-
1
-
-
34548097240
-
AZD6244 (ARRY-142886), a potent inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 kinases: Mechanism of action in vivo, pharmacokinetic/pharmacodynamic relationship, and potential for combination in preclinical models
-
DOI 10.1158/1535-7163.MCT-07-0231
-
Davies BR, Logie A, McKay JS, Martin P, Steele S, Jenkins R, et al. AZD6244 (ARRY-142886), a potent inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 kinases: mechanism of action in vivo, pharmacokinetic/pharmacodynamic relationship, and potential for combination in preclinical models. Mol Cancer Ther 2007;6:2209-19. (Pubitemid 47294749)
-
(2007)
Molecular Cancer Therapeutics
, vol.6
, Issue.8
, pp. 2209-2219
-
-
Davies, B.R.1
Logie, A.2
McKay, J.S.3
Martin, P.4
Steele, S.5
Jenkins, R.6
Cockerill, M.7
Cartlidge, S.8
Smith, P.D.9
-
2
-
-
34247278727
-
Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy
-
DOI 10.1038/sj.bjc.6603685, PII 6603685
-
Di Fiore F, Blanchard F, Charbonnier F, Le Pessot F, Lamy A, Galais MP, et al. Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy. Br J Cancer 2007;96:1166-9. (Pubitemid 46625066)
-
(2007)
British Journal of Cancer
, vol.96
, Issue.8
, pp. 1166-1169
-
-
Di, F.F.1
Blanchard, F.2
Charbonnier, F.3
Le, P.F.4
Lamy, A.5
Galais, M.P.6
Bastit, L.7
Killian, A.8
Sesboue, R.9
Tuech, J.J.10
Queuniet, A.M.11
Paillot, B.12
Sabourin, J.C.13
Michot, F.14
Michel, P.15
Frebourg, T.16
-
3
-
-
66749120729
-
A gene expression predictor of response to EGFR-targeted therapy stratifies progression-free survival to cetuximab in KRAS wild-type metastatic colorectal cancer
-
Balko JM, Black EP. A gene expression predictor of response to EGFR-targeted therapy stratifies progression-free survival to cetuximab in KRAS wild-type metastatic colorectal cancer. BMC Cancer 2009;9:145.
-
(2009)
BMC Cancer
, vol.9
, pp. 145
-
-
Balko, J.M.1
Black, E.P.2
-
4
-
-
64649092674
-
Health-related quality of life in patients with advanced colorectal cancer treated with cetuximab: Overall and KRAS-specific results of the NCIC CTG and AGITG CO.17 Trial
-
Au HJ, Karapetis CS, O'Callaghan CJ, Tu D, Moore MJ, Zalcberg JR, et al. Health-related quality of life in patients with advanced colorectal cancer treated with cetuximab: overall and KRAS-specific results of the NCIC CTG and AGITG CO.17 Trial. J Clin Oncol 2009;27:1822-8.
-
(2009)
J Clin Oncol
, vol.27
, pp. 1822-1828
-
-
Au, H.J.1
Karapetis, C.S.2
O'Callaghan, C.J.3
Tu, D.4
Moore, M.J.5
Zalcberg, J.R.6
-
5
-
-
57449095367
-
Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer
-
Di Nicolantonio F, Martini M, Molinari F, Sartore-Bianchi A, Arena S, Saletti P, et al. Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer. J Clin Oncol 2008;26:5705-12.
-
(2008)
J Clin Oncol
, vol.26
, pp. 5705-5712
-
-
Di Nicolantonio, F.1
Martini, M.2
Molinari, F.3
Sartore-Bianchi, A.4
Arena, S.5
Saletti, P.6
-
6
-
-
51049113834
-
BRAF V600E disrupts AZD6244-induced abrogation of negative feedback pathways between extracellular signal-regulated kinase and Raf proteins
-
Friday BB, Yu C, Dy GK, Smith PD, Wang L, Thibodeau SN, et al. BRAF V600E disrupts AZD6244-induced abrogation of negative feedback pathways between extracellular signal-regulated kinase and Raf proteins. Cancer Res 2008;68:6145-53.
-
(2008)
Cancer Res
, vol.68
, pp. 6145-6153
-
-
Friday, B.B.1
Yu, C.2
Dy, G.K.3
Smith, P.D.4
Wang, L.5
Thibodeau, S.N.6
-
7
-
-
43749103335
-
Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers
-
Adjei AA, Cohen RB, Franklin W, Morris C, Wilson D, Molina JR, et al. Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers. J Clin Oncol 2008;26:2139-46.
