T, Nikolsky Y, Busam DA, Tekleab H, Diaz LA Jr, Hartigan J, Smith DR, Strausberg RL, Marie SK, Shinjo SM, Yan H, Riggins GJ, Bigner DD, Karchin R, Papadopoulos N, Parmigiani G, Vogelstein B, Velculescu VE, Kinzler KW. An integrated genomic analysis of human glioblastoma multiforme. Science. 2008;321(5897):1807-1812.
-
(2008)
Science
, vol.321
, Issue.5897
, pp. 1807-1812
-
-
Parsons, D.W.1
Jones, S.2
Zhang, X.3
Lin, J.C.4
Leary, R.J.5
Angenendt, P.6
Mankoo, P.7
Carter, H.8
Siu, I.M.9
Gallia, G.L.10
Olivi, A.11
McLendon, R.12
Rasheed, B.A.13
Keir, S.14
Nikolskaya, T.15
Nikolsky, Y.16
Busam, D.A.17
Tekleab, H.18
Diaz Jr., L.A.19
Hartigan, J.20
Smith, D.R.21
Strausberg, R.L.22
Marie, S.K.23
Shinjo, S.M.24
Yan, H.25
Riggins, G.J.26
Bigner, D.D.27
Karchin, R.28
Papadopoulos, N.29
Parmigiani, G.30
Vogelstein, B.31
Velculescu, V.E.32
Kinzler, K.W.33
more..
-
87
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature. 2008;455(7216):1061-1068.
-
(2008)
Nature
, vol.455
, Issue.7216
, pp. 1061-1068
-
-
-
88
-
-
79959838081
-
Integrated genomic analyses of ovarian carcinoma
-
Network CGAR
-
Network CGAR. Integrated genomic analyses of ovarian carcinoma. Nature. 2011;474(7353):609-615.
-
(2011)
Nature
, vol.474
, Issue.7353
, pp. 609-615
-
-
-
89
-
-
0036632368
-
The phosphatidylinositol 3-Kinase AKT pathway in human cancer
-
Vivanco I, Sawyers CL. The phosphatidylinositol 3-Kinase AKT pathway in human cancer. Nat Rev Cancer. 2002;2(7):489-501.
-
(2002)
Nat Rev Cancer
, vol.2
, Issue.7
, pp. 489-501
-
-
Vivanco, I.1
Sawyers, C.L.2
-
90
-
-
0037205048
-
The phosphoinositide 3-kinase pathway
-
Cantley LC. The phosphoinositide 3-kinase pathway. Science. 2002;296(5573):1655-1657.
-
(2002)
Science
, vol.296
, Issue.5573
, pp. 1655-1657
-
-
Cantley, L.C.1
-
91
-
-
67749122122
-
Targeting PI3K signalling in cancer: Opportunities, challenges and limitations
-
Engelman JA. Targeting PI3K signalling in cancer: opportunities, challenges and limitations. Nat Rev Cancer. 2009;9(8):550-562.
-
(2009)
Nat Rev Cancer
, vol.9
, Issue.8
, pp. 550-562
-
-
Engelman, J.A.1
-
92
-
-
51849111556
-
PI3K pathway alterations in cancer: Variations on a theme
-
Yuan TL, Cantley LC. PI3K pathway alterations in cancer: variations on a theme. Oncogene. 2008;27(41):5497-5510.
-
(2008)
Oncogene
, vol.27
, Issue.41
, pp. 5497-5510
-
-
Yuan, T.L.1
Cantley, L.C.2
-
93
-
-
68249093818
-
Targeting the phosphoinositide 3-kinase pathway in cancer
-
Liu P, Cheng H, Roberts TM, Zhao JJ. Targeting the phosphoinositide 3-kinase pathway in cancer. Nat Rev Drug Discov. 2009;8(8):627-644.
-
(2009)
Nat Rev Drug Discov
, vol.8
, Issue.8
, pp. 627-644
-
-
Liu, P.1
Cheng, H.2
Roberts, T.M.3
Zhao, J.J.4
-
94
-
-
34547574720
-
A new mutational AKTivation in the PI3K pathway
-
Brugge J, Hung MC, Mills GB. A new mutational AKTivation in the PI3K pathway. Cancer Cell. 2007;12(2):104-107.
-
(2007)
Cancer Cell
, vol.12
, Issue.2
, pp. 104-107
-
-
Brugge, J.1
Hung, M.C.2
Mills, G.B.3
-
95
-
-
0035886016
-
The phosphatidylinositol 3'-kinase p85alpha gene is an oncogene in human ovarian and colon tumors
-
Philp AJ, Campbell IG, Leet C, Vincan E, Rockman SP, Whitehead RH, Thomas RJ, Phillips WA. The phosphatidylinositol 3'-kinase p85alpha gene is an oncogene in human ovarian and colon tumors. Cancer Res. 2001;61(20):7426-7429.
-
(2001)
Cancer Res
, vol.61
, Issue.20
, pp. 7426-7429
-
-
Philp, A.J.1
Campbell, I.G.2
Leet, C.3
Vincan, E.4
Rockman, S.P.5
Whitehead, R.H.6
Thomas, R.J.7
Phillips, W.A.8
-
96
-
-
34547172596
-
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
-
Carpten JD, Faber AL, Horn C, Donoho GP, Briggs SL, Robbins CM, Hostetter G, Boguslawski S, Moses TY, Savage S, Uhlik M, Lin A, Du J, Qian YW, Zeckner DJ, Tucker-Kellogg G, Touchman J, Patel K, Mousses S, Bittner M, Schevitz R, Lai MH, Blanchard KL, Thomas JE. A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature. 2007;448(7152):439-444.
-
(2007)
Nature
, vol.448
, Issue.7152
, pp. 439-444
-
-
Carpten, J.D.1
Faber, A.L.2
Horn, C.3
Donoho, G.P.4
Briggs, S.L.5
Robbins, C.M.6
Hostetter, G.7
Boguslawski, S.8
Moses, T.Y.9
Savage, S.10
Uhlik, M.11
Lin, A.12
Du, J.13
Qian, Y.W.14
Zeckner, D.J.15
Tucker-Kellogg, G.16
Touchman, J.17
Patel, K.18
Mousses, S.19
Bittner, M.20
Schevitz, R.21
Lai, M.H.22
Blanchard, K.L.23
Thomas, J.E.24
more..
-
97
-
-
53849132331
-
A novel AKT3 mutation in melanoma tumours and cell lines
-
Davies MA, Stemke-Hale K, Tellez C, Calderone TL, Deng W, Prieto VG, Lazar AJ, Gershenwald JE, Mills GB. A novel AKT3 mutation in melanoma tumours and cell lines. Br J Cancer. 2008;99(8):1265-1268.
-
(2008)
Br J Cancer
, vol.99
, Issue.8
, pp. 1265-1268
-
-
Davies, M.A.1
Stemke-Hale, K.2
Tellez, C.3
Calderone, T.L.4
Deng, W.5
Prieto, V.G.6
Lazar, A.J.7
Gershenwald, J.E.8
Mills, G.B.9
-
98
-
-
84857417355
-
Feedback upregulation of HER3 (ErbB3) expression and activity attenuates antitumor effect of PI3K inhibitors
-
Chakrabarty A, Sanchez V, Kuba MG, Rinehart C, Arteaga CL. Feedback upregulation of HER3 (ErbB3) expression and activity attenuates antitumor effect of PI3K inhibitors. Proc Natl Acad Sci U S A. 2012;109:2718-2723.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 2718-2723
-
-
Chakrabarty, A.1
Sanchez, V.2
Kuba, M.G.3
Rinehart, C.4
Arteaga, C.L.5
-
99
-
-
79957917078
-
PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer
-
Serra V, Scaltriti M, Prudkin L, Eichhorn PJ, Ibrahim YH, Chandarlapaty S, Markman B, Rodriguez O, Guzman M, Rodriguez S, Gili M, Russillo M, Parra JL, Singh S, Arribas J, Rosen N, Baselga J. PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer. Oncogene. 2011;30(22):2547-2557.
-
(2011)
Oncogene
, vol.30
, Issue.22
, pp. 2547-2557
-
-
Serra, V.1
Scaltriti, M.2
Prudkin, L.3
Eichhorn, P.J.4
Ibrahim, Y.H.5
Chandarlapaty, S.6
Markman, B.7
Rodriguez, O.8
Guzman, M.9
Rodriguez, S.10
Gili, M.11
Russillo, M.12
Parra, J.L.13
Singh, S.14
Arribas, J.15
Rosen, N.16
Baselga, J.17
-
100
-
-
32944457518
-
Mtor inhibition induces upstream receptor tyrosine kinase signaling and activates Akt
-
O'Reilly KE, Rojo F, She QB, Solit D, Mills GB, Smith D, Lane H, Hofmann F, Hicklin DJ, Ludwig DL, Baselga J, Rosen N. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt. Cancer Res. 2006;66(3):1500-1508.
-
(2006)
Cancer Res
, vol.66
, Issue.3
, pp. 1500-1508
-
-
O'Reilly, K.E.1
Rojo, F.2
She, Q.B.3
Solit, D.4
Mills, G.B.5
Smith, D.6
Lane, H.7
Hofmann, F.8
Hicklin, D.J.9
Ludwig, D.L.10
Baselga, J.11
Rosen, N.12
-
101
-
-
51349164790
-
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3Kdependent feedback loop in human cancer
-
Carracedo A, Ma L, Teruya-Feldstein J, Rojo F, Salmena L, Alimonti A, Egia A, Sasaki AT, Thomas G, Kozma SC, Papa A, Nardella C, Cantley LC, Baselga J, Pandolfi PP. Inhibition of mTORC1 leads to MAPK pathway activation through a PI3Kdependent feedback loop in human cancer. J Clin Invest. 2008;118(9):3065-3074.
