-
1
-
-
84864258996
-
A landscape of driver mutations in melanoma
-
Hodis E, Watson IR, Kryukov GV, Arold ST, Imielinski M, Theurillat JP, et al. A landscape of driver mutations in melanoma. Cell 2012; 150: 251-63.
-
(2012)
Cell
, vol.150
, pp. 251-263
-
-
Hodis, E.1
Watson, I.R.2
Kryukov, G.V.3
Arold, S.T.4
Imielinski, M.5
Theurillat, J.P.6
-
2
-
-
84897018336
-
The molecular pathology of melanoma: An integrated taxonomy of melanocytic neoplasia
-
Bastian BC. The molecular pathology of melanoma: an integrated taxonomy of melanocytic neoplasia. Annu Rev Pathol 2014; 9: 239-71.
-
(2014)
Annu Rev Pathol
, vol.9
, pp. 239-271
-
-
Bastian, B.C.1
-
3
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, Stephens P, Edkins S, Clegg S, 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
Stephens, P.4
Edkins, S.5
Clegg, S.6
-
4
-
-
84896714827
-
Safety and efficacy of vemurafanib in BRAF(V600E) and BRAF(V600K) mutation-positive melanoma (BRIM-3): Extended follow-up of a phase 3, randomised, open-label study
-
McArthur GC, Chapman PB, Robert C, Larkin J, Haanen JB, Dummer R, et al. Safety and efficacy of vemurafanib in BRAF(V600E) and BRAF(V600K) mutation-positive melanoma (BRIM-3): extended follow-up of a phase 3, randomised, open-label study. Lancet Oncol 2014;15:323-32.
-
(2014)
Lancet Oncol
, vol.15
, pp. 323-332
-
-
McArthur, G.C.1
Chapman, P.B.2
Robert, C.3
Larkin, J.4
Haanen, J.B.5
Dummer, R.6
-
5
-
-
84864285704
-
Dabrafenib in BRAF-mutated metastatic melanoma: A multicentre, open-label, phase 3 randomised controlled trial
-
Hauschild A, Grob JJ, Demidov LV, Jouary T, Gutzmer R, Millward M, et al. Dabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial. Lancet 2012; 380: 358-65.
-
(2012)
Lancet
, vol.380
, pp. 358-365
-
-
Hauschild, A.1
Grob, J.J.2
Demidov, L.V.3
Jouary, T.4
Gutzmer, R.5
Millward, M.6
-
6
-
-
84903159476
-
Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyond
-
Holderfield M, Deuker MM, McCormick F, McMahon M. Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyond. Nat Rev Cancer 2014; 14: 455-67.
-
(2014)
Nat Rev Cancer
, vol.14
, pp. 455-467
-
-
Holderfield, M.1
Deuker, M.M.2
McCormick, F.3
McMahon, M.4
-
7
-
-
84887478023
-
Tumor adaptation and resistance to RAF inhibitors
-
Lito P, Rosen N, Solit DB. Tumor adaptation and resistance to RAF inhibitors. Nat Med 2013; 19: 1401-9.
-
(2013)
Nat Med
, vol.19
, pp. 1401-1409
-
-
Lito, P.1
Rosen, N.2
Solit, D.B.3
-
8
-
-
84892927755
-
Emerging insights into resistance to BRAF inhibitors in melanoma
-
Bucheit AD, Davies MA. Emerging insights into resistance to BRAF inhibitors in melanoma. Biochem Pharmacol 2014; 87: 381-9.
-
(2014)
Biochem Pharmacol
, vol.87
, pp. 381-389
-
-
Bucheit, A.D.1
Davies, M.A.2
-
9
-
-
84891898344
-
Acquired resistance and clonal evolution in melanoma during BRAF inhibitor therapy
-
Shi H, Hugo W, Kong X, Hong A, Koya RC, Moriceau G, et al. Acquired resistance and clonal evolution in melanoma during BRAF inhibitor therapy. Cancer Discov 2014; 4: 80-93.
-
(2014)
Cancer Discov
, vol.4
, pp. 80-93
-
-
Shi, H.1
Hugo, W.2
Kong, X.3
Hong, A.4
Koya, R.C.5
Moriceau, G.6
-
10
-
-
78650303507
-
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
-
Nazarian R, Shi H, Wang Q, Kong X, Koya RC, Lee H, et al. Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation. Nature 2010; 468: 973-7.