-
(2008)
J Clin Oncol
, vol.26
, pp. 2139-2146
-
-
Adjei, A.A.1
Cohen, R.B.2
Franklin, W.3
Morris, C.4
Wilson, D.5
Molina, J.R.6
-
8
-
-
84855487013
-
A phase II, open-label, randomized study to assess the efficacy and safety of AZD6244 (ARRY-142886) versus capecitabine monotherapy in patients with colorectal cancer who have failed one or two prior chemotherapeutic regimens
-
Bennouna J, Lang I, Valladares-Ayerbes M, Boer K, Adenis A, Escudero P, et al. A phase II, open-label, randomized study to assess the efficacy and safety of AZD6244 (ARRY-142886) versus capecitabine monotherapy in patients with colorectal cancer who have failed one or two prior chemotherapeutic regimens. Invest New Drug 2011;29:1021-8.
-
(2011)
Invest New Drug
, vol.29
, pp. 1021-1028
-
-
Bennouna, J.1
Lang, I.2
Valladares-Ayerbes, M.3
Boer, K.4
Adenis, A.5
Escudero, P.6
-
9
-
-
65649108998
-
AZD6244 (ARRY-142886) vs temozolomide (TMZ) in patients (pts) with advanced melanoma: An open-label, randomized, multicenter, phase II study
-
Abstract 9033
-
Dummer R, Robert C, Chapman PB, Sosman JA, Middleton M, Bastholt L, et al. AZD6244 (ARRY-142886) vs temozolomide (TMZ) in patients (pts) with advanced melanoma: an open-label, randomized, multicenter, phase II study. J Clin Oncol 2008;26(15 Suppl):Abstract 9033.
-
(2008)
J Clin Oncol
, vol.26
, Issue.15 SUPPL.
-
-
Dummer, R.1
Robert, C.2
Chapman, P.B.3
Sosman, J.A.4
Middleton, M.5
Bastholt, L.6
-
10
-
-
77958198647
-
A phase II, open-label, randomized study to assess the efficacy and safety of AZD6244 (ARRY-142886) versus pemetrexed in patients with non-small cell lung cancer who have failed one or two prior chemotherapeutic regimens
-
Hainsworth JD, Cebotaru CL, Kanarev V, Ciuleanu TE, Damyanov D, Stella P, et al. A phase II, open-label, randomized study to assess the efficacy and safety of AZD6244 (ARRY-142886) versus pemetrexed in patients with non-small cell lung cancer who have failed one or two prior chemotherapeutic regimens. J Thorac Oncol 2010;5:1630-6.
-
(2010)
J Thorac Oncol
, vol.5
, pp. 1630-1636
-
-
Hainsworth, J.D.1
Cebotaru, C.L.2
Kanarev, V.3
Ciuleanu, T.E.4
Damyanov, D.5
Stella, P.6
-
11
-
-
55749103404
-
Histone deacetylation: An attractive target for cancer therapy?
-
Al-Janadi A, Chandana SR, Conley BA. Histone deacetylation: an attractive target for cancer therapy? Drugs R D 2008;9:369-83.
-
(2008)
Drugs R D
, vol.9
, pp. 369-383
-
-
Al-Janadi, A.1
Chandana, S.R.2
Conley, B.A.3
-
12
-
-
43249120953
-
Histone deacetylase inhibitors: Mechanisms and clinical significance in cancer: HDAC inhibitor-induced apoptosis
-
Shankar S, Srivastava RK. Histone deacetylase inhibitors: mechanisms and clinical significance in cancer: HDAC inhibitor-induced apoptosis. Adv Exp Med Biol 2008;615:261-98.
-
(2008)
Adv Exp Med Biol
, vol.615
, pp. 261-298
-
-
Shankar, S.1
Srivastava, R.K.2
-
13
-
-
56949086914
-
HDAC inhibitors in leukemia: Current status and perspectives
-
Kouraklis G. HDAC inhibitors in leukemia: current status and perspectives. Leuk Res 2009;33:207-8.
-
(2009)
Leuk Res
, vol.33
, pp. 207-208
-
-
Kouraklis, G.1
-
14
-
-
68849110181
-
The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer
-
Crisanti MC, Wallace AF, Kapoor V, Vandermeers F, Dowling ML, Pereira LP, et al. The HDAC inhibitor panobinostat (LBH589) inhibits mesothelioma and lung cancer cells in vitro and in vivo with particular efficacy for small cell lung cancer. Mol Cancer Ther 2009;8:2221-31.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 2221-2231
-
-
Crisanti, M.C.1
Wallace, A.F.2
Kapoor, V.3
Vandermeers, F.4
Dowling, M.L.5
Pereira, L.P.6
-
15
-
-
51649092609
-
Vorinostat inhibits STAT6-mediated TH2 cytokine and TARC production and induces cell death in Hodgkin lymphoma cell lines
-
Buglio D, Georgakis GV, Hanabuchi S, Arima K, Khaskhely NM, Liu YJ, et al. Vorinostat inhibits STAT6-mediated TH2 cytokine and TARC production and induces cell death in Hodgkin lymphoma cell lines. Blood 2008;112:1424-33.