-
(2008)
J Clin Invest
, vol.118
, Issue.9
, pp. 3065-3074
-
-
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
-
102
-
-
33747819801
-
Mtor and cancer: Insights into a complex relationship
-
Sabatini DM. mTOR and cancer: insights into a complex relationship. Nat Rev Cancer. 2006;6(9):729-734.
-
(2006)
Nat Rev Cancer
, vol.6
, Issue.9
, pp. 729-734
-
-
Sabatini, D.M.1
-
103
-
-
33746637660
-
Current development of mTOR inhibitors as anticancer agents
-
Faivre S, Kroemer G, Raymond E. Current development of mTOR inhibitors as anticancer agents. Nat Rev Drug Discov. 2006;5(8):671-688.
-
(2006)
Nat Rev Drug Discov
, vol.5
, Issue.8
, pp. 671-688
-
-
Faivre, S.1
Kroemer, G.2
Raymond, E.3
-
104
-
-
67650228579
-
Rapamycin inhibits mTORC1, but not completely
-
Thoreen CC, Sabatini DM. Rapamycin inhibits mTORC1, but not completely. Autophagy. 2009;5(5):725-726.
-
(2009)
Autophagy
, vol.5
, Issue.5
, pp. 725-726
-
-
Thoreen, C.C.1
Sabatini, D.M.2
-
105
-
-
0034722888
-
The rapamycin-sensitive signal transduction pathway as a target for cancer therapy
-
Hidalgo M, Rowinsky EK. The rapamycin-sensitive signal transduction pathway as a target for cancer therapy. Oncogene. 2000;19(56):6680-6686.
-
(2000)
Oncogene
, vol.19
, Issue.56
, pp. 6680-6686
-
-
Hidalgo, M.1
Rowinsky, E.K.2
-
106
-
-
16844371494
-
Effects of the mammalian target of rapamycin inhibitor CCI- 779 used alone or with chemotherapy on human prostate cancer cells and xenografts
-
Wu L, Birle DC, Tannock IF. Effects of the mammalian target of rapamycin inhibitor CCI- 779 used alone or with chemotherapy on human prostate cancer cells and xenografts. Cancer Res. 2005;65(7):2825-2831.
-
(2005)
Cancer Res
, vol.65
, Issue.7
, pp. 2825-2831
-
-
Wu, L.1
Birle, D.C.2
Tannock, I.F.3
-
107
-
-
84863078767
-
Everolimus in postmenopausal hormone-receptor- positive advanced breast cancer
-
Baselga J, Campone M, Piccart M, Burris HA, Rugo HS, Sahmoud T, Noguchi S, Gnant M, Pritchard KI, Lebrun F, Beck JT, Ito Y, Yardley D, Deleu I, Perez A, Bachelot T, Vittori L, Xu Z, Mukhopadhyay P, Lebwohl D, Hortobagyi GN. Everolimus in postmenopausal hormone-receptor- positive advanced breast cancer. N Engl J Med. 2012;366:520-529.
-
(2012)
N Engl J Med
, vol.366
, pp. 520-529
-
-
Baselga, J.1
Campone, M.2
Piccart, M.3
Burris, H.A.4
Rugo, H.S.5
Sahmoud, T.6
Noguchi, S.7
Gnant, M.8
Pritchard, K.I.9
Lebrun, F.10
Beck, J.T.11
Ito, Y.12
Yardley, D.13
Deleu, I.14
Perez, A.15
Bachelot, T.16
Vittori, L.17
Xu, Z.18
Mukhopadhyay, P.19
Lebwohl, D.20
Hortobagyi, G.N.21
more..
-
108
-
-
48649107474
-
Efficacy of everolimus in advanced renal cell carcinoma: A double-blind, randomised, placebo-controlled phase III trial
-
Motzer RJ, Escudier B, Oudard S, Hutson TE, Porta C, Bracarda S, Grunwald V, Thompson JA, Figlin RA, Hollaender N, Urbanowitz G, Berg WJ, Kay A, Lebwohl D, Ravaud A. Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial. Lancet. 2008;372(9637):449-456.
-
(2008)
Lancet
, vol.372
, Issue.9637
, pp. 449-456
-
-
Motzer, R.J.1
Escudier, B.2
Oudard, S.3
Hutson, T.E.4
Porta, C.5
Bracarda, S.6
Grunwald, V.7
Thompson, J.A.8
Figlin, R.A.9
Hollaender, N.10
Urbanowitz, G.11
Berg, W.J.12
Kay, A.13
Lebwohl, D.14
Ravaud, A.15
-
109
-
-
77956227464
-
Phase 3 trial of everolimus for metastatic renal cell carcinoma: Final results and analysis of prognostic factors
-
Motzer RJ, Escudier B, Oudard S, Hutson TE, Porta C, Bracarda S, Grunwald V, Thompson JA, Figlin RA, Hollaender N, Kay A, Ravaud A. Phase 3 trial of everolimus for metastatic renal cell carcinoma: final results and analysis of prognostic factors. Cancer. 2010;116(18):4256-4265.
-
(2010)
Cancer
, vol.116
, Issue.18
, pp. 4256-4265
-
-
Motzer, R.J.1
Escudier, B.2
Oudard, S.3
Hutson, T.E.4
Porta, C.5
Bracarda, S.6
Grunwald, V.7
Thompson, J.A.8
Figlin, R.A.9
Hollaender, N.10
Kay, A.11
Ravaud, A.12
-
110
-
-
34249779568
-
Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma
-
Hudes G, Carducci M, Tomczak P, Dutcher J, Figlin R, Kapoor A, Staroslawska E, Sosman J, McDermott D, Bodrogi I, Kovacevic Z, Lesovoy V, Schmidt-Wolf IG, Barbarash O, Gokmen E, O'Toole T, Lustgarten S, Moore L, Motzer RJ. Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. N Engl J Med. 2007;356(22):2271-2281.
-
(2007)
N Engl J Med
, vol.356
, Issue.22
, pp. 2271-2281
-
-
Hudes, G.1
Carducci, M.2
Tomczak, P.3
Dutcher, J.4
Figlin, R.5
Kapoor, A.6
Staroslawska, E.7
Sosman, J.8
McDermott, D.9
Bodrogi, I.10
Kovacevic, Z.11
Lesovoy, V.12
Schmidt-Wolf, I.G.13
Barbarash, O.14
Gokmen, E.15
O'Toole, T.16
Lustgarten, S.17
Moore, L.18
Motzer, R.J.19
-
111
-
-
79851500081
-
Everolimus for advanced pancreatic neuroendocrine tumors
-
Yao JC, Shah MH, Ito T, Bohas CL, Wolin EM, Van Cutsem E, Hobday TJ, Okusaka T, Capdevila J, de Vries EG, Tomassetti P, Pavel ME, Hoosen S, Haas T, Lincy J, Lebwohl D, Oberg K. Everolimus for advanced pancreatic neuroendocrine tumors. N Engl J Med. 2011;364(6):514-523.
-
(2011)
N Engl J Med
, vol.364
, Issue.6
, pp. 514-523
-
-
Yao, J.C.1
Shah, M.H.2
Ito, T.3
Bohas, C.L.4
Wolin, E.M.5
van Cutsem, E.6
Hobday, T.J.7
Okusaka, T.8
Capdevila, J.9
de Vries, E.G.10
Tomassetti, P.11
Pavel, M.E.12
Hoosen, S.13
Haas, T.14
Lincy, J.15
Lebwohl, D.16
Oberg, K.17
-
112
-
-
78049510428
-
Everolimus for subependymal giant-cell astrocytomas in tuberous sclerosis
-
Krueger DA, Care MM, Holland K, Agricola K, Tudor C, Mangeshkar P, Wilson KA, Byars A, Sahmoud T, Franz DN. Everolimus for subependymal giant-cell astrocytomas in tuberous sclerosis. N Engl J Med. 2010;363(19):1801-1811.
-
(2010)
N Engl J Med
, vol.363
, Issue.19
, pp. 1801-1811
-
-
Krueger, D.A.1
Care, M.M.2
Holland, K.3
Agricola, K.4
Tudor, C.5
Mangeshkar, P.6
Wilson, K.A.7
Byars, A.8
Sahmoud, T.9
Franz, D.N.10
-
113
-
-
79954524112
-
Mechanism of cell adaptation: When and how do cancer cells develop chemoresistance?
-
Fodale V, Pierobon M, Liotta L, Petricoin E. Mechanism of cell adaptation: when and how do cancer cells develop chemoresistance? Cancer J. 2011;17(2):89-95.
-
(2011)
Cancer J
, vol.17
, Issue.2
, pp. 89-95
-
-
Fodale, V.1
Pierobon, M.2
Liotta, L.3
Petricoin, E.4
-
114
-
-
38849208347
-
Antitumor activity of rapamycin in a Phase I trial for patients with recurrent PTENdeficient glioblastoma
-
Cloughesy TF, Yoshimoto K, Nghiemphu P, Brown K, Dang J, Zhu S, Hsueh T, Chen Y, Wang W, Youngkin D, Liau L, Martin N, Becker D, Bergsneider M, Lai A, Green R, Oglesby T, Koleto M, Trent J, Horvath S, Mischel PS, Mellinghoff IK, Sawyers CL. Antitumor activity of rapamycin in a Phase I trial for patients with recurrent PTENdeficient glioblastoma. PLoS Med. 2008;5(1):e8.
-
(2008)
PLoS Med
, vol.5
, Issue.1
-
-
Cloughesy, T.F.1
Yoshimoto, K.2
Nghiemphu, P.3
Brown, K.4
Dang, J.5
Zhu, S.6
Hsueh, T.7
Chen, Y.8
Wang, W.9
Youngkin, D.10
Liau, L.11
Martin, N.12
Becker, D.13
Bergsneider, M.14
Lai, A.15
Green, R.16
Oglesby, T.17
Koleto, M.18
Trent, J.19
Horvath, S.20
Mischel, P.S.21
Mellinghoff, I.K.22
Sawyers, C.L.23
more..