-
(2010)
Nature
, vol.468
, pp. 973-977
-
-
Nazarian, R.1
Shi, H.2
Wang, Q.3
Kong, X.4
Koya, R.C.5
Lee, H.6
-
11
-
-
84890062777
-
Differential AKT dependency displayed by mouse models of BRAFV600E-initiated melanoma
-
Marsh Durban V, Deuker MM, Bosenberg MW, Phillips W, McMahon M. Differential AKT dependency displayed by mouse models of BRAFV600E-initiated melanoma. J Clin Invest 2013; 123: 5104-18.
-
(2013)
J Clin Invest
, vol.123
, pp. 5104-5118
-
-
Marsh Durban, V.1
Deuker, M.M.2
Bosenberg, M.W.3
Phillips, W.4
McMahon, M.5
-
12
-
-
65649147543
-
Braf(V600E) cooperates with Pten loss to induce metastatic melanoma
-
Dankort D, Curley DP, Cartlidge RA, Nelson B, Karnezis AN, Damsky WE Jr, et al. Braf(V600E) cooperates with Pten loss to induce metastatic melanoma. Nat Genet 2009; 41: 544-52.
-
(2009)
Nat Genet
, vol.41
, pp. 544-552
-
-
Dankort, D.1
Curley, D.P.2
Cartlidge, R.A.3
Nelson, B.4
Karnezis, A.N.5
Damsky, W.E.6
-
13
-
-
1442274619
-
Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma
-
Tsao H, Goel V, Wu H, Yang G, Haluska FG. Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma. J Invest Dermatol 2004; 122: 337-41.
-
(2004)
J Invest Dermatol
, vol.122
, pp. 337-341
-
-
Tsao, H.1
Goel, V.2
Wu, H.3
Yang, G.4
Haluska, F.G.5
-
14
-
-
84865100965
-
Novel somatic mutations to PI3K pathway genes in metastatic melanoma
-
Shull AY, Latham-Schwark A, Ramasamy P, Leskoske K, Oroian D, Birtwistle MR, et al. Novel somatic mutations to PI3K pathway genes in metastatic melanoma. PLoS ONE 2012; 7: e43369.
-
(2012)
PLoS ONE
, vol.7
-
-
Shull, A.Y.1
Latham-Schwark, A.2
Ramasamy, P.3
Leskoske, K.4
Oroian, D.5
Birtwistle, M.R.6
-
15
-
-
84859204381
-
Comparison of growth factor signalling pathway utilisation in cultured normal melanocytes and melanoma cell lines
-
Kim JE, Stones C, Joseph WR, Leung E, Finlay GJ, Shelling AN, et al. Comparison of growth factor signalling pathway utilisation in cultured normal melanocytes and melanoma cell lines. BMC Cancer 2012; 12: 141.
-
(2012)
BMC Cancer
, vol.12
, pp. 141
-
-
Kim, J.E.1
Stones, C.2
Joseph, W.R.3
Leung, E.4
Finlay, G.J.5
Shelling, A.N.6
-
16
-
-
33845999615
-
Essential role for nuclear PTEN in maintaining chromosomal integrity
-
Shen WH, Balajee AS, Wang J, Wu H, Eng C, Pandolfi PP, et al. Essential role for nuclear PTEN in maintaining chromosomal integrity. Cell 2007; 128: 157-70.
-
(2007)
Cell
, vol.128
, pp. 157-170
-
-
Shen, W.H.1
Balajee, A.S.2
Wang, J.3
Wu, H.4
Eng, C.5
Pandolfi, P.P.6
-
17
-
-
78651482046
-
Nuclear PTEN regulates the APC-CDH1 tumor-suppressive complex in a phosphatase-independent manner
-
Song MS, Carracedo A, Salmena L, Song SJ, Egia A, Malumbres M, et al. Nuclear PTEN regulates the APC-CDH1 tumor-suppressive complex in a phosphatase-independent manner. Cell 2011; 144: 187- 99.