-
(2008)
Blood
, vol.112
, pp. 1424-1433
-
-
Buglio, D.1
Georgakis, G.V.2
Hanabuchi, S.3
Arima, K.4
Khaskhely, N.M.5
Liu, Y.J.6
-
16
-
-
38449087548
-
Differential response of p53 and p21 on HDAC inhibitor-mediated apoptosis in HCT116 colon cancer cells in vitro and in vivo
-
Zopf S, Neureiter D, Bouralexis S, Abt T, Glaser KB, Okamoto K, et al. Differential response of p53 and p21 on HDAC inhibitor-mediated apoptosis in HCT116 colon cancer cells in vitro and in vivo. Int J Oncol 2007;31:1391-402.
-
(2007)
Int J Oncol
, vol.31
, pp. 1391-1402
-
-
Zopf, S.1
Neureiter, D.2
Bouralexis, S.3
Abt, T.4
Glaser, K.B.5
Okamoto, K.6
-
17
-
-
43049092663
-
Phase II trial of oral vorinostat (suberoylanilide hydroxamic acid) in relapsed diffuse large-B-cell lymphoma
-
DOI 10.1093/annonc/mdn031
-
Crump M, Coiffier B, Jacobsen ED, Sun L, Ricker JL, Xie H, et al. Phase II trial of oral vorinostat (suberoylanilide hydroxamic acid) in relapsed diffuse large-B-cell lymphoma. Ann Oncol 2008;19:964-9. (Pubitemid 351627315)
-
(2008)
Annals of Oncology
, vol.19
, Issue.5
, pp. 964-969
-
-
Crump, M.1
Coiffier, B.2
Jacobsen, E.D.3
Sun, L.4
Ricker, J.L.5
Xie, H.6
Frankel, S.R.7
Randolph, S.S.8
Cheson, B.D.9
-
18
-
-
38449122336
-
The histone deacetylase inhibitors suberoylanilide hydroxamic (Vorinostat) and valproic acid induce irreversible and MDR1-independent resistance in human colon cancer cells
-
Fedier A, Dedes KJ, Imesch P, Von Bueren AO, Fink D. The histone deacetylase inhibitors suberoylanilide hydroxamic (Vorinostat) and valproic acid induce irreversible and MDR1-independent resistance in human colon cancer cells. Int J Oncol 2007;31:633-41.
-
(2007)
Int J Oncol
, vol.31
, pp. 633-641
-
-
Fedier, A.1
Dedes, K.J.2
Imesch, P.3
Von Bueren, A.O.4
Fink, D.5
-
19
-
-
60849106339
-
Vorinostat and bortezomib exert synergistic antiproliferative and proapoptotic effects in colon cancer cell models
-
Pitts TM, Morrow M, Kaufman SA, Tentler JJ, Eckhardt SG. Vorinostat and bortezomib exert synergistic antiproliferative and proapoptotic effects in colon cancer cell models. Mol Cancer Ther 2009;8:342-9.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 342-349
-
-
Pitts, T.M.1
Morrow, M.2
Kaufman, S.A.3
Tentler, J.J.4
Eckhardt, S.G.5
-
20
-
-
63549083115
-
ErbB-3 expression is associated with E-cadherin and their coexpression restores response to gefitinib in non-small-cell lung cancer (NSCLC)
-
Witta SE, Dziadziuszko R, Yoshida K, Hedman K, Varella-Garcia M, Bunn PA Jr, et al. ErbB-3 expression is associated with E-cadherin and their coexpression restores response to gefitinib in non-small-cell lung cancer (NSCLC). Ann Oncol 2009;20:689-95.
-
(2009)
Ann Oncol
, vol.20
, pp. 689-695
-
-
Witta, S.E.1
Dziadziuszko, R.2
Yoshida, K.3
Hedman, K.4
Varella-Garcia, M.5
Bunn Jr., P.A.6
-
21
-
-
36148950997
-
FDA approval summary: Vorinostat for treatment of advanced primary cutaneous T-cell lymphoma
-
DOI 10.1634/theoncologist.12-10-1247
-
Mann BS, Johnson JR, Cohen MH, Justice R, Pazdur R. FDA approval summary: vorinostat for treatment of advanced primary cutaneous Tcell lymphoma. Oncologist 2007;12:1247-52. (Pubitemid 350106355)
-
(2007)
Oncologist
, vol.12
, Issue.10
, pp. 1247-1252
-
-
Mann, B.S.1
Johnson, J.R.2
Cohen, M.H.3
Justice, R.4
Pazdur, R.5
-
22
-
-
58149242889
-
A phase II trial of vorinostat (suberoylanilide hydroxamic acid) in metastatic breast cancer: A California Cancer Consortium study
-
Luu TH, Morgan RJ, Leong L, McNamara M, Portnow J, Frankel P, et al. A phase II trial of vorinostat (suberoylanilide hydroxamic acid) in metastatic breast cancer: a California Cancer Consortium study. Clin Cancer Res 2008;14:7138-42.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 7138-7142
-
-
Luu, T.H.1
Morgan, R.J.2
Leong, L.3
McNamara, M.4
Portnow, J.5
Frankel, P.6
-
23
-
-
50249095068
-
Early phase II trial of oral vorinostat in relapsed or refractory breast, colorectal, or non-small cell lung cancer
-
Vansteenkiste J, Van Cutsem E, Dumez H, Chen C, Ricker JL, Randolph SS, et al. Early phase II trial of oral vorinostat in relapsed or refractory breast, colorectal, or non-small cell lung cancer. Invest New Drugs 2008;26:483-8.