-
115
-
-
23844438209
-
Activation of Akt and eIF4E survival pathways by rapamycin-mediated mammalian target of rapamycin inhibition
-
Sun SY, Rosenberg LM, Wang X, Zhou Z, Yue P, Fu H, Khuri FR. Activation of Akt and eIF4E survival pathways by rapamycin-mediated mammalian target of rapamycin inhibition. Cancer Res. 2005;65(16):7052-7058.
-
(2005)
Cancer Res
, vol.65
, Issue.16
, pp. 7052-7058
-
-
Sun, S.Y.1
Rosenberg, L.M.2
Wang, X.3
Zhou, Z.4
Yue, P.5
Fu, H.6
Khuri, F.R.7
-
116
-
-
27644534999
-
Mammalian target of rapamycin inhibitors activate the AKT kinase in multiple myeloma cells by up-regulating the insulin-like growth factor receptor/insulin receptor substrate-1/phosphatidylinositol 3-kinase cascade
-
Shi Y, Yan H, Frost P, Gera J, Lichtenstein A. Mammalian target of rapamycin inhibitors activate the AKT kinase in multiple myeloma cells by up-regulating the insulin-like growth factor receptor/insulin receptor substrate-1/phosphatidylinositol 3-kinase cascade. Mol Cancer Ther. 2005;4(10):1533-1540.
-
(2005)
Mol Cancer Ther
, vol.4
, Issue.10
, pp. 1533-1540
-
-
Shi, Y.1
Yan, H.2
Frost, P.3
Gera, J.4
Lichtenstein, A.5
-
117
-
-
65549145048
-
An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1
-
Thoreen CC, Kang SA, Chang JW, Liu Q, Zhang J, Gao Y, Reichling LJ, Sim T, Sabatini DM, Gray NS. An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1. J Biol Chem. 2009;284(12):8023-8032.
-
(2009)
J Biol Chem
, vol.284
, Issue.12
, pp. 8023-8032
-
-
Thoreen, C.C.1
Kang, S.A.2
Chang, J.W.3
Liu, Q.4
Zhang, J.5
Gao, Y.6
Reichling, L.J.7
Sim, T.8
Sabatini, D.M.9
Gray, N.S.10
-
118
-
-
61349141302
-
Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2
-
Feldman ME, Apsel B, Uotila A, Loewith R, Knight ZA, Ruggero D, Shokat KM. Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2. PLoS Biol. 2009;7(2):e38.
-
(2009)
PLoS Biol
, vol.7
, Issue.2
-
-
Feldman, M.E.1
Apsel, B.2
Uotila, A.3
Loewith, R.4
Knight, Z.A.5
Ruggero, D.6
Shokat, K.M.7
-
119
-
-
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
-
Suppl; Abstr 3006
-
Tan DS, Dumez H, Olmos D, Sandhu SK, Hoeben A, Stephens AW, Poondru S, Gedrich R, Kaye SB, Schoffsk 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 Oncol. 2010;28:15s(Suppl; Abstr 3006).
-
(2010)
J Clin Oncol
, vol.28
-
-
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
Schoffsk, P.10
-
120
-
-
51449095342
-
Targeting the PI3K-AKTmTOR pathway: Progress, pitfalls, and promises
-
Aug
-
Yap TA, Garrett MD, Walton MI, Raynaud F, de Bono JS, Workman P. Targeting the PI3K-AKTmTOR pathway: progress, pitfalls, and promises. Curr Opin Pharmacol. 2008 Aug;8(4):393-412.
-
(2008)
Curr Opin Pharmacol
, vol.8
, Issue.4
, pp. 393-412
-
-
Yap, T.A.1
Garrett, M.D.2
Walton, M.I.3
Raynaud, F.4
de Bono, J.S.5
Workman, P.6
-
121
-
-
77954746352
-
The efficacy of the novel dual PI3-kinase/mTOR inhibitor NVP-BEZ235 compared with rapamycin in renal cell carcinoma
-
Jul 15
-
Cho DC, Cohen MB, Panka DJ, Collins M, Ghebremichael M, Atkins MB, Signoretti S, Mier JW. The efficacy of the novel dual PI3-kinase/mTOR inhibitor NVP-BEZ235 compared with rapamycin in renal cell carcinoma. Clin Cancer Res. 2010 Jul 15;16(14):3628-3638.
-
(2010)
Clin Cancer Res
, vol.16
, Issue.14
, pp. 3628-3638
-
-
Cho, D.C.1
Cohen, M.B.2
Panka, D.J.3
Collins, M.4
Ghebremichael, M.5
Atkins, M.B.6
Signoretti, S.7
Mier, J.W.8
-
122
-
-
65549142212
-
Targeting melanoma with dual phosphoinositide 3-kinase/mammalian target of rapamycin inhibitors
-
Apr
-
Marone R, Erhart D, Mertz AC, Bohnacker T, Schnell C, Cmiljanovic V, Stauffer F, Garcia- Echeverria C, Giese B, Maira SM, Wymann MP. Targeting melanoma with dual phosphoinositide 3-kinase/mammalian target of rapamycin inhibitors. Mol Cancer Res. 2009 Apr;7(4):601-613.
-
(2009)
Mol Cancer Res
, vol.7
, Issue.4
, pp. 601-613
-
-
Marone, R.1
Erhart, D.2
Mertz, A.C.3
Bohnacker, T.4
Schnell, C.5
Cmiljanovic, V.6
Stauffer, F.7
Garcia-Echeverria, C.8
Giese, B.9
Maira, S.M.10
Wymann, M.P.11
-
123
-
-
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
-
Jul
-
Maira SM, Stauffer F, Brueggen J, Furet P, Schnell C, Fritsch C, Brachmann S, Chene P, De Pover A, Schoemaker K, Fabbro D, Gabriel D, Simonen M, Murphy L, Finan P, Sellers W, Garcia-Echeverria C. 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 Jul;7(7):1851-1863.
-
(2008)
Mol Cancer Ther
, vol.7
, Issue.7
, pp. 1851-1863
-
-
Maira, S.M.1
Stauffer, F.2
Brueggen, J.3
Furet, P.4
Schnell, C.5
Fritsch, 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
Garcia-Echeverria, C.17
-
124
-
-
51849111524
-
NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations
-
Oct 1
-
Serra V, Markman B, Scaltriti M, Eichhorn PJA, Valero V, Guzman M, Botero ML, Llonch E, Atzori F, Di Cosimo S, Maira M, Garcia-Echeverria C, Parra JL, Arribas J, Baselga J. NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations. Cancer research. 2008 Oct 1;68(19):8022-8030.
-
(2008)
Cancer Research
, vol.68
, Issue.19
, pp. 8022-8030
-
-
Serra, V.1
Markman, B.2
Scaltriti, M.3
Eichhorn, P.J.A.4
Valero, V.5
Guzman, M.6
Botero, M.L.7
Llonch, E.8
Atzori, F.9
di Cosimo, S.10
Maira, M.11
Garcia-Echeverria, C.12
Parra, J.L.13
Arribas, J.14
Baselga, J.15
-
125
-
-
53049087363
-
Effects of the dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor NVP-BEZ235 on the tumor vasculature: Implications for clinical imaging
-
Aug 15
-
Schnell CR, Stauffer F, Allegrini PR, O'Reilly T, McSheehy PM, Dartois C, Stumm M, Cozens R, Littlewood-Evans A, Garcia-Echeverria C, Maira SM. Effects of the dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor NVP-BEZ235 on the tumor vasculature: implications for clinical imaging. Cancer Res. 2008 Aug 15;68(16):6598-6607.
-
(2008)
Cancer Res
, vol.68
, Issue.16
, pp. 6598-6607
-
-
Schnell, C.R.1
Stauffer, F.2
Allegrini, P.R.3
O'Reilly, T.4
McSheehy, P.M.5
Dartois, C.6
Stumm, M.7
Cozens, R.8
Littlewood-Evans, A.9
Garcia-Echeverria, C.10
Maira, S.M.11
-
126
-
-
80051584382
-
In Vivo Activity of Combined PI3K/ mTOR and MEK Inhibition in a KrasG12D;Pten Deletion Mouse Model of Ovarian Cancer
-
Aug
-
Kinross KM, Brown DV, Kleinschmidt M, Jackson S, Christensen J, Cullinane C, Hicks RJ, Johnstone RW, McArthur GA. In Vivo Activity of Combined PI3K/ mTOR and MEK Inhibition in a KrasG12D;Pten Deletion Mouse Model of Ovarian Cancer. Mol Cancer Ther. 2011 Aug;10(8):1440-1449.
-
(2011)
Mol Cancer Ther
, vol.10
, Issue.8
, pp. 1440-1449
-
-
Kinross, K.M.1
Brown, D.V.2
Kleinschmidt, M.3
Jackson, S.4
Christensen, J.5
Cullinane, C.6
Hicks, R.J.7
Johnstone, R.W.8
McArthur, G.A.9
-
127
-
-
81055149891
-
PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity
-
Jul 12
-
Yuan J, Mehta PP, Yin M-J, 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, McHarg A, Cheng H, Christensen JG, Kan JLC, Bagrodia S. PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity. Mol Cancer Ther. 2011 Jul 12.
-
(2011)
Mol Cancer Ther
-
-
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
McHarg, A.17
Cheng, H.18
Christensen, J.G.19
Kan, J.L.C.20
Bagrodia, S.21
more..
-
128
-
-
57349194139
-
Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
-
Dec
-
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, Garcia-Echeverria C, Weissleder R, Mahmood U, Cantley LC, Wong KK. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat Med. 2008 Dec;14(12):1351-1356.