-
(2011)
Cell
, vol.144
, pp. 187-199
-
-
Song, M.S.1
Carracedo, A.2
Salmena, L.3
Song, S.J.4
Egia, A.5
Malumbres, M.6
-
18
-
-
0038456399
-
PTEN signaling pathways in melanoma
-
Wu H, Goel V, Haluska FG. PTEN signaling pathways in melanoma. Oncogene 2003; 22: 3113-22.
-
(2003)
Oncogene
, vol.22
, pp. 3113-3122
-
-
Wu, H.1
Goel, V.2
Haluska, F.G.3
-
19
-
-
84878836487
-
Discovery of NVP-BYL719 a potent and selective phosphatidylinositol- 3 kinase alpha inhibitor selected for clinical evaluation
-
Furet P, Guagnano V, Fairhurst RA, Imbach-Weese P, Bruce I, Knapp M, et al. Discovery of NVP-BYL719 a potent and selective phosphatidylinositol- 3 kinase alpha inhibitor selected for clinical evaluation. Bioorg Med Chem Lett 2013; 23: 3741-8.
-
(2013)
Bioorg Med Chem Lett
, vol.23
, pp. 3741-3748
-
-
Furet, P.1
Guagnano, V.2
Fairhurst, R.A.3
Imbach-Weese, P.4
Bruce, I.5
Knapp, M.6
-
20
-
-
84897067467
-
BRAFV600E cooperates with PI3K signaling, independent of AKT, to regulate melanoma cell proliferation
-
Silva JM, Bulman C, McMahon M. BRAFV600E cooperates with PI3K signaling, independent of AKT, to regulate melanoma cell proliferation. Mol Cancer Res 2014; 12: 447-63.
-
(2014)
Mol Cancer Res
, vol.12
, pp. 447-463
-
-
Silva, J.M.1
Bulman, C.2
McMahon, M.3
-
21
-
-
84868033582
-
Preclinical profile of LGX818: A potent and selective RAF kinase inhibitor
-
Stuart DD, Li N, Poon DJ, Aardalen K, Kaufman S, Merritt H, et al. Preclinical profile of LGX818: A potent and selective RAF kinase inhibitor. AACR 103rd Annual Meeting, Cancer Res 2012;72:3790.
-
(2012)
AACR 103rd Annual Meeting, Cancer Res
, vol.72
, pp. 3790
-
-
Stuart, D.D.1
Li, N.2
Poon, D.J.3
Aardalen, K.4
Kaufman, S.5
Merritt, H.6
-
22
-
-
84861163796
-
Abrogation of BRAFV600E-induced senescence by PI3K pathway activation contributes to melanomagenesis
-
Vredeveld LC, Possik PA, Smit MA, Meissl K, Michaloglou C, Horlings HM, et al. Abrogation of BRAFV600E-induced senescence by PI3K pathway activation contributes to melanomagenesis. Genes Dev 2012; 26: 1055-69.
-
(2012)
Genes Dev
, vol.26
, pp. 1055-1069
-
-
Vredeveld, L.C.1
Possik, P.A.2
Smit, M.A.3
Meissl, K.4
Michaloglou, C.5
Horlings, H.M.6
-
23
-
-
57849117384
-
New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
-
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 2009; 45: 228-47.
-
(2009)
Eur J Cancer
, vol.45
, pp. 228-247
-
-
Eisenhauer, E.A.1
Therasse, P.2
Bogaerts, J.3
Schwartz, L.H.4
Sargent, D.5
Ford, R.6
-
24
-
-
51349148948
-
PTEN-deficient cancers depend on PIK3CB
-
Wee S, Wiederschain D, Maira SM, Loo A, Miller C, deBeaumont R, et al. PTEN-deficient cancers depend on PIK3CB. Proc Natl Acad Sci U S A 2008; 105: 13057-62.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 13057-13062
-
-
Wee, S.1
Wiederschain, D.2
Maira, S.M.3
Loo, A.4
Miller, C.5
deBeaumont, R.6
-
25
-
-
49649087385
-
Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis
-
Jia S, Liu Z, Zhang S, Liu P, Zhang L, Lee SH, et al. Essential roles of PI(3)K-p110beta in cell growth, metabolism and tumorigenesis. Nature 2008; 454: 776-9.