-
(2008)
Invest New Drugs
, vol.26
, pp. 483-488
-
-
Vansteenkiste, J.1
Van Cutsem, E.2
Dumez, H.3
Chen, C.4
Ricker, J.L.5
Randolph, S.S.6
-
24
-
-
67649399669
-
Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: A Wisconsin Oncology Network phase II study
-
Traynor AM, Dubey S, Eickhoff JC, Kolesar JM, Schell K, Huie MS, et al. Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: a Wisconsin Oncology Network phase II study. J Thorac Oncol 2009;4:522-6.
-
(2009)
J Thorac Oncol
, vol.4
, pp. 522-526
-
-
Traynor, A.M.1
Dubey, S.2
Eickhoff, J.C.3
Kolesar, J.M.4
Schell, K.5
Huie, M.S.6
-
25
-
-
38149140216
-
Phase II trial of the histone deacetylase inhibitor vorinostat (Zolinza, suberoylanilide hydroxamic acid, SAHA) in patients with recurrent and/or metastatic head and neck cancer
-
Blumenschein GR Jr, Kies MS, Papadimitrakopoulou VA, Lu C, Kumar AJ, Ricker JL, et al. Phase II trial of the histone deacetylase inhibitor vorinostat (Zolinza, suberoylanilide hydroxamic acid, SAHA) in patients with recurrent and/or metastatic head and neck cancer. Invest New Drugs 2008;26:81-7.
-
(2008)
Invest New Drugs
, vol.26
, pp. 81-87
-
-
Blumenschein Jr., G.R.1
Kies, M.S.2
Papadimitrakopoulou, V.A.3
Lu, C.4
Kumar, A.J.5
Ricker, J.L.6
-
26
-
-
43049091153
-
A phase II study of vorinostat in the treatment of persistent or recurrent epithelial ovarian or primary peritoneal carcinoma: A Gynecologic Oncology Group study
-
Modesitt SC, Sill M, Hoffman JS, Bender DP. A phase II study of vorinostat in the treatment of persistent or recurrent epithelial ovarian or primary peritoneal carcinoma: a Gynecologic Oncology Group study. Gynecol Oncol 2008;109:182-6.
-
(2008)
Gynecol Oncol
, vol.109
, pp. 182-186
-
-
Modesitt, S.C.1
Sill, M.2
Hoffman, J.S.3
Bender, D.P.4
-
27
-
-
73949128107
-
Histone deacetylase inhibitors in cancer therapy
-
Lane AA, Chabner BA. Histone deacetylase inhibitors in cancer therapy. J Clin Oncol 2009;27:5459-68.
-
(2009)
J Clin Oncol
, vol.27
, pp. 5459-5468
-
-
Lane, A.A.1
Chabner, B.A.2
-
28
-
-
33947242973
-
Abrogation of MAPK and Akt signaling by AEE788 synergistically potentiates histone deacetylase inhibitor-induced apoptosis through reactive oxygen species generation
-
DOI 10.1158/1078-0432.CCR-06-1751
-
Yu C, Friday BB, Lai JP, McCollum A, Atadja P, Roberts LR, et al. Abrogation of MAPK and Akt signaling by AEE788 synergistically potentiates histone deacetylase inhibitor-induced apoptosis through reactive oxygen species generation. Clin Cancer Res 2007;13:1140-8. (Pubitemid 46424053)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.4
, pp. 1140-1148
-
-
Yu, C.1
Friday, B.B.2
Lai, J.-P.3
McCollum, A.4
Atadja, P.5
Roberts, L.R.6
Adjei, A.A.7
-
29
-
-
26944440597
-
Synergistic interactions between MEK1/2 and histone deacetylase inhibitors in BCR/ABL+ human leukemia cells
-
DOI 10.1038/sj.leu.2403868, PII 2403868
-
Yu C, Dasmahapatra G, Dent P, Grant S. Synergistic interactions between MEK1/2 and histone deacetylase inhibitors in BCR/ABL+ human leukemia cells. Leukemia 2005;19:1579-89. (Pubitemid 43090402)
-
(2005)
Leukemia
, vol.19
, Issue.9
, pp. 1579-1589
-
-
Yu, C.1
Dasmahapatra, G.2
Dent, P.3
Grant, S.4
-
30
-
-
67650498443
-
Growth-inhibitory and antiangiogenic activity of the MEK inhibitor PD0325901 in malignant melanoma with or without BRAF mutations
-
Ciuffreda L, Del Bufalo D, Desideri M, Di Sanza C, Stoppacciaro A, Ricciardi MR, et al. Growth-inhibitory and antiangiogenic activity of the MEK inhibitor PD0325901 in malignant melanoma with or without BRAF mutations. Neoplasia 2009;11:720-31.
