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Volumn 11, Issue 5, 2012, Pages 1143-1154

ERK inhibition overcomes acquired resistance to MEK Inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME INHIBITOR; G 573; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; N (2,3 DIHYDROXYPROPOXY) 3,4 DIFLUORO 2 (2 FLUORO 4 IODOANILINO)BENZAMIDE; UNCLASSIFIED DRUG;

EID: 84862726767     PISSN: 15357163     EISSN: 15388514     Source Type: Journal    
DOI: 10.1158/1535-7163.MCT-11-1010     Document Type: Article
Times cited : (181)

References (41)
  • 1
    • 34248591612 scopus 로고    scopus 로고
    • Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
    • DOI 10.1038/sj.onc.1210422, PII 1210422
    • Roberts PJ, Der CJ. Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer. Oncogene 2007;26:3291-310. (Pubitemid 46763022)
    • (2007) Oncogene , vol.26 , Issue.22 , pp. 3291-3310
    • Roberts, P.J.1    Der, C.J.2
  • 3
    • 79951961755 scopus 로고    scopus 로고
    • Resistance to BRA Finhibition in melanomas
    • Solit DB, Rosen N. Resistance to BRA Finhibition in melanomas. N Engl J Med 2011;364:772-4.
    • (2011) N Engl J Med , vol.364 , pp. 772-774
    • Solit, D.B.1    Rosen, N.2
  • 4
    • 78650008177 scopus 로고    scopus 로고
    • Acquired resistance to BRAF inhibitors mediated by a RAF kinase switch in melanoma can be overcome by cotargeting MEK and IGF-1R/PI3K
    • Villanueva J, Vultur A, Lee JT, Somasundaram R, Fukunaga-Kalabis M, Cipolla AK, et al. Acquired resistance to BRAF inhibitors mediated by a RAF kinase switch in melanoma can be overcome by cotargeting MEK and IGF-1R/PI3K. Cancer Cell 2010;18:683-95.
    • (2010) Cancer Cell , vol.18 , pp. 683-695
    • Villanueva, J.1    Vultur, A.2    Lee, J.T.3    Somasundaram, R.4    Fukunaga-Kalabis, M.5    Cipolla, A.K.6
  • 5
    • 78650303507 scopus 로고    scopus 로고
    • 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
  • 7
    • 80051625929 scopus 로고    scopus 로고
    • Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling
    • Wagle N, Emery C, Berger MF, Davis MJ, Sawyer A, Pochanard P, et al. Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling. J Clin Oncol 2011;29:3085-96.
    • (2011) J Clin Oncol , vol.29 , pp. 3085-3096
    • Wagle, N.1    Emery, C.2    Berger, M.F.3    Davis, M.J.4    Sawyer, A.5    Pochanard, P.6
  • 8
    • 78649436372 scopus 로고    scopus 로고
    • BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation
    • Corcoran RB, Dias-Santagata D, Bergethon K, Iafrate AJ, Settleman J, Engelman JA. BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation. Sci Signal 2011;3:ra84.
    • (2011) Sci Signal , vol.3
    • Corcoran, R.B.1    Dias-Santagata, D.2    Bergethon, K.3    Iafrate, A.J.4    Settleman, J.5    Engelman, J.A.6
  • 9
    • 79956105175 scopus 로고    scopus 로고
    • STAT3 mediates resistance to MEK inhibitor through microRNA miR-17
    • Dai B, Meng J, Peyton M, Girard L, Bornmann WG, Ji L, et al. STAT3 mediates resistance to MEK inhibitor through microRNA miR-17. Cancer Res 2011;71:3658-68.
    • (2011) Cancer Res , vol.71 , pp. 3658-3668
    • Dai, B.1    Meng, J.2    Peyton, M.3    Girard, L.4    Bornmann, W.G.5    Ji, L.6
  • 10
    • 80051687428 scopus 로고    scopus 로고
    • Identification of the MEK1(F129L) activating mutation as a potential mechanism of acquired resistance to MEK inhibition in human cancers carrying the B-RafV600E mutation