-
(2008)
Nat Med
, vol.14
, Issue.12
, 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
Garcia-Echeverria, C.17
Weissleder, R.18
Mahmood, U.19
Cantley, L.C.20
Wong, K.K.21
more..
-
129
-
-
51349100763
-
A chemical screen in diverse breast cancer cell lines reveals genetic enhancers and suppressors of sensitivity to PI3K isoform-selective inhibition
-
Oct 1
-
Torbett NE, Luna-Moran A, Knight ZA, Houk A, Moasser M, Weiss W, Shokat KM, Stokoe D. A chemical screen in diverse breast cancer cell lines reveals genetic enhancers and suppressors of sensitivity to PI3K isoform-selective inhibition. Biochem J. 2008 Oct 1;415(1):97-110.
-
(2008)
Biochem J
, vol.415
, Issue.1
, pp. 97-110
-
-
Torbett, N.E.1
Luna-Moran, A.2
Knight, Z.A.3
Houk, A.4
Moasser, M.5
Weiss, W.6
Shokat, K.M.7
Stokoe, D.8
-
130
-
-
58249120506
-
Mutations in the phosphatidylinositol- 3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance
-
Jan 1
-
Ihle NT, Lemos R, Jr., Wipf P, Yacoub A, Mitchell C, Siwak D, Mills GB, Dent P, Kirkpatrick DL, Powis G. Mutations in the phosphatidylinositol- 3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance. Cancer Res. 2009 Jan 1;69(1):143-150.
-
(2009)
Cancer Res
, vol.69
, Issue.1
, pp. 143-150
-
-
Ihle, N.T.1
Lemos Jr., R.2
Wipf, P.3
Yacoub, A.4
Mitchell, C.5
Siwak, D.6
Mills, G.B.7
Dent, P.8
Kirkpatrick, D.L.9
Powis, G.10
-
131
-
-
80054751392
-
Phase I study of the multikinase prodrug SF1126 in solid tumors and B-cell malignancies
-
Suppl; Abstr 3015
-
Mahadevan D, Chiorean EG, Harris W, Von Hoff DD, Younger A, Rensvold DM, Cordova F, Qi W, Shelton CF, Becker MD, Garlich JR, Ramanathan RK. Phase I study of the multikinase prodrug SF1126 in solid tumors and B-cell malignancies. J Clin Oncol 29. 2011;29(Suppl; Abstr 3015).
-
(2011)
J Clin Oncol
, vol.29
, pp. 29
-
-
Mahadevan, D.1
Chiorean, E.G.2
Harris, W.3
von Hoff, D.D.4
Younger, A.5
Rensvold, D.M.6
Cordova, F.7
Qi, W.8
Shelton, C.F.9
Becker, M.D.10
Garlich, J.R.11
Ramanathan, R.K.12
-
132
-
-
77957104533
-
A phase I dose-escalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765 (SAR245409), a PI3K/ TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced malignancies
-
(Suppl; Abstr 3030)
-
Brana I, P. LoRusso P. J. Baselga J. E. I. Heath EI, A. Patnaik A. S. Gendreau S.A. Laird A. K. Papadopoulos K. A phase I dose-escalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765 (SAR245409), a PI3K/ TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced malignancies. J Clin Oncol. 2010;28:15s(Suppl; Abstr 3030).
-
(2010)
J Clin Oncol
, vol.15 s
, pp. 28
-
-
Brana, I.1
Lorusso, P.2
Baselga, J.E.I.3
Heath, P.J.4
Patnaik, E.A.5
Gendreau, A.S.6
Papadopoulos, S.A.7
Laird, A.K.8
-
133
-
-
77956602070
-
First-in-human phase I study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors
-
(Suppl; Abstr 3005)
-
Burris H, Rodon J, Sharma S, Herbst RS, Tabernero J, Infante JR, Silva A, Demanse D, Hackl W, Baselga J. First-in-human phase I study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors. J Clin Oncol 2010;28:15s(Suppl; Abstr 3005).
-
(2010)
J Clin Oncol
, vol.28
-
-
Burris, H.1
Rodon, J.2
Sharma, S.3
Herbst, R.S.4
Tabernero, J.5
Infante, J.R.6
Silva, A.7
Demanse, D.8
Hackl, W.9
Baselga, J.10
-
134
-
-
84856988295
-
A dose-escalation study with the novel formulation of the oral pan-class I PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors
-
(Suppl; Abstr 3066)
-
Peyton JD, Rodon Ahnert J, Burris H, Britten C, Chen LC, Tabernero J, Duval V, Rouyrre N, Silva AP, Quadt C, Baselga J. A dose-escalation study with the novel formulation of the oral pan-class I PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors. J Clin Oncol 2011;29. (Suppl; Abstr 3066).
-
(2011)
J Clin Oncol
, pp. 29
-
-
Peyton, J.D.1
Rodon, A.J.2
Burris, H.3
Britten, C.4
Chen, L.C.5
Tabernero, J.6
Duval, V.7
Rouyrre, N.8
Silva, A.P.9
Quadt, C.10
Baselga, J.11
-
135
-
-
80054740282
-
A first-in-human phase I study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors
-
(Suppl; Abstr 3020)
-
Wagner AJ, Bendell JC, Dolly S, Morgan JA, Ware JA, Fredrickson J, Mazina KE, Lauchle JO, Burris HA, De Bono JS. A first-in-human phase I study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors. J Clin Oncol. 2011;29. (Suppl; Abstr 3020).
-
(2011)
J Clin Oncol
, pp. 29
-
-
Wagner, A.J.1
Bendell, J.C.2
Dolly, S.3
Morgan, J.A.4
Ware, J.A.5
Fredrickson, J.6
Mazina, K.E.7
Lauchle, J.O.8
Burris, H.A.9
de Bono, J.S.10
-
136
-
-
80054748915
-
Phase I first-in-human study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826)
-
(Suppl; Abstr 3018)
-
Munster N, van der Noll R, Voest EE, Dees EC, Tan AR, Specht JM, Falchook GS, Daud A, Lolkema MP, Grilley-Olson JE, Yu EY, Fu S, Bergsland EK, Kleha J, Peng S, Smith DA, Lampkin TA, Schellens JHM, Morris SR, Kurzrock R. Phase I first-in-human study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826). J Clin Oncol. 2011;29. (Suppl; Abstr 3018).
-
(2011)
J Clin Oncol
, pp. 29
-
-
Munster, N.1
van der Noll, R.2
Voest, E.E.3
Dees, E.C.4
Tan, A.R.5
Specht, J.M.6
Falchook, G.S.7
Daud, A.8
Lolkema, M.P.9
Grilley-Olson, J.E.10
Yu, E.Y.11
Fu, S.12
Bergsland, E.K.13
Kleha, J.14
Peng, S.15
Smith, D.A.16
Lampkin, T.A.17
Schellens, J.H.M.18
Morris, S.R.19
Kurzrock, R.20
more..
-
137
-
-
67649386846
-
The antiproliferative cytostatic effects of a self-activating viridin prodrug
-
Jun
-
Smith A, Blois J, Yuan H, Aikawa E, Ellson C, Figueiredo JL, Weissleder R, Kohler R, Yaffe MB, Cantley LC, Josephson L. The antiproliferative cytostatic effects of a self-activating viridin prodrug. Mol Cancer Ther. 2009 Jun;8(6):1666-1675.
-
(2009)
Mol Cancer Ther
, vol.8
, Issue.6
, pp. 1666-1675
-
-
Smith, A.1
Blois, J.2
Yuan, H.3
Aikawa, E.4
Ellson, C.5
Figueiredo, J.L.6
Weissleder, R.7
Kohler, R.8
Yaffe, M.B.9
Cantley, L.C.10
Josephson, L.11
-
138
-
-
84860390340
-
Preclinical modeling of combined phosphatidylinositol-3-kinase inhibition with endocrine therapy for estrogen receptor-positive breast cancer
-
Mar 1
-
Sanchez CG, Ma CX, Crowder RJ, Guintoli T, Phommaly C, Gao F, Lin L, Ellis MJ. Preclinical modeling of combined phosphatidylinositol-3-kinase inhibition with endocrine therapy for estrogen receptor-positive breast cancer. Breast Cancer Res. 2011 Mar 1;13(2):R21.
-
(2011)
Breast Cancer Res
, vol.13
, Issue.2
-
-
Sanchez, C.G.1
Ma, C.X.2
Crowder, R.J.3
Guintoli, T.4
Phommaly, C.5
Gao, F.6
Lin, L.7
Ellis, M.J.8
-
139
-
-
34748840281
-
The phosphatidylinositol 3-kinase inhibitor, PX-866, is a potent inhibitor of cancer cell motility and growth in three-dimensional cultures
-
Sep
-
Howes AL, Chiang GG, Lang ES, Ho CB, Powis G, Vuori K, Abraham RT. The phosphatidylinositol 3-kinase inhibitor, PX-866, is a potent inhibitor of cancer cell motility and growth in three-dimensional cultures. Mol Cancer Ther. 2007 Sep;6(9): 2505-2514.
-
(2007)
Mol Cancer Ther
, vol.6
, Issue.9
, pp. 2505-2514
-
-
Howes, A.L.1
Chiang, G.G.2
Lang, E.S.3
Ho, C.B.4
Powis, G.5
Vuori, K.6
Abraham, R.T.7
-
140
-
-
84859386094
-
Oral PI3 kinase inhibitor BKM120 monotherapy in patients (pts) with advanced solid tumors: An update on safety and efficacy
-
(Suppl; Abstr 3043)
-
Grana B, Burris HA, Rodon Ahnert J, Abdul Razak AR, De Jonge MJ, Eskens F, Siu LL, Ru QC, Homji NF, Demanse D, Di Tomaso E, Cosaert JGCE, Quadt C, Baselga J, Bendell JC. Oral PI3 kinase inhibitor BKM120 monotherapy in patients (pts) with advanced solid tumors: An update on safety and efficacy. J Clin Oncol. 2011;29. (Suppl; Abstr 3043).