-
(2009)
Neoplasia
, vol.11
, pp. 720-731
-
-
Ciuffreda, L.1
Del Bufalo, D.2
Desideri, M.3
Di Sanza, C.4
Stoppacciaro, A.5
Ricciardi, M.R.6
-
31
-
-
78650465237
-
Identification of predictive markers of response to the MEK1/2 inhibitor selumetinib (AZD6244) in KRAS-mutated colorectal cancer
-
Tentler JJ, Nallapareddy S, Tan AC, Spreafico A, Pitts TM, Morelli MP, et al. Identification of predictive markers of response to the MEK1/2 inhibitor selumetinib (AZD6244) in KRAS-mutated colorectal cancer. Mol Cancer Ther 2010;9:3351-62.
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 3351-3362
-
-
Tentler, J.J.1
Nallapareddy, S.2
Tan, A.C.3
Spreafico, A.4
Pitts, T.M.5
Morelli, M.P.6
-
32
-
-
33745590870
-
Anti-tumor activity of the combination of cetuximab, an anti-EGFR blocking monoclonal antibody and ZD6474, an inhibitor of VEGFR and EGFR tyrosine kinases
-
DOI 10.1002/jcp.20666
-
Morelli MP, Cascone T, Troiani T, Tuccillo C, Bianco R, Normanno N, et al. Anti-tumor activity of the combination of cetuximab, an anti-EGFR blocking monoclonal antibody and ZD6474, an inhibitor of VEGFR and EGFR tyrosine kinases. J Cell Physiol 2006;208:344-53. (Pubitemid 43993425)
-
(2006)
Journal of Cellular Physiology
, vol.208
, Issue.2
, pp. 344-353
-
-
Morelli, M.P.1
Cascone, T.2
Troiani, T.3
Tuccillo, C.4
Bianco, R.5
Normanno, N.6
Romano, M.7
Veneziani, B.M.8
Fontanini, G.9
Eckhardt, S.G.10
De Pacido, S.11
Tortora, G.12
Ciardiello, F.13
-
33
-
-
66149180567
-
Abnormalities in glucose uptake and metabolism in imatinib-resistant human BCR-ABL-positive cells
-
Kominsky DJ, Klawitter J, Brown JL, Klawitter J, Christians U, Leibfritz D, et al. Abnormalities in glucose uptake and metabolism in imatinib-resistant human BCR-ABL-positive cells. Clin Cancer Res 2009;15:3442-50.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 3442-3450
-
-
Kominsky, D.J.1
Klawitter, J.2
Brown, J.L.3
Klawitter, J.4
Christians, U.5
Leibfritz, D.6
-
35
-
-
26444469502
-
Detection of resistance to imatinib by metabolic profiling: Clinical and drug development implications
-
DOI 10.2165/00129785-200505050-00002
-
Serkova N, Boros LG. Detection of resistance to imatinib by metabolic profiling: clinical and drug development implications. Am J Pharmacogenomics 2005;5:293-302. (Pubitemid 41425607)
-
(2005)
American Journal of PharmacoGenomics
, vol.5
, Issue.5
, pp. 293-302
-
-
Serkova, N.1
Boros, L.G.2
-
36
-
-
38949096781
-
Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes
-
DOI 10.1182/blood-2007-06-098061
-
Garcia-Manero G, Yang H, Bueso-Ramos C, Ferrajoli A, Cortes J, Wierda WG, et al. Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes. Blood 2008;111:1060-6. (Pubitemid 351213383)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1060-1066
-
-
Garcia-Manero, G.1
Yang, H.2
Bueso-Ramos, C.3
Ferrajoli, A.4
Cortes, J.5
Wierda, W.G.6
Faderl, S.7
Koller, C.8
Morris, G.9
Rosner, G.10
Loboda, A.11
Fantin, V.R.12
Randolph, S.S.13
Hardwick, J.S.14
Reilly, J.F.15
Chen, C.16
Ricker, J.L.17
Secrist, J.P.18
Richon, V.M.19
Frankel, S.R.20
Kantarjian, H.M.21
more..
-
37
-
-
39749103428
-
Phase I trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) in patients with advanced multiple myeloma
-
DOI 10.1080/10428190701817258, PII 790280844
-
Richardson P, Mitsiades C, Colson K, Reilly E, McBride L, Chiao J, et al. Phase I trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) in patients with advanced multiple myeloma. Leuk Lymphoma 2008;49:502-7. (Pubitemid 351298334)
-
(2008)
Leukemia and Lymphoma
, vol.49
, Issue.3
, pp. 502-507
-
-
Richardson, P.1
Mitsiades, C.2
Colson, K.3
Reilly, E.4
McBride, L.5
Chiao, J.6
Sun, L.7
Ricker, J.8
Rizvi, S.9
Oerth, C.10
Atkins, B.11
Fearen, I.12
Anderson, K.13
Siegel, D.14
-
38
-
-
73649124286
-
Extracellular signal-regulated kinase signaling pathway regulates breast cancer cell migration by maintaining slug expression
-
Chen H, Zhu G, Li Y, Padia RN, Dong Z, Pan ZK, et al. Extracellular signal-regulated kinase signaling pathway regulates breast cancer cell migration by maintaining slug expression. Cancer Res 2009;69:9228-35.
