-
1
-
-
0035902180
-
Oncogenic kinase signalling
-
Blume-Jensen P, Hunter T. Oncogenic kinase signalling. Nature 2001;411:355-65.
-
(2001)
Nature
, vol.411
, pp. 355-365
-
-
Blume-Jensen, P.1
Hunter, T.2
-
2
-
-
21244500970
-
Therapeutic targeting of receptor tyrosine kinases in lung cancer
-
Choong NW, Ma PC, Salgia R. Therapeutic targeting of receptor tyrosine kinases in lung cancer. Expert Opin Ther Targets 2005;9:533-59.
-
(2005)
Expert Opin Ther Targets
, vol.9
, pp. 533-559
-
-
Choong, N.W.1
Ma, P.C.2
Salgia, R.3
-
3
-
-
0032541677
-
Tyrosine kinase receptor-activated signal transduction pathways which lead to oncogenesis
-
Porter AC, Vaillancourt RR. Tyrosine kinase receptor-activated signal transduction pathways which lead to oncogenesis. Oncogene 1998;17:1343-52.
-
(1998)
Oncogene
, vol.17
, pp. 1343-1352
-
-
Porter, A.C.1
Vaillancourt, R.R.2
-
4
-
-
0034213931
-
RTK mutations and human syndromes: When good receptors turn bad
-
Robertson SC, Tynan J, Donoghue DJ. RTK mutations and human syndromes: when good receptors turn bad. Trends Genet 2000;16:368.
-
(2000)
Trends Genet
, vol.16
, pp. 368
-
-
Robertson, S.C.1
Tynan, J.2
Donoghue, D.J.3
-
5
-
-
0024376173
-
-
Bos JL. ras oncogenes in human cancer: a review. Cancer Res 1989;49:4682-9.
-
Bos JL. ras oncogenes in human cancer: a review. Cancer Res 1989;49:4682-9.
-
-
-
-
7
-
-
1342299898
-
Mutation analysis of the BRAF, ARAF, and RAF-1 genes in human colorectal adenocarcinomas
-
Fransen K, Klintenas M, Osterstrom A, Dimberg J, Monstein HJ, Soderkvist P. Mutation analysis of the BRAF, ARAF, and RAF-1 genes in human colorectal adenocarcinomas. Carcinogenesis 2004;25:527-33.
-
(2004)
Carcinogenesis
, vol.25
, pp. 527-533
-
-
Fransen, K.1
Klintenas, M.2
Osterstrom, A.3
Dimberg, J.4
Monstein, H.J.5
Soderkvist, P.6
-
8
-
-
28844509531
-
K-ras as a target for cancer therapy
-
Friday BB, Adjei AA. K-ras as a target for cancer therapy. Biochim Biophys Acta 2005;1756:127-44.
-
(2005)
Biochim Biophys Acta
, vol.1756
, pp. 127-144
-
-
Friday, B.B.1
Adjei, A.A.2
-
9
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, et al. Mutations of the BRAF gene in human cancer. Nature 2002;417: 949-54.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
10
-
-
27544453376
-
Mutations of C-RAF are rare in human cancer because C-RAF has a low basal kinase activity compared with B-RAF
-
Emuss V, Garnett M, Mason C, Marais R. Mutations of C-RAF are rare in human cancer because C-RAF has a low basal kinase activity compared with B-RAF. Cancer Res 2005;65:9719-26.
-
(2005)
Cancer Res
, vol.65
, pp. 9719-9726
-
-
Emuss, V.1
Garnett, M.2
Mason, C.3
Marais, R.4
-
11
-
-
20044376685
-
Mutational analysis of the ARAF gene in human cancers
-
Lee JW, Soung YH, Kim SY, et al. Mutational analysis of the ARAF gene in human cancers. APMIS 2005; 113:54-7.
-
(2005)
APMIS
, vol.113
, pp. 54-57
-
-
Lee, J.W.1
Soung, Y.H.2
Kim, S.Y.3
-
12
-
-
27244457769
-
Raf: A strategic target for therapeutic development against cancer
-
Beeram M, Patnaik A, Rowinsky EK. Raf: a strategic target for therapeutic development against cancer. J Clin Oncol 2005;23:6771-90.