-
(2011)
J Clin Oncol
, pp. 29
-
-
Grana, B.1
Burris, H.A.2
Rodon, A.J.3
Abdul, R.A.R.4
de Jonge, M.J.5
Eskens, F.6
Siu, L.L.7
Ru, Q.C.8
Homji, N.F.9
Demanse, D.10
di Tomaso, E.11
Cosaert, J.G.C.E.12
Quadt, C.13
Baselga, J.14
Bendell, J.C.15
-
141
-
-
84861963385
-
A phase I dose-escalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors
-
(Suppl; Abstr 3052)
-
Von Hoff DD, LoRusso P, Demetri GD, Weiss GJ, Shapiro G, Ramanathan RK, Ware JA, Raja R, Jin J, Levy GG, Mazina KE, Wagner AJ. A phase I dose-escalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors. J Clin Oncol. 2011;29. (Suppl; Abstr 3052).
-
(2011)
J Clin Oncol
, pp. 29
-
-
von Hoff, D.D.1
Lorusso, P.2
Demetri, G.D.3
Weiss, G.J.4
Shapiro, G.5
Ramanathan, R.K.6
Ware, J.A.7
Raja, R.8
Jin, J.9
Levy, G.G.10
Mazina, K.E.11
Wagner, A.J.12
-
142
-
-
84861992072
-
A phase I study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma
-
(Suppl; Abstr 3021)
-
Moreno Garcia V, Baird RD, Shah KJ, Basu B, Tunariu N, Blanco M, Cassier PA, Pedersen JV, Puglisi M, Sarker D, Papadatos-Pastos D, Omlin AG, Biondo A, Ware JA, Koeppen H, Levy GG, Mazina KE, De Bono JS. A phase I study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma. J Clin Oncol. 2011;29. (Suppl; Abstr 3021).
-
(2011)
J Clin Oncol
, pp. 29
-
-
Moreno, G.V.1
Baird, R.D.2
Shah, K.J.3
Basu, B.4
Tunariu, N.5
Blanco, M.6
Cassier, P.A.7
Pedersen, J.V.8
Puglisi, M.9
Sarker, D.10
Papadatos-Pastos, D.11
Omlin, A.G.12
Biondo, A.13
Ware, J.A.14
Koeppen, H.15
Levy, G.G.16
Mazina, K.E.17
de Bono, J.S.18
-
143
-
-
77956566979
-
A phase I dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies
-
(Suppl; Abstr 3089)
-
Edelman G, Bedell C, Shapiro G, Pandya SS, Kwak EL, Scheffold C, Nguyen LT, Laird A, Baselga J, Rodon J. A phase I dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies. J Clin Oncol. 2010;28:15s(Suppl; Abstr 3089).
-
(2010)
J Clin Oncol
, vol.15 s
, pp. 28
-
-
Edelman, G.1
Bedell, C.2
Shapiro, G.3
Pandya, S.S.4
Kwak, E.L.5
Scheffold, C.6
Nguyen, L.T.7
Laird, A.8
Baselga, J.9
Rodon, J.10
-
144
-
-
33644685228
-
The phosphatidylinositol-3-kinase inhibitor PX-866 overcomes resistance to the epidermal growth factor receptor inhibitor gefitinib in A-549 human non-small cell lung cancer xenografts
-
Sep
-
Ihle NT, Paine-Murrieta G, Berggren MI, Baker A, Tate WR, Wipf P, Abraham RT, Kirkpatrick DL, Powis G. The phosphatidylinositol-3-kinase inhibitor PX-866 overcomes resistance to the epidermal growth factor receptor inhibitor gefitinib in A-549 human non-small cell lung cancer xenografts. Mol Cancer Ther. 2005 Sep;4(9):1349-1357.
-
(2005)
Mol Cancer Ther
, vol.4
, Issue.9
, pp. 1349-1357
-
-
Ihle, N.T.1
Paine-Murrieta, G.2
Berggren, M.I.3
Baker, A.4
Tate, W.R.5
Wipf, P.6
Abraham, R.T.7
Kirkpatrick, D.L.8
Powis, G.9
-
145
-
-
79952686437
-
Final results from a phase I, dose-escalation study of PX-866, an irreversible, pan-isoform inhibitor of PI3 kinase
-
(Suppl; Abstr 3089)
-
Jimeno A, Herbst RS, Falchook GS, Messersmith WA, Hecker S, Peterson S, Hausman DF, Kurzrock R, Eckhardt SG, Hong DS. Final results from a phase I, dose-escalation study of PX-866, an irreversible, pan-isoform inhibitor of PI3 kinase. J Clin Oncol. 2010;28:15s(Suppl; Abstr 3089).
-
(2010)
J Clin Oncol
, vol.28
-
-
Jimeno, A.1
Herbst, R.S.2
Falchook, G.S.3
Messersmith, W.A.4
Hecker, S.5
Peterson, S.6
Hausman, D.F.7
Kurzrock, R.8
Eckhardt, S.G.9
Hong, D.S.10
-
146
-
-
0030611198
-
P110delta, a novel phosphoinositide 3-kinase in leukocytes
-
Apr 29
-
Vanhaesebroeck B, Welham MJ, Kotani K, Stein R, Warne PH, Zvelebil MJ, Higashi K, Volinia S, Downward J, Waterfield MD. P110delta, a novel phosphoinositide 3-kinase in leukocytes. Proc Natl Acad Sci U S A. 1997 Apr 29;94(9):4330-4335.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, Issue.9
, pp. 4330-4335
-
-
Vanhaesebroeck, B.1
Welham, M.J.2
Kotani, K.3
Stein, R.4
Warne, P.H.5
Zvelebil, M.J.6
Higashi, K.7
Volinia, S.8
Downward, J.9
Waterfield, M.D.10
-
147
-
-
79958784935
-
Clinical Safety and Activity In a Phase 1 Study of CAL-101, An Isoform-Selective Inhibitor of Phosphatidylinositol 3-Kinase P110{delta}, In Patients with Relapsed or Refractory Non-Hodgkin Lymphoma
-
Kahl BS, Byrd JC, Flinn IW, Wagner-Johnston ND, Spurgeon SE, Benson DM, Furman RR, Brown JR, Coutre SE, Lannutti B, Giese NA, Ulrich RG, Webb HK, Peterman S, Holes LM, Yu AS. Clinical Safety and Activity In a Phase 1 Study of CAL-101, An Isoform-Selective Inhibitor of Phosphatidylinositol 3-Kinase P110{delta}, In Patients with Relapsed or Refractory Non-Hodgkin Lymphoma. Blood (ASH Annual Meeting Abstracts). 2010;116:1777.
-
(2010)
Blood (ASH Annual Meeting Abstracts)
, vol.116
, pp. 1777
-
-
Kahl, B.S.1
Byrd, J.C.2
Flinn, I.W.3
Wagner-Johnston, N.D.4
Spurgeon, S.E.5
Benson, D.M.6
Furman, R.R.7
Brown, J.R.8
Coutre, S.E.9
Lannutti, B.10
Giese, N.A.11
Ulrich, R.G.12
Webb, H.K.13
Peterman, S.14
Holes, L.M.15
Yu, A.S.16
-
148
-
-
79953655788
-
CAL- 101, An Isoform-Selective Inhibitor of Phosphatidylinositol 3-Kinase P110{delta}, Demonstrates Clinical Activity and Pharmacodynamic Effects In Patients with Relapsed or Refractory Chronic Lymphocytic Leukemia
-
Furman RR, Byrd JC, Brown JR, Coutre SE, Benson DM, Wagner-Johnston ND, Flinn IW, Kahl BS, Spurgeon SE, Lannutti B, Giese NA, Webb HK, Ulrich RG, Peterman S, Holes LM, Yu AS. CAL- 101, An Isoform-Selective Inhibitor of Phosphatidylinositol 3-Kinase P110{delta}, Demonstrates Clinical Activity and Pharmacodynamic Effects In Patients with Relapsed or Refractory Chronic Lymphocytic Leukemia. Blood (ASH Annual Meeting Abstracts). 2010;116:55.
-
(2010)
Blood (ASH Annual Meeting Abstracts)
, vol.116
, pp. 55
-
-
Furman, R.R.1
Byrd, J.C.2
Brown, J.R.3
Coutre, S.E.4
Benson, D.M.5
Wagner-Johnston, N.D.6
Flinn, I.W.7
Kahl, B.S.8
Spurgeon, S.E.9
Lannutti, B.10
Giese, N.A.11
Webb, H.K.12
Ulrich, R.G.13
Peterman, S.14
Holes, L.M.15
Yu, A.S.16
-
149
-
-
34548596728
-
A dual phosphoinositide-3-kinase alpha/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma
-
Sep 1
-
Fan QW, Cheng CK, Nicolaides TP, Hackett CS, Knight ZA, Shokat KM, Weiss WA. A dual phosphoinositide-3-kinase alpha/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma. Cancer Res. 2007 Sep 1;67(17):7960-7965.
-
(2007)
Cancer Res
, vol.67
, Issue.17
, 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
-
150
-
-
34250823572
-
Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases
-
Jun 15
-
Raynaud FI, Eccles S, Clarke PA, Hayes A, Nutley B, Alix S, Henley A, Di-Stefano F, Ahmad Z, Guillard S, Bjerke LM, Kelland L, Valenti M, Patterson L, Gowan S, de Haven Brandon A, Hayakawa M, Kaizawa H, Koizumi T, Ohishi T, Patel S, Saghir N, Parker P, Waterfield M, Workman P. Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases. Cancer Res. 2007 Jun 15;67(12):5840-5850.