-
(2009)
Cancer Res
, vol.69
, pp. 9228-9235
-
-
Chen, H.1
Zhu, G.2
Li, Y.3
Padia, R.N.4
Dong, Z.5
Pan, Z.K.6
-
39
-
-
39449133669
-
Regulation of cancer cell survival, migration, and invasion by twist: AKT2 comes to interplay
-
DOI 10.1158/0008-5472.CAN-07-5067
-
Cheng GZ, Zhang W, Wang LH. Regulation of cancer cell survival, migration, and invasion by Twist: AKT2 comes to interplay. Cancer Res 2008;68:957-60. (Pubitemid 351272210)
-
(2008)
Cancer Research
, vol.68
, Issue.4
, pp. 957-960
-
-
Cheng, G.Z.1
Zhang, W.2
Wang, L.-H.3
-
40
-
-
33744927684
-
2-terminal kinase/activator protein-1 signaling to regulate cell migration
-
DOI 10.1158/0008-5472.CAN-05-2858
-
Cui X, Kim HJ, Kuiatse I, Kim H, Brown PH, Lee AV. Epidermal growth factor induces insulin receptor substrate-2 in breast cancer cells via c-Jun NH(2)-terminal kinase/activator protein-1 signaling to regulate cell migration. Cancer Res 2006;66:5304-13. (Pubitemid 43844955)
-
(2006)
Cancer Research
, vol.66
, Issue.10
, pp. 5304-5313
-
-
Cui, X.1
Kim, H.-J.2
Kuiatse, I.3
Kim, H.4
Brown, P.H.5
Lee, A.V.6
-
41
-
-
0033231070
-
Epidermal growth factor promotes MDA-MB-231 breast cancer cell migration through a phosphatidylinositol 3'-kinase and phospholipase C-dependent mechanism
-
Price JT, Tiganis T, Agarwal A, Djakiew D, Thompson EW. Epidermal growth factor promotes MDA-MB-231 breast cancer cell migration through a phosphatidylinositol 30-kinase and phospholipase C-dependent mechanism. Cancer Res 1999;59:5475-8. (Pubitemid 29526460)
-
(1999)
Cancer Research
, vol.59
, Issue.21
, pp. 5475-5478
-
-
Price, J.T.1
Tiganis, T.2
Agarwal, A.3
Djakiew, D.4
Thompson, E.W.5
-
42
-
-
0035393583
-
Epithelial cancer cell migration: A role for chemokine receptors?
-
Scotton CJ, Wilson JL, Milliken D, Stamp G, Balkwill FR. Epithelial cancer cell migration: a role for chemokine receptors? Cancer Res 2001;61:4961-5. (Pubitemid 32681518)
-
(2001)
Cancer Research
, vol.61
, Issue.13
, pp. 4961-4965
-
-
Scotton, C.J.1
Wilson, J.L.2
Milliken, D.3
Stamp, G.4
Balkwill, F.R.5
-
43
-
-
0035866387
-
Up-regulation of vascular endothelial growth factor in breast cancer cells by the heregulin-beta1-activated p38 signaling pathway enhances endothelial cell migration
-
Xiong S, Grijalva R, Zhang L, Nguyen NT, Pisters PW, Pollock RE, et al. Up-regulation of vascular endothelial growth factor in breast cancer cells by the heregulin-beta1-activated p38 signaling pathway enhances endothelial cell migration. Cancer Res 2001;61:1727-32. (Pubitemid 34292611)
-
(2001)
Cancer Research
, vol.61
, Issue.4
, pp. 1727-1732
-
-
Xiong, S.1
Grijalva, R.2
Zhang, L.3
Nguyen, N.T.4
Pisters, P.W.5
Pollock, R.E.6
Yu, D.7
-
44
-
-
70349495869
-
Targeting vascular endothelial growth factor receptor-1 and -3 with cediranib (AZD2171): Effects on migration and invasion of gastrointestinal cancer cell lines
-
Morelli MP, Brown AM, Pitts TM, Tentler JJ, Ciardiello F, Ryan A, et al. Targeting vascular endothelial growth factor receptor-1 and -3 with cediranib (AZD2171): effects on migration and invasion of gastrointestinal cancer cell lines. Mol Cancer Ther 2009;8:2546-58.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 2546-2558
-
-
Morelli, M.P.1
Brown, A.M.2
Pitts, T.M.3
Tentler, J.J.4
Ciardiello, F.5
Ryan, A.6
-
45
-
-
36749096778
-
Targeted agents to improve treatment results in colon cancer: Bevacizumab and cetuximab
-
Klein B, Gottfried M. Targeted agents to improve treatment results in colon cancer: bevacizumab and cetuximab. JBUON2007;12(Suppl 1):S127-36. (Pubitemid 350200871)
-
(2007)
Journal of B.U.ON.