-
(2005)
J Clin Oncol
, vol.23
, pp. 6771-6790
-
-
Beeram, M.1
Patnaik, A.2
Rowinsky, E.K.3
-
13
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan PT, Garnett MJ, Roe SM, et al. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 2004;116:855-67.
-
(2004)
Cell
, vol.116
, pp. 855-867
-
-
Wan, P.T.1
Garnett, M.J.2
Roe, S.M.3
-
14
-
-
0033590636
-
Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors
-
Hoshino R, Chatani Y, Yamori T, et al. Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors. Oncogene 1999;18:813-22.
-
(1999)
Oncogene
, vol.18
, pp. 813-822
-
-
Hoshino, R.1
Chatani, Y.2
Yamori, T.3
-
15
-
-
14844285975
-
Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-small-cell lung, breast, colon, and pancreatic cancer
-
Rinehart J, Adjei AA, Lorusso PM, et al. Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-small-cell lung, breast, colon, and pancreatic cancer. J Clin Oncol 2004;22: 4456-62.
-
(2004)
J Clin Oncol
, vol.22
, pp. 4456-4462
-
-
Rinehart, J.1
Adjei, A.A.2
Lorusso, P.M.3
-
16
-
-
31544450194
-
A Phase 1-2 clinical study of a second generation oral MEK inhibitor, PD 0325901 in patients with advanced cancer [abstract]
-
Orlando, FL
-
Lorusso P, Krishnamurthi S, Rinehart J, et al. A Phase 1-2 clinical study of a second generation oral MEK inhibitor, PD 0325901 in patients with advanced cancer [abstract]. Proceedings of the American Society of Clinical Oncology Annual Meeting; 2005; Orlando, FL.
-
(2005)
Proceedings of the American Society of Clinical Oncology Annual Meeting
-
-
Lorusso, P.1
Krishnamurthi, S.2
Rinehart, J.3
-
17
-
-
33947389951
-
-
Chow L, Eckhardt S, Reid J, et al. A first in human dose-ranging study to assess the pharmacokinetics, pharmacodynamics, and toxicities of the Mek inhibitor, ARRY-142886 (AZD6244), in patients with advanced solid malignancies [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2005; Philadelphia, PA.
-
Chow L, Eckhardt S, Reid J, et al. A first in human dose-ranging study to assess the pharmacokinetics, pharmacodynamics, and toxicities of the Mek inhibitor, ARRY-142886 (AZD6244), in patients with advanced solid malignancies [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2005; Philadelphia, PA.
-
-
-
-
18
-
-
0029955970
-
Interdependent domains controlling the enzymatic activity of mitogen-activated protein kinase kinase 1
-
Mansour SJ, Candia JM, Matsuura JE, Manning MC, Ahn NG. Interdependent domains controlling the enzymatic activity of mitogen-activated protein kinase kinase 1. Biochemistry 1996;35:15529-36.
-
(1996)
Biochemistry
, vol.35
, pp. 15529-15536
-
-
Mansour, S.J.1
Candia, J.M.2
Matsuura, J.E.3
Manning, M.C.4
Ahn, N.G.5
-
20
-
-
23944439944
-
Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies
-
Lorusso PM, Adjei AA, Varterasian M, et al. Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies. J Clin Oncol 2005;23:5281-93.
-
(2005)
J Clin Oncol
, vol.23
, pp. 5281-5293
-
-
Lorusso, P.M.1
Adjei, A.A.2
Varterasian, M.3
-
21
-
-
15744380263
-
Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
-
Ohren JF, Chen H, Pavlovsky A, et al. Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat Struct Mol Biol 2004;11:1192-7.