-
(2007)
Cancer Res
, vol.67
, Issue.12
, pp. 5840-5850
-
-
Raynaud, F.I.1
Eccles, S.2
Clarke, P.A.3
Hayes, A.4
Nutley, B.5
Alix, S.6
Henley, A.7
Di-Stefano, F.8
Ahmad, Z.9
Guillard, S.10
Bjerke, L.M.11
Kelland, L.12
Valenti, M.13
Patterson, L.14
Gowan, S.15
de Haven Brandon, A.16
Hayakawa, M.17
Kaizawa, H.18
Koizumi, T.19
Ohishi, T.20
Patel, S.21
Saghir, N.22
Parker, P.23
Waterfield, M.24
Workman, P.25
more..
-
151
-
-
79960605738
-
Targeting phosphatidylinositol 3 kinase (PI3K)-Akt beyond rapalogs
-
May 6
-
Ogita S, Lorusso P. Targeting phosphatidylinositol 3 kinase (PI3K)-Akt beyond rapalogs. Targeted oncology. 2011 May 6.
-
(2011)
Targeted Oncology
-
-
Ogita, S.1
Lorusso, P.2
-
152
-
-
43749120045
-
DNA repair deficiency as a therapeutic target in cancer
-
Feb
-
Martin SA, Lord CJ, Ashworth A. DNA repair deficiency as a therapeutic target in cancer. Curr Opin Genet Dev. 2008 Feb;18(1):80-86.
-
(2008)
Curr Opin Genet Dev
, vol.18
, Issue.1
, pp. 80-86
-
-
Martin, S.A.1
Lord, C.J.2
Ashworth, A.3
-
153
-
-
0031105972
-
D-21266, a new heterocyclic alkylphospholipid with antitumour activity
-
Mar
-
Hilgard P, Klenner T, Stekar J, Nossner G, Kutscher B, Engel J. D-21266, a new heterocyclic alkylphospholipid with antitumour activity. Eur J Cancer. 1997 Mar;33(3):442-446.
-
(1997)
Eur J Cancer
, vol.33
, Issue.3
, pp. 442-446
-
-
Hilgard, P.1
Klenner, T.2
Stekar, J.3
Nossner, G.4
Kutscher, B.5
Engel, J.6
-
154
-
-
52449092107
-
Breast tumor cells with PI3K mutation or HER2 amplification are selectively addicted to Akt signaling
-
She QB, Chandarlapaty S, Ye Q, Lobo J, Haskell KM, Leander KR, DeFeo-Jones D, Huber HE, Rosen N. Breast tumor cells with PI3K mutation or HER2 amplification are selectively addicted to Akt signaling. PLoS ONE. 2008;3(8):e3065.
-
(2008)
PLoS ONE
, vol.3
, Issue.8
-
-
She, Q.B.1
Chandarlapaty, S.2
Ye, Q.3
Lobo, J.4
Haskell, K.M.5
Leander, K.R.6
Defeo-Jones, D.7
Huber, H.E.8
Rosen, N.9
-
155
-
-
77953721226
-
An allosteric Akt inhibitor effectively blocks Akt signaling and tumor growth with only transient effects on glucose and insulin levels in vivo
-
Apr
-
Cherrin C, Haskell K, Howell B, Jones R, Leander K, Robinson R, Watkins A, Bilodeau M, Hoffman J, Sanderson P, Hartman G, Mahan E, Prueksaritanont T, Jiang G, She QB, Rosen N, Sepp-Lorenzino L, Defeo-Jones D, Huber HE. An allosteric Akt inhibitor effectively blocks Akt signaling and tumor growth with only transient effects on glucose and insulin levels in vivo. Cancer Biol Ther. 2010 Apr;9(7):493-503.
-
(2010)
Cancer Biol Ther
, vol.9
, Issue.7
, pp. 493-503
-
-
Cherrin, C.1
Haskell, K.2
Howell, B.3
Jones, R.4
Leander, K.5
Robinson, R.6
Watkins, A.7
Bilodeau, M.8
Hoffman, J.9
Sanderson, P.10
Hartman, G.11
Mahan, E.12
Prueksaritanont, T.13
Jiang, G.14
She, Q.B.15
Rosen, N.16
Sepp-Lorenzino, L.17
Defeo-Jones, D.18
Huber, H.E.19
-
156
-
-
70350435062
-
Antitumor activity of a novel antisense oligonucleotide against Akt1
-
Nov
-
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 Nov 1;108(4):832-838.
-
(2009)
J Cell Biochem
, vol.108
, Issue.4
, 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
-
157
-
-
77957833800
-
The Akt activation inhibitor TCN-P inhibits Akt phosphorylation by binding to the PH domain of Akt and blocking its recruitment to the plasma membrane
-
Nov
-
Berndt N, Yang H, Trinczek B, Betzi S, Zhang Z, Wu B, Lawrence NJ, Pellecchia M, Schonbrunn E, Cheng JQ, Sebti SM. The Akt activation inhibitor TCN-P inhibits Akt phosphorylation by binding to the PH domain of Akt and blocking its recruitment to the plasma membrane. Cell Death Differ. 2010 Nov;17(11):1795-1804.
-
(2010)
Cell Death Differ
, vol.17
, Issue.11
, pp. 1795-1804
-
-
Berndt, N.1
Yang, H.2
Trinczek, B.3
Betzi, S.4
Zhang, Z.5
Wu, B.6
Lawrence, N.J.7
Pellecchia, M.8
Schonbrunn, E.9
Cheng, J.Q.10
Sebti, S.M.11
-
158
-
-
0027333359
-
A phase II trial of trial of tricyclic nucleoside phosphate in patients with advanced squamous cell carcinoma of the cervix. A Gynecologic Oncology Group Study
-
Dec
-
Feun LG, Blessing JA, Barrett RJ, Hanjani P. A phase II trial of tricyclic nucleoside phosphate in patients with advanced squamous cell carcinoma of the cervix. A Gynecologic Oncology Group Study. Am J Clin Oncol. 1993 Dec;16(6):506-508.
-
(1993)
Am J Clin Oncol
, vol.16
, Issue.6
, pp. 506-508
-
-
Feun, L.G.1
Blessing, J.A.2
Barrett, R.J.3
Hanjani, P.A.4
-
159
-
-
0029656181
-
Phase I-II study: Triciribine (tricyclic nucleoside phosphate) for metastatic breast cancer
-
Hoffman K, Holmes FA, Fraschini G, Esparza L, Frye D, Raber MN, Newman RA, Hortobagyi GN. Phase I-II study: triciribine (tricyclic nucleoside phosphate) for metastatic breast cancer. Cancer Chemother Pharmacol. 1996;37(3):254-258.
-
(1996)
Cancer Chemother Pharmacol
, vol.37
, Issue.3
, pp. 254-258
-
-
Hoffman, K.1
Holmes, F.A.2
Fraschini, G.3
Esparza, L.4
Frye, D.5
Raber, M.N.6
Newman, R.A.7
Hortobagyi, G.N.8
-
160
-
-
84861635942
-
Phase I pharmacokinetic and pharmacodynamic study of triciribine phosphate monohydrate, a small-molecule inhibitor of AKT phosphorylation, in adult subjects with solid tumors containing activated AKT
-
Jul 20
-
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 monohydrate, a small-molecule inhibitor of AKT phosphorylation, in adult subjects with solid tumors containing activated AKT. Invest New Drugs. 2010 Jul 20.
-
(2010)
Invest New Drugs
-
-
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
-
161
-
-
33751002361
-
Phase II study of daily oral perifosine in patients with advanced soft tissue sarcoma
-
Nov 15
-
Bailey HH, Mahoney MR, Ettinger DS, Maples WJ, Fracasso PM, Traynor AM, Erlichman C, Okuno SH. Phase II study of daily oral perifosine in patients with advanced soft tissue sarcoma. Cancer. 2006 Nov 15;107(10):2462-2467.
-
(2006)
Cancer
, vol.107
, Issue.10
, pp. 2462-2467
-
-
Bailey, H.H.1
Mahoney, M.R.2
Ettinger, D.S.3
Maples, W.J.4
Fracasso, P.M.5
Traynor, A.M.6
Erlichman, C.7
Okuno, S.H.8
-
162
-
-
76049121742
-
Clinical and translational studies of a phase II trial of the novel oral Akt inhibitor perifosine in relapsed or relapsed/refractory Waldenstrom's macroglobulinemia
-
Feb 1
-
Ghobrial IM, Roccaro A, Hong F, Weller E, Rubin N, Leduc R, Rourke M, Chuma S, Sacco A, Jia X, Azab F, Azab AK, Rodig S, Warren D, Harris B, Varticovski L, Sportelli P, Leleu X, Anderson KC, Richardson PG. Clinical and translational studies of a phase II trial of the novel oral Akt inhibitor perifosine in relapsed or relapsed/refractory Waldenstrom's macroglobulinemia. Clin Cancer Res. 2010 Feb 1;16(3):1033-1041.
-
(2010)
Clin Cancer Res
, vol.16
, Issue.3
, pp. 1033-1041
-
-
Ghobrial, I.M.1
Roccaro, A.2
Hong, F.3
Weller, E.4
Rubin, N.5
Leduc, R.6
Rourke, M.7
Chuma, S.8
Sacco, A.9
Jia, X.10
Azab, F.11
Azab, A.K.12
Rodig, S.13
Warren, D.14
Harris, B.15
Varticovski, L.16
Sportelli, P.17
Leleu, X.18
Anderson, K.C.19
Richardson, P.G.20
more..
-
163
-
-
38949099997
-
The AKT inhibitor perifosine in biochemically recurrent prostate cancer: A phase II California/Pittsburgh cancer consortium trial
-
Dec
-
Chee KG, Longmate J, Quinn DI, Chatta G, Pinski J, Twardowski P, Pan CX, Cambio A, Evans CP, Gandara DR, Lara PN, Jr. The AKT inhibitor perifosine in biochemically recurrent prostate cancer: a phase II California/Pittsburgh cancer consortium trial. Clin Genitourin Cancer. 2007 Dec;5(7):433-437.