, vol.12
, Issue.SUPPL. 1
-
-
Klein, B.1
Gottfried, M.2
-
46
-
-
40849147041
-
EGFR antagonists in cancer treatment
-
Ciardiello F, Tortora G. EGFR antagonists in cancer treatment. N Engl J Med 2008;358:1160-74.
-
(2008)
N Engl J Med
, vol.358
, pp. 1160-1174
-
-
Ciardiello, F.1
Tortora, G.2
-
47
-
-
34047132314
-
Combination of EGFR gene copy number and protein expression predicts outcome for advanced non-small-cell lung cancer patients treated with gefitinib
-
DOI 10.1093/annonc/mdm003
-
Hirsch FR, Varella-Garcia M, Cappuzzo F, McCoy J, Bemis L, Xavier AC, et al. Combination of EGFR gene copy number and protein expression predicts outcome for advanced non-small-cell lung cancer patients treated with gefitinib. Ann Oncol 2007;18:752-60. (Pubitemid 46523281)
-
(2007)
Annals of Oncology
, vol.18
, Issue.4
, pp. 752-760
-
-
Hirsch, F.R.1
Varella-Garcia, M.2
Cappuzzo, F.3
McCoy, J.4
Bemis, L.5
Xavier, A.C.6
Dziadziuszko, R.7
Gumerlock, P.8
Chansky, K.9
West, H.10
Gazdar, A.F.11
Crino, L.12
Gandara, D.R.13
Franklin, W.A.14
Bunn Jr., P.A.15
-
48
-
-
70449533764
-
Effects of matrine against the growth of human lung cancer and hepatoma cells as well as lung cancer cell migration
-
Zhang Y, Zhang H, Yu P, Liu Q, Liu K, Duan H, et al. Effects of matrine against the growth of human lung cancer and hepatoma cells as well as lung cancer cell migration. Cytotechnology 2009;59:191-200.
-
(2009)
Cytotechnology
, vol.59
, pp. 191-200
-
-
Zhang, Y.1
Zhang, H.2
Yu, P.3
Liu, Q.4
Liu, K.5
Duan, H.6
-
49
-
-
73349094741
-
Analysis of PTEN, BRAF, and EGFR status in determining benefit from cetuximab therapy in wild-type KRAS metastatic colon cancer
-
Laurent-Puig P, Cayre A, Manceau G, Buc E, Bachet JB, Lecomte T, et al. Analysis of PTEN, BRAF, and EGFR status in determining benefit from cetuximab therapy in wild-type KRAS metastatic colon cancer. J Clin Oncol 2009;27:5924-30.
-
(2009)
J Clin Oncol
, vol.27
, pp. 5924-5930
-
-
Laurent-Puig, P.1
Cayre, A.2
Manceau, G.3
Buc, E.4
Bachet, J.B.5
Lecomte, T.6
-
50
-
-
46349092797
-
Primary resistance to cetuximab therapy in EGFR FISH-positive colorectal cancer patients
-
DOI 10.1038/sj.bjc.6604439, PII 6604439
-
Cappuzzo F, Varella-Garcia M, Finocchiaro G, Skokan M, Gajapathy S, Carnaghi C, et al. Primary resistance to cetuximab therapy in EGFR FISH-positive colorectal cancer patients. Br J Cancer 2008;99:83-9. (Pubitemid 351920237)
-
(2008)
British Journal of Cancer
, vol.99
, Issue.1
, pp. 83-89
-
-
Cappuzzo, F.1
Varella-Garcia, M.2
Finocchiaro, G.3
Skokan, M.4
Gajapathy, S.5
Carnaghi, C.6
Rimassa, L.7
Rossi, E.8
Ligorio, C.9
Di, T.L.10
Holmes, A.J.11
Toschi, L.12
Tallini, G.13
Destro, A.14
Roncalli, M.15
Santoro, A.16
Janne, P.A.17
-
51
-
-
61449154484
-
KRAS mutations and sensitivity to epidermal growth factor receptor inhibitors in colorectal cancer: Practical application of patient selection
-
Jimeno A, Messersmith WA, Hirsch FR, Franklin WA, Eckhardt SG. KRAS mutations and sensitivity to epidermal growth factor receptor inhibitors in colorectal cancer: practical application of patient selection. J Clin Oncol 2009;27:1130-6.