-
(2008)
Nature
, vol.454
, pp. 776-779
-
-
Jia, S.1
Liu, Z.2
Zhang, S.3
Liu, P.4
Zhang, L.5
Lee, S.H.6
-
26
-
-
21044454703
-
PI 3-kinase p110beta: A new target for antithrombotic therapy
-
Jackson SP, Schoenwaelder SM, Goncalves I, Nesbitt WS, Yap CL, Wright CE, et al. PI 3-kinase p110beta: a new target for antithrombotic therapy. Nat Med 2005; 11: 507-14.
-
(2005)
Nat Med
, vol.11
, pp. 507-514
-
-
Jackson, S.P.1
Schoenwaelder, S.M.2
Goncalves, I.3
Nesbitt, W.S.4
Yap, C.L.5
Wright, C.E.6
-
27
-
-
84875143933
-
Identification of GSK2636771, a potent and selective, orally bioavailable inhibitor of phosphatidylinositol 3-kinase-beta for the treatment of PTEN deficient tumors
-
Rivero RA, Hardwicke M. Identification of GSK2636771, a potent and selective, orally bioavailable inhibitor of phosphatidylinositol 3-kinase-beta for the treatment of PTEN deficient tumors. AACR 103rd Annual Meeting, Cancer Res 2012;72:2913.
-
(2012)
AACR 103rd Annual Meeting, Cancer Res
, vol.72
, pp. 2913
-
-
Rivero, R.A.1
Hardwicke, M.2
-
28
-
-
84863833204
-
Functional characterization of an isoform-selective inhibitor of PI3K-p110beta as a potential anticancer agent
-
Ni J, Liu Q, Xie S, Carlson C, Von T, Vogel K, et al. Functional characterization of an isoform-selective inhibitor of PI3K-p110beta as a potential anticancer agent. Cancer Discov 2012; 2: 425-33.
-
(2012)
Cancer Discov
, vol.2
, pp. 425-433
-
-
Ni, J.1
Liu, Q.2
Xie, S.3
Carlson, C.4
Von, T.5
Vogel, K.6
-
29
-
-
84879056371
-
Discovery of 2-{3-[2-(1-isopropyl-3-methyl-1H-1,2- 4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl]- 1H-pyrazol-1-yl}-2-methylpropanamide (GDC-0032): A beta-sparing phosphoinositide 3-kinase inhibitor with high unbound exposure and robust in vivo antitumor activity
-
Ndubaku CO, Heffron TP, Staben ST, Baumgardner M, Blaquiere N, Bradley E, et al. Discovery of 2-{3-[2-(1-isopropyl-3-methyl-1H-1,2- 4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl]- 1H-pyrazol-1-yl}-2-methylpropanamide (GDC-0032): a beta-sparing phosphoinositide 3-kinase inhibitor with high unbound exposure and robust in vivo antitumor activity. J Med Chem 2013; 56: 4597- 610.
-
(2013)
J Med Chem
, vol.56
, pp. 4597-4610
-
-
Ndubaku, C.O.1
Heffron, T.P.2
Staben, S.T.3
Baumgardner, M.4
Blaquiere, N.5
Bradley, E.6
-
30
-
-
52449106253
-
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin- 1-ylmethyl)-4-morpholin-4-yl-t hieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
-
Folkes AJ, Ahmadi K, Alderton WK, Alix S, Baker SJ, Box G, et al. The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin- 1-ylmethyl)-4-morpholin-4-yl-t hieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer. J Med Chem 2008; 51: 5522-32.
-
(2008)
J Med Chem
, vol.51
, pp. 5522-5532
-
-
Folkes, A.J.1
Ahmadi, K.2
Alderton, W.K.3
Alix, S.4
Baker, S.J.5
Box, G.6
-
31
-
-
84888219144
-
PI3K-delta and PI3K-gamma inhibition by IPI-145 abrogates immune responses and suppresses activity in autoimmune and inflammatory disease models
-
Winkler DG, Faia KL, DiNitto JP, Ali JA, White KF, Brophy EE, et al. PI3K-delta and PI3K-gamma inhibition by IPI-145 abrogates immune responses and suppresses activity in autoimmune and inflammatory disease models. Chem Biol 2013; 20: 1364-74.