-
(2007)
Clin Genitourin Cancer
, vol.5
, Issue.7
, pp. 433-437
-
-
Chee, K.G.1
Longmate, J.2
Quinn, D.I.3
Chatta, G.4
Pinski, J.5
Twardowski, P.6
Pan, C.X.7
Cambio, A.8
Evans, C.P.9
Gandara, D.R.10
Lara Jr., P.N.11
-
164
-
-
43049107243
-
A Phase 2 study of perifosine in advanced or metastatic breast cancer
-
Mar
-
Leighl NB, Dent S, Clemons M, Vandenberg TA, Tozer R, Warr DG, Crump RM, Hedley D, Pond GR, Dancey JE, Moore MJ. A Phase 2 study of perifosine in advanced or metastatic breast cancer. Breast Cancer Res Treat. 2008 Mar;108(1):87-92.
-
(2008)
Breast Cancer Res Treat
, vol.108
, Issue.1
, pp. 87-92
-
-
Leighl, N.B.1
Dent, S.2
Clemons, M.3
Vandenberg, T.A.4
Tozer, R.5
Warr, D.G.6
Crump, R.M.7
Hedley, D.8
Pond, G.R.9
Dancey, J.E.10
Moore, M.J.11
-
165
-
-
33751184394
-
A phase II trial of perifosine, an oral alkylphospholipid, in recurrent or metastatic head and neck cancer
-
Jul
-
Argiris A, Cohen E, Karrison T, Esparaz B, Mauer A, Ansari R, Wong S, Lu Y, Pins M, Dancey J, Vokes E. A phase II trial of perifosine, an oral alkylphospholipid, in recurrent or metastatic head and neck cancer. Cancer Biol Ther. 2006 Jul;5(7):766-770.
-
(2006)
Cancer Biol Ther
, vol.5
, Issue.7
, pp. 766-770
-
-
Argiris, A.1
Cohen, E.2
Karrison, T.3
Esparaz, B.4
Mauer, A.5
Ansari, R.6
Wong, S.7
Lu, Y.8
Pins, M.9
Dancey, J.10
Vokes, E.11
-
166
-
-
27744450731
-
A phase II study of perifosine in androgen independent prostate cancer
-
Oct
-
Posadas EM, Gulley J, Arlen PM, Trout A, Parnes HL, Wright J, Lee MJ, Chung EJ, Trepel JB, Sparreboom A, Chen C, Jones E, Steinberg SM, Daniels A, Figg WD, Dahut WL. A phase II study of perifosine in androgen independent prostate cancer. Cancer Biol Ther. 2005 Oct;4(10):1133-1137.
-
(2005)
Cancer Biol Ther
, vol.4
, Issue.10
, pp. 1133-1137
-
-
Posadas, E.M.1
Gulley, J.2
Arlen, P.M.3
Trout, A.4
Parnes, H.L.5
Wright, J.6
Lee, M.J.7
Chung, E.J.8
Trepel, J.B.9
Sparreboom, A.10
Chen, C.11
Jones, E.12
Steinberg, S.M.13
Daniels, A.14
Figg, W.D.15
Dahut, W.L.A.16
-
167
-
-
31544448600
-
Phase II study of perifosine in previously untreated patients with metastatic melanoma
-
Dec
-
Ernst DS, Eisenhauer E, Wainman N, Davis M, Lohmann R, Baetz T, Belanger K, Smylie M. Phase II study of perifosine in previously untreated patients with metastatic melanoma. Invest New Drugs. 2005 Dec;23(6):569-575.
-
(2005)
Invest New Drugs
, vol.23
, Issue.6
, pp. 569-575
-
-
Ernst, D.S.1
Eisenhauer, E.2
Wainman, N.3
Davis, M.4
Lohmann, R.5
Baetz, T.6
Belanger, K.7
Smylie, M.8
-
168
-
-
79953852883
-
The Akt-specific inhibitor MK2206 selectively inhibits thyroid cancer cells harboring mutations that can activate the PI3K/Akt pathway
-
Apr
-
Liu R, Liu D, Trink E, Bojdani E, Ning G, Xing M. The Akt-specific inhibitor MK2206 selectively inhibits thyroid cancer cells harboring mutations that can activate the PI3K/Akt pathway. J Clin Endocrinol Metab. 2011 Apr;96(4):E577-E585.
-
(2011)
J Clin Endocrinol Metab
, vol.96
, Issue.4
-
-
Liu, R.1
Liu, D.2
Trink, E.3
Bojdani, E.4
Ning, G.5
Xing, M.6
-
169
-
-
79955504184
-
Combination of farnesyltransferase and Akt inhibitors is synergistic in breast cancer cells and causes significant breast tumor regression in ErbB2 transgenic mice
-
May 1
-
Balasis ME, Forinash KD, Chen YA, Fulp WJ, Coppola D, Hamilton AD, Cheng JQ, Sebti SM. Combination of farnesyltransferase and Akt inhibitors is synergistic in breast cancer cells and causes significant breast tumor regression in ErbB2 transgenic mice. Clin Cancer Res. 2011 May 1;17(9):2852-2862.
-
(2011)
Clin Cancer Res
, vol.17
, Issue.9
, pp. 2852-2862
-
-
Balasis, M.E.1
Forinash, K.D.2
Chen, Y.A.3
Fulp, W.J.4
Coppola, D.5
Hamilton, A.D.6
Cheng, J.Q.7
Sebti, S.M.8
-
170
-
-
78649729548
-
Combination treatment with MEK and AKT inhibitors is more effective than each drug alone in human non-small cell lung cancer in vitro and in vivo
-
Meng J, Dai B, Fang B, Bekele BN, Bornmann WG, Sun D, Peng Z, Herbst RS, Papadimitrakopoulou V, Minna JD, Peyton M, Roth JA. Combination treatment with MEK and AKT inhibitors is more effective than each drug alone in human non-small cell lung cancer in vitro and in vivo. PLoS ONE. 2010;5(11):e14124.
-
(2010)
PLoS ONE
, vol.5
, Issue.11
-
-
Meng, J.1
Dai, B.2
Fang, B.3
Bekele, B.N.4
Bornmann, W.G.5
Sun, D.6
Peng, Z.7
Herbst, R.S.8
Papadimitrakopoulou, V.9
Minna, J.D.10
Peyton, M.11
Roth, J.A.12
-
171
-
-
77954615408
-
MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
-
Jul
-
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 Jul;9(7):1956-1967.
-
(2010)
Mol Cancer Ther
, vol.9
, Issue.7
, 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
-
172
-
-
68049132168
-
A phase I study of MK-2206, an oral potent allosteric Akt inhibitor (Akti), in patients (pts) with advanced solid tumor (ST)
-
Suppl; Abstr 3503
-
Tolcher AW, Yap TA, Fearen I, Taylor A, Carpenter C, Brunetto AT, Beeram M, Papadopoulos K, Yan L, de Bono J. A phase I study of MK-2206, an oral potent allosteric Akt inhibitor (Akti), in patients (pts) with advanced solid tumor (ST). J Clin Oncol. 2009;27:15s(Suppl; Abstr 3503).
-
(2009)
J Clin Oncol
, vol.15 s
, pp. 27
-
-
Tolcher, A.W.1
Yap, T.A.2
Fearen, I.3
Taylor, A.4
Carpenter, C.5
Brunetto, A.T.6
Beeram, M.7
Papadopoulos, K.8
Yan, L.9
de Bono, J.10
-
173
-
-
77956587792
-
First-in-class phase I trial of a selective Akt inhibitor, MK2206 (MK), evaluating alternate day (QOD) and once weekly (QW) doses in advanced cancer patients (pts) with evidence of target modulation and antitumor activity
-
Suppl; Abstr 3009
-
Yap TA, Patnaik A, Fearen I, Olmos D, Papadopoulos K, Tunariu N, Sullivan D, Yan L, De Bono JS, Tolcher AW. First-in-class phase I trial of a selective Akt inhibitor, MK2206 (MK), evaluating alternate day (QOD) and once weekly (QW) doses in advanced cancer patients (pts) with evidence of target modulation and antitumor activity. J Clin Oncol. 2010;28:15s(Suppl; Abstr 3009).
-
(2010)
J Clin Oncol
, vol.15 s
, pp. 28
-
-
Yap, T.A.1
Patnaik, A.2
Fearen, I.3
Olmos, D.4
Papadopoulos, K.5
Tunariu, N.6
Sullivan, D.7
Yan, L.8
de Bono, J.S.9
Tolcher, A.W.10
-
174
-
-
84874659112
-
A phase I study of the AKT inhibitor (MK-2206) with concurrent trastuzumab and lapatinib in patients with HER2-positive solid tumors
-
Suppl; Abstr 3028
-
Han HS, Swanton C, Janjigian YY, Sutherland SC, Chandarlapaty S, Lehman R, Hamilton N, Knowles J, Lee R, Yan L, Sullivan D, Hudis C, Lee H. A phase I study of the AKT inhibitor (MK-2206) with concurrent trastuzumab and lapatinib in patients with HER2-positive solid tumors J Clin Oncol. 2011;29(Suppl; Abstr 3028).
-
(2011)
J Clin Oncol
, vol.29
-
-
Han, H.S.1
Swanton, C.2
Janjigian, Y.Y.3
Sutherland, S.C.4
Chandarlapaty, S.5
Lehman, R.6
Hamilton, N.7
Knowles, J.8
Lee, R.9
Yan, L.10
Sullivan, D.11
Hudis, C.12
Lee, H.13
-
175
-
-
80054747639
-
Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase I first-in-human study
-
Suppl; Abstr 3003
-
Burris HA, Siu LL, Infante JR, Wheler JJ, Kurkjian C, Opalinska J, Smith DA, Antal JM, Gauvin JL, Gonzalez T, Adams LM, Bedard P, Gerecitano JF, Kurzrock R, Moore KN, Morris SR, Aghajanian C. Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase I first-in-human study. J Clin Oncol. 2011;29(Suppl; Abstr 3003).