-
(2009)
J Clin Oncol
, vol.27
, pp. 1130-1136
-
-
Jimeno, A.1
Messersmith, W.A.2
Hirsch, F.R.3
Franklin, W.A.4
Eckhardt, S.G.5
-
52
-
-
18644378618
-
A role for K-ras in conferring resistance to the MEK inhibitor, CI-1040
-
DOI 10.1593/neo.04532
-
Wang Y, Van Becelaere K, Jiang P, Przybranowski S, Omer C, Sebolt-Leopold J. A role for KRAS in conferring resistance to the MEK inhibitor, CI-1040. Neoplasia 2005;7:336-47. (Pubitemid 40664223)
-
(2005)
Neoplasia
, vol.7
, Issue.4
, pp. 336-347
-
-
Wang, Y.1
Van Becelaere, K.2
Jiang, P.3
Przybranowski, S.4
Omer, C.5
Sebolt-Leopold, J.6
-
53
-
-
77950261074
-
Transcriptional pathway signatures predict MEK addiction and response to selumetinib (AZD6244)
-
Dry JR, Pavey S, Pratilas CA, Harbron C, Runswick S, Hodgson D, et al. Transcriptional pathway signatures predict MEK addiction and response to selumetinib (AZD6244). Cancer Res 2010;70:2264-73.
-
(2010)
Cancer Res
, vol.70
, pp. 2264-2273
-
-
Dry, J.R.1
Pavey, S.2
Pratilas, C.A.3
Harbron, C.4
Runswick, S.5
Hodgson, D.6
-
54
-
-
33947401129
-
Biological characterization of ARRY-142886 (AZD6244), a potent, highly selective mitogen-activated protein kinase kinase 1/2 inhibitor
-
DOI 10.1158/1078-0432.CCR-06-1150
-
Yeh TC, Marsh V, Bernat BA, Ballard J, Colwell H, Evans RJ, et al. Biological characterization of ARRY-142886 (AZD6244), a potent, highly selective mitogen-activated protein kinase kinase 1/2 inhibitor. Clin Cancer Res 2007;13:1576-83. (Pubitemid 46450450)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.5
, pp. 1576-1583
-
-
Yeh, T.C.1
Marsh, V.2
Bernat, B.A.3
Ballard, J.4
Colwell, H.5
Evans, R.J.6
Parry, J.7
Smith, D.8
Brandhuber, B.J.9
Gross, S.10
Marlow, A.11
Hurley, B.12
Lyssikatos, J.13
Lee, P.A.14
Winkler, J.D.15
Koch, K.16
Wallace, E.17
-
55
-
-
31544452076
-
Restoring E-cadherin expression increases sensitivity to epidermal growth factor receptor inhibitors in lung cancer cell lines
-
DOI 10.1158/0008-5472.CAN-05-1988
-
Witta SE, Gemmill RM, Hirsch FR, Coldren CD, Hedman K, Ravdel L, et al. Restoring E-cadherin expression increases sensitivity to epidermal growth factor receptor inhibitors in lung cancer cell lines. Cancer Res 2006;66:944-50. (Pubitemid 43165962)
-
(2006)
Cancer Research
, vol.66
, Issue.2
, pp. 944-950
-
-
Witta, S.E.1
Gemmill, R.M.2
Hirsch, F.R.3
Coldren, C.D.4
Hedman, K.5
Ravdel, L.6
Helfrich, B.7
Dziadziuszko, R.8
Chan, D.C.9
Sugita, M.10
Chan, Z.11
Baron, A.12
Franklin, W.13
Drabkin, H.A.14
Girard, L.15
Gazdar, A.F.16
Minna, J.D.17
Bunn Jr., P.A.18
-
56
-
-
33750571170
-
Heterodimerization of insulin-like growth factor receptor/epidermal growth factor receptor and induction of survivin expression counteract the antitumor action of erlotinib
-
DOI 10.1158/0008-5472.CAN-06-1684
-
Morgillo F, Woo JK, Kim ES, Hong WK, Lee HY. Heterodimerization of insulin-like growth factor receptor/epidermal growth factor receptor and induction of survivin expression counteract the antitumor action of erlotinib. Cancer Res 2006;66:10100-11. (Pubitemid 44672064)
-
(2006)
Cancer Research
, vol.66
, Issue.20
, pp. 10100-10111
-
-
Morgillo, F.1
Woo, J.K.2
Kim, E.S.3
Hong, W.K.4
Lee, H.-Y.5
-
57
-
-
31844453715
-
Signalling responses linked to betulinic acid-induced apoptosis are antagonized by MEK inhibitor U0126 in adherent or 3D spheroid melanoma irrespective of p53 status
-
DOI 10.1002/ijc.21478
-
Rieber M, Rieber MS. Signalling responses linked to betulinic acid-induced apoptosis are antagonized by MEK inhibitor U0126 in adherent or 3D spheroid melanoma irrespective of p53 status. Int J Cancer 2006;118:1135-43. (Pubitemid 43185599)
-
(2006)
International Journal of Cancer
, vol.118
, Issue.5
, pp. 1135-1143
-
-
Rieber, M.1
Rieber, M.S.2
|