-
(2013)
Chem Biol
, vol.20
, pp. 1364-1374
-
-
Winkler, D.G.1
Faia, K.L.2
DiNitto, J.P.3
Ali, J.A.4
White, K.F.5
Brophy, E.E.6
-
32
-
-
84861017745
-
Novel carboxamide-based allosteric MEK inhibitors: Discovery and optimization efforts toward XL518 (GDC-0973)
-
Rice KD, Aay N, Anand NK, Blazey CM, Bowles OJ, Bussenius J, et al. Novel carboxamide-based allosteric MEK inhibitors: discovery and optimization efforts toward XL518 (GDC-0973). ACS Med Chem Lett 2012; 3: 416-21.
-
(2012)
ACS Med Chem Lett
, vol.3
, pp. 416-421
-
-
Rice, K.D.1
Aay, N.2
Anand, N.K.3
Blazey, C.M.4
Bowles, O.J.5
Bussenius, J.6
-
33
-
-
0037025173
-
Cancer. Addiction to oncogenes-the Achilles heal of cancer
-
Weinstein IB. Cancer. Addiction to oncogenes-the Achilles heal of cancer. Science 2002; 297: 63-4.
-
(2002)
Science
, vol.297
, pp. 63-64
-
-
Weinstein, I.B.1
-
34
-
-
44849093562
-
Oncogene addiction
-
discussion 80
-
Weinstein IB, Joe A. Oncogene addiction. Cancer Res 2008; 68: 3077-80; discussion 80.
-
(2008)
Cancer Res
, vol.68
, pp. 3077-3080
-
-
Weinstein, I.B.1
Joe, A.2
-
35
-
-
84878288766
-
RAS and RHO families of GTPases directly regulate distinct phosphoinositide 3-kinase isoforms
-
Fritsch R, de Krijger I, Fritsch K, George R, Reason B, Kumar MS, et al. RAS and RHO families of GTPases directly regulate distinct phosphoinositide 3-kinase isoforms. Cell 2013; 153: 1050-63.
-
(2013)
Cell
, vol.153
, pp. 1050-1063
-
-
Fritsch, R.1
de Krijger, I.2
Fritsch, K.3
George, R.4
Reason, B.5
Kumar, M.S.6
-
36
-
-
84904555503
-
Phase I dose-escalation and -expansion study of buparlisib (BKM120), an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors
-
Rodon J, Brana I, Siu LL, De Jonge MJ, Homji N, Mills D, et al. Phase I dose-escalation and -expansion study of buparlisib (BKM120), an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors. Invest New Drugs 2014; 32: 670-81.
-
(2014)
Invest New Drugs
, vol.32
, pp. 670-681
-
-
Rodon, J.1
Brana, I.2
Siu, L.L.3
De Jonge, M.J.4
Homji, N.5
Mills, D.6
-
37
-
-
77950954465
-
Differential sensitivity of melanoma cell lines with BRAFV600E mutation to the specific Raf inhibitor PLX4032
-
Sondergaard JN, Nazarian R, Wang Q, Guo D, Hsueh T, Mok S, et al. Differential sensitivity of melanoma cell lines with BRAFV600E mutation to the specific Raf inhibitor PLX4032. J Translational Med 2010; 8: 39.
-
(2010)
J Translational Med
, vol.8
, pp. 39
-
-
Sondergaard, J.N.1
Nazarian, R.2
Wang, Q.3
Guo, D.4
Hsueh, T.5
Mok, S.6
-
38
-
-
83455254767
-
RAF inhibitor resistance is mediated by dimerization of aberrantly spliced BRAF(V600E)
-
Poulikakos PI, Persaud Y, Janakiraman M, Kong X, Ng C, Moriceau G, et al. RAF inhibitor resistance is mediated by dimerization of aberrantly spliced BRAF(V600E). Nature 2011; 480: 387-90.
-
(2011)
Nature
, vol.480
, pp. 387-390
-
-
Poulikakos, P.I.1
Persaud, Y.2
Janakiraman, M.3
Kong, X.4
Ng, C.5
Moriceau, G.6
-
39
-
-
0033014481
-
Body condition scoring: A rapid and accurate method for assessing health status in mice
-
Ullman-Cullere MH, Foltz CJ. Body condition scoring: a rapid and accurate method for assessing health status in mice. Lab Anim Sci 1999; 49: 319-23.
-
(1999)
Lab Anim Sci
, vol.49
, pp. 319-323
-
-
Ullman-Cullere, M.H.1
Foltz, C.J.2
|