-
(2011)
J Clin Oncol
, vol.29
-
-
Burris, H.A.1
Siu, L.L.2
Infante, J.R.3
Wheler, J.J.4
Kurkjian, C.5
Opalinska, J.6
Smith, D.A.7
Antal, J.M.8
Gauvin, J.L.9
Gonzalez, T.10
Adams, L.M.11
Bedard, P.12
Gerecitano, J.F.13
Kurzrock, R.14
Moore, K.N.15
Morris, S.R.16
Aghajanian, C.17
-
176
-
-
84856303672
-
Phase I dose-escalation of the oral MEK1/2 inhibitor GSK1120212 (GSK212) dosed in combination with the oral AKT inhibitor GSK2141795 (GSK795)
-
Suppl; Abstr 3085
-
Kurzrock R, Patnaik A, Rosenstein L, Fu S, Papadopoulos KP, Smith DA, Falchook GS, Chambers G, Gauvin JL, Naing A, Smith LS, Gonzalez T, Tsimberidou AM, Mays TA, Cox DS, Hong DS, DeMarini DJ, Le NT, Morris SR, Tolcher AW. Phase I dose-escalation of the oral MEK1/2 inhibitor GSK1120212 (GSK212) dosed in combination with the oral AKT inhibitor GSK2141795 (GSK795). J Clin Oncol. 2011;29(Suppl; Abstr 3085).
-
(2011)
J Clin Oncol
, vol.29
-
-
Kurzrock, R.1
Patnaik, A.2
Rosenstein, L.3
Fu, S.4
Papadopoulos, K.P.5
Smith, D.A.6
Falchook, G.S.7
Chambers, G.8
Gauvin, J.L.9
Naing, A.10
Smith, L.S.11
Gonzalez, T.12
Tsimberidou, A.M.13
Mays, T.A.14
Cox, D.S.15
Hong, D.S.16
Demarini, D.J.17
Le, N.T.18
Morris, S.R.19
Tolcher, A.W.20
more..
-
177
-
-
57749188299
-
Targeting cancer with small molecule kinase inhibitors
-
Jan
-
Zhang J, Yang PL, Gray NS. Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer. 2009 Jan;9(1):28-39.
-
(2009)
Nat Rev Cancer
, vol.9
, Issue.1
, pp. 28-39
-
-
Zhang, J.1
Yang, P.L.2
Gray, N.S.3
-
178
-
-
33750510023
-
A phase II clinical and pharmacodynamic study of temsirolimus in advanced neuroendocrine carcinomas
-
Nov 6
-
Duran I, Kortmansky J, Singh D, Hirte H, Kocha W, Goss G, Le L, Oza A, Nicklee T, Ho J, Birle D, Pond GR, Arboine D, Dancey J, Aviel-Ronen S, Tsao MS, Hedley D, Siu LL. A phase II clinical and pharmacodynamic study of temsirolimus in advanced neuroendocrine carcinomas. Br J Cancer. 2006 Nov 6;95(9):1148-1154.
-
(2006)
Br J Cancer
, vol.95
, Issue.9
, pp. 1148-1154
-
-
Duran, I.1
Kortmansky, J.2
Singh, D.3
Hirte, H.4
Kocha, W.5
Goss, G.6
Le, L.7
Oza, A.8
Nicklee, T.9
Ho, J.10
Birle, D.11
Pond, G.R.12
Arboine, D.13
Dancey, J.14
Aviel-Ronen, S.15
Tsao, M.S.16
Hedley, D.17
Siu, L.L.18
-
179
-
-
43249131245
-
Dose- and scheduledependent inhibition of the mammalian target of rapamycin pathway with everolimus: A phase I tumor pharmacodynamic study in patients with advanced solid tumors
-
Apr 1
-
Tabernero J, Rojo F, Calvo E, Burris H, Judson I, Hazell K, Martinelli E, Ramon y Cajal S, Jones S, Vidal L, Shand N, Macarulla T, Ramos FJ, Dimitrijevic S, Zoellner U, Tang P, Stumm M, Lane HA, Lebwohl D, Baselga J. Dose- and scheduledependent inhibition of the mammalian target of rapamycin pathway with everolimus: a phase I tumor pharmacodynamic study in patients with advanced solid tumors. J Clin Oncol. 2008 Apr 1;26(10):1603-1610.
-
(2008)
J Clin Oncol
, vol.26
, Issue.10
, pp. 1603-1610
-
-
Tabernero, J.1
Rojo, F.2
Calvo, E.3
Burris, H.4
Judson, I.5
Hazell, K.6
Martinelli, E.7
Ramon8
Cajal, S.9
Jones, S.10
Vidal, L.11
Shand, N.12
Macarulla, T.13
Ramos, F.J.14
Dimitrijevic, S.15
Zoellner, U.16
Tang, P.17
Stumm, M.18
Lane, H.A.19
Lebwohl, D.20
Baselga, J.21
more..
-
180
-
-
54749095517
-
Enhancing mammalian target of rapamycin (mTOR)-targeted cancer therapy by preventing mTOR/raptor inhibition-initiated, mTOR/rictorindependent Akt activation
-
Sep 15
-
Wang X, Yue P, Kim YA, Fu H, Khuri FR, Sun SY. Enhancing mammalian target of rapamycin (mTOR)-targeted cancer therapy by preventing mTOR/raptor inhibition-initiated, mTOR/rictorindependent Akt activation. Cancer Res. 2008 Sep 15;68(18):7409-7418.
-
(2008)
Cancer Res
, vol.68
, Issue.18
, pp. 7409-7418
-
-
Wang, X.1
Yue, P.2
Kim, Y.A.3
Fu, H.4
Khuri, F.R.5
Sun, S.Y.6
-
181
-
-
58149136153
-
Overcoming mTOR inhibition-induced paradoxical activation of survival signaling pathways enhances mTOR inhibitors' anticancer efficacy
-
Dec
-
Wang X, Hawk N, Yue P, Kauh J, Ramalingam SS, Fu H, Khuri FR, Sun SY. Overcoming mTOR inhibition-induced paradoxical activation of survival signaling pathways enhances mTOR inhibitors' anticancer efficacy. Cancer Biol Ther. 2008 Dec;7(12):1952-1958.
-
(2008)
Cancer Biol Ther
, vol.7
, Issue.12
, pp. 1952-1958
-
-
Wang, X.1
Hawk, N.2
Yue, P.3
Kauh, J.4
Ramalingam, S.S.5
Fu, H.6
Khuri, F.R.7
Sun, S.Y.8
-
182
-
-
79959795786
-
Improved survival with vemurafenib in melanoma with BRAF V600E mutation
-
Jun 30
-
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, O'Day SJ, Sosman JA, Kirkwood JM, Eggermont AM, Dreno B, Nolop K, Li J, Nelson B, Hou J, Lee RJ, Flaherty KT, McArthur GA. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011 Jun 30;364(26):2507-2516.
-
(2011)
N Engl J Med
, vol.364
, Issue.26
, 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
O'Day, S.J.17
Sosman, J.A.18
Kirkwood, J.M.19
Eggermont, A.M.20
Dreno, B.21
Nolop, K.22
Li, J.23
Nelson, B.24
Hou, J.25
Lee, R.J.26
Flaherty, K.T.27
McArthur, G.A.28
more..
-
183
-
-
2342624080
-
EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
-
Jun 4
-
Paez JG, Janne PA, Lee JC, Tracy S, Greulich H, Gabriel S, Herman P, Kaye FJ, Lindeman N, Boggon TJ, Naoki K, Sasaki H, Fujii Y, Eck MJ, Sellers WR, Johnson BE, Meyerson M. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science. 2004 Jun 4;304(5676):1497-1500.
-
(2004)
Science
, vol.304
, Issue.5676
, pp. 1497-1500
-
-
Paez, J.G.1
Janne, P.A.2
Lee, J.C.3
Tracy, S.4
Greulich, H.5
Gabriel, S.6
Herman, P.7
Kaye, F.J.8
Lindeman, N.9
Boggon, T.J.10
Naoki, K.11
Sasaki, H.12
Fujii, Y.13
Eck, M.J.14
Sellers, W.R.15
Johnson, B.E.16
Meyerson, M.17
-
184
-
-
77949484879
-
Inhibition profiles of phosphatidylinositol 3-kinase inhibitors against PI3K superfamily and human cancer cell line panel JFCR39
-
Apr
-
Kong D, Dan S, Yamazaki K, Yamori T. Inhibition profiles of phosphatidylinositol 3-kinase inhibitors against PI3K superfamily and human cancer cell line panel JFCR39. Eur J Cancer. 2010 Apr;46(6):1111-1121.
-
(2010)
Eur J Cancer
, vol.46
, Issue.6
, pp. 1111-1121
-
-
Kong, D.1
Dan, S.2
Yamazaki, K.3
Yamori, T.4
-
185
-
-
79960587911
-
Clinical activity of mammalian target of rapamycin inhibitors in solid tumors
-
Jun
-
Alvarado Y, Mita MM, Vemulapalli S, Mahalingam D, Mita AC. Clinical activity of mammalian target of rapamycin inhibitors in solid tumors. Target Oncol. 2011 Jun;6(2):69-94.
-
(2011)
Target Oncol
, vol.6
, Issue.2
, pp. 69-94
-
-
Alvarado, Y.1
Mita, M.M.2
Vemulapalli, S.3
Mahalingam, D.4
Mita, A.C.5
|