-
(2004)
Nat Struct Mol Biol
, vol.11
, pp. 1192-1197
-
-
Ohren, J.F.1
Chen, H.2
Pavlovsky, A.3
-
23
-
-
0037022666
-
Apoptosis and melanogenesis in human melanoma cells induced by anthrax lethal factor inactivation of mitogen-activated protein kinase kinase
-
Koo HM, VanBrocklin M, McWilliams MJ, Leppla SH, Duesbery NS, Woude GF. Apoptosis and melanogenesis in human melanoma cells induced by anthrax lethal factor inactivation of mitogen-activated protein kinase kinase. Proc Natl Acad Sci U S A 2002;99: 3052-7.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 3052-3057
-
-
Koo, H.M.1
VanBrocklin, M.2
McWilliams, M.J.3
Leppla, S.H.4
Duesbery, N.S.5
Woude, G.F.6
-
24
-
-
16444378374
-
Inactivation of the mitogen-activated protein kinase pathway as a potential target-based therapy in ovarian serous tumors with KRAS or BRAF mutations
-
Pohl G, Ho CL, Kurman RJ, Bristow R, Wang TL, Shih IM. Inactivation of the mitogen-activated protein kinase pathway as a potential target-based therapy in ovarian serous tumors with KRAS or BRAF mutations. Cancer Res 2005;65:1994-2000.
-
(2005)
Cancer Res
, vol.65
, pp. 1994-2000
-
-
Pohl, G.1
Ho, C.L.2
Kurman, R.J.3
Bristow, R.4
Wang, T.L.5
Shih, I.M.6
-
25
-
-
31144453233
-
BRAF mutation predicts sensitivity to MEK inhibition
-
Solit DB, Garraway LA, Pratilas CA, et al. BRAF mutation predicts sensitivity to MEK inhibition. Nature 2005;439:358-62.
-
(2005)
Nature
, vol.439
, pp. 358-362
-
-
Solit, D.B.1
Garraway, L.A.2
Pratilas, C.A.3
-
26
-
-
7444245100
-
Renewing the conspiracy theory debate: Does Raf function alone to mediate Ras oncogenesis?
-
Repasky GA, Chenette EJ, Der CJ. Renewing the conspiracy theory debate: does Raf function alone to mediate Ras oncogenesis? Trends Cell Biol 2004;14: 639-47.
-
(2004)
Trends Cell Biol
, vol.14
, pp. 639-647
-
-
Repasky, G.A.1
Chenette, E.J.2
Der, C.J.3
-
27
-
-
0034881019
-
Molecular mechanisms mediating mammalian mitogen-activated protein kinase (MAPK) kinase (MEK)-MAPK cell survival signals
-
Ballif BA, Blenis J. Molecular mechanisms mediating mammalian mitogen-activated protein kinase (MAPK) kinase (MEK)-MAPK cell survival signals. Cell Growth Differ 2001;12:397-408.
-
(2001)
Cell Growth Differ
, vol.12
, pp. 397-408
-
-
Ballif, B.A.1
Blenis, J.2
-
28
-
-
0036061374
-
Inhibitors of farnesyl protein transferase and MEK1,2 induce apoptosis in fibroblasts transformed with farnesylated but not geranylgeranylated H-Ras
-
Brassard DL, English JM, Malkowski M, Kirschmeier P, Nagabhushan TL, Bishop WR. Inhibitors of farnesyl protein transferase and MEK1,2 induce apoptosis in fibroblasts transformed with farnesylated but not geranylgeranylated H-Ras. Exp Cell Res 2002;273: 138-46.
-
(2002)
Exp Cell Res
, vol.273
, pp. 138-146
-
-
Brassard, D.L.1
English, J.M.2
Malkowski, M.3
Kirschmeier, P.4
Nagabhushan, T.L.5
Bishop, W.R.6
-
29
-
-
0035951784
-
1 cell cycle arrest and apoptosis in tumor cells in which the pathway is constitutively activated: Up-regulation of p27(Kip1)
-
1 cell cycle arrest and apoptosis in tumor cells in which the pathway is constitutively activated: up-regulation of p27(Kip1). J Biol Chem 2001;276:2686-92.
-
(2001)
J Biol Chem
, vol.276
, pp. 2686-2692
-
-
Hoshino, R.1
Tanimura, S.2
Watanabe, K.3
Kataoka, T.4
Kohno, M.5
-
30
-
-
0034823632
-
Therapeutic targeting of the MEK/MAPK signal transduction module in acute myeloid leukemia
-
Milella M, Kornblau SM, Estrov Z, et al. Therapeutic targeting of the MEK/MAPK signal transduction module in acute myeloid leukemia. J Clin Invest 2001;108:851-9.
-
(2001)
J Clin Invest
, vol.108
, pp. 851-859
-
-
Milella, M.1
Kornblau, S.M.2
Estrov, Z.3
-
31
-
-
0035313981
-
The MEK1-ERK map kinase pathway and the PI 3-kinase-Akt pathway independently mediate anti-apoptotic signals in HepG2 liver cancer cells
-
Mitsui H, Takuwa N, Maruyama T, et al. The MEK1-ERK map kinase pathway and the PI 3-kinase-Akt pathway independently mediate anti-apoptotic signals in HepG2 liver cancer cells. Int J Cancer 2001; 92:55-62.
-
(2001)
Int J Cancer
, vol.92
, pp. 55-62
-
-
Mitsui, H.1
Takuwa, N.2
Maruyama, T.3
-
32
-
-
0032984348
-
Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo
-
Sebolt-Leopold JS, Dudley DT, Herrera R, et al. Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo. Nat Med 1999;5: 810-6.
-
(1999)
Nat Med
, vol.5
, pp. 810-816
-
-
Sebolt-Leopold, J.S.1
Dudley, D.T.2
Herrera, R.3
-
33
-
-
33947355358
-
Anti-tumor activity, pharmacokinetic and pharmacodynamic effects of the MEK inhibitor ARRY-142886 (AZD6244) in a BxPC3 pancreatic tumor xenograft model [abstract]
-
Geneva, Switzerland
-
Winkler J, Lee P, Wallace E, et al. Anti-tumor activity, pharmacokinetic and pharmacodynamic effects of the MEK inhibitor ARRY-142886 (AZD6244) in a BxPC3 pancreatic tumor xenograft model [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2004; Geneva, Switzerland.
-
(2004)
Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics
-
-
Winkler, J.1
Lee, P.2
Wallace, E.3
-
34
-
-
33947409094
-
ARRY-142886, a potent and selective MEK Inhibitor: III) Efficacy Against Human Xenograft Models Correlates with Decreased ERK phosphorylation [abstract]
-
Orlando, FL
-
Lee P, Wallace E, Yeh T, et al. ARRY-142886, a potent and selective MEK Inhibitor: III) Efficacy Against Human Xenograft Models Correlates with Decreased ERK phosphorylation [abstract]. Proceedings of the 95th Annual AACR Meeting; 2004; Orlando, FL.
-
(2004)
Proceedings of the 95th Annual AACR Meeting
-
-
Lee, P.1
Wallace, E.2
Yeh, T.3
-
35
-
-
33947390386
-
4-(4-Bromo-2-fluorophenylamino)- 1-methyl-pyridin-2(1H)ones: Potent and selective MEK 1,2 inhibitors [abstract]
-
Philadelphia, PA
-
Wallace E, Lyssikatos J, Blake J, et al. 4-(4-Bromo-2-fluorophenylamino)- 1-methyl-pyridin-2(1H)ones: potent and selective MEK 1,2 inhibitors [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2005; Philadelphia, PA.
-
(2005)
Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics
-
-
Wallace, E.1
Lyssikatos, J.2
Blake, J.3
-
36
-
-
33947416100
-
-
Lee P, Wallace E, Yeh T, et al. Demonstration of broad in vivo anti-tumor activity of ARRY-142886 (AZD6244), a potent and selective MEK inhibitor [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2004; Geneva, Switzerland.
-
Lee P, Wallace E, Yeh T, et al. Demonstration of broad in vivo anti-tumor activity of ARRY-142886 (AZD6244), a potent and selective MEK inhibitor [abstract]. Proceedings of the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; 2004; Geneva, Switzerland.
-
-
-
|