    • Wang H, Daouti S, Li WH, Wen Y, Rizzo C, Higgins B, et al. Identification of the MEK1(F129L) activating mutation as a potential mechanism of acquired resistance to MEK inhibition in human cancers carrying the B-RafV600E mutation. Cancer Res 2011;71:5535-45.
    • (2011) Cancer Res , vol.71 , pp. 5535-5545
    • Wang, H.1    Daouti, S.2    Li, W.H.3    Wen, Y.4    Rizzo, C.5    Higgins, B.6
  • 12
    • 70350066163 scopus 로고    scopus 로고
    • Structure-guided design of potent and selective pyrimidylpyrrole inhibitors of extracellular signal-regulated kinase (ERK) using conformational control
    • Aronov AM, Tang Q, Martinez-Botella G, Bemis GW, Cao J, Chen G, et al. Structure-guided design of potent and selective pyrimidylpyrrole inhibitors of extracellular signal-regulated kinase (ERK) using conformational control. J Med Chem 2009;52:6362-8.
    • (2009) J Med Chem , vol.52 , pp. 6362-6368
    • Aronov, A.M.1    Tang, Q.2    Martinez-Botella, G.3    Bemis, G.W.4    Cao, J.5    Chen, G.6
  • 13
    • 84862731266 scopus 로고    scopus 로고
    • Pyrrole inhibitors of ERK protein kinase, synthesis thereof and intermediates thereto
    • patent US patent number 7,354,939 B2
    • Martinez-Botella G, Hale M, Maltais F, Straub J, Tang Q inventor "Pyrrole inhibitors of ERK protein kinase, synthesis thereof and intermediates thereto" patent US patent number 7,354,939 B2. 2008.
    • (2008)
    • Martinez-Botella, G.1    Hale, M.2    Maltais, F.3    Straub, J.4    Tang, Q.5
  • 14
    • 33847095086 scopus 로고    scopus 로고
    • Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration
    • DOI 10.1007/s00280-006-0323-5
    • Brown AP, Carlson TC, Loi CM, Graziano MJ. Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration. Cancer Chemother Pharmacol 2007;59:671-9. (Pubitemid 46295133)
    • (2007) Cancer Chemotherapy and Pharmacology , vol.59 , Issue.5 , pp. 671-679
    • Brown, A.P.1    Carlson, T.C.G.2    Loi, C.-M.3    Graziano, M.J.4
  • 15
    • 77957954252 scopus 로고    scopus 로고
    • Preclinical disposition and pharmacokinetics-pharmacodynamic modeling of biomarker response and tumour growth inhibition in xenograft mouse models of G-573, a MEK inhibitor
    • Choo EF, Belvin M, Chan J, Hoeflich K, Orr C, Robarge K, et al. Preclinical disposition and pharmacokinetics-pharmacodynamic modeling of biomarker response and tumour growth inhibition in xenograft mouse models of G-573, a MEK inhibitor. Xenobiotica 2010;40:751-62.
    • (2010) Xenobiotica , vol.40 , pp. 751-762
    • Choo, E.F.1    Belvin, M.2    Chan, J.3    Hoeflich, K.4    Orr, C.5    Robarge, K.6
  • 16
    • 52449106253 scopus 로고    scopus 로고
    • The identification of 2-(1H-Indazol-4-yl)-6-(4-methanesulfonyl-piperazin- 1-ylmethyl)-4-morpholin-4-yl-thieno[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-thieno[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
  • 17
    • 77952936250 scopus 로고    scopus 로고
    • PLX-4032, a small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma
    • Smalley KS. PLX-4032, a small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma. Curr Opin Investig Drugs 2010;11:699-706.
    • (2010) Curr Opin Investig Drugs , vol.11 , pp. 699-706
    • Smalley, K.S.1
  • 18
    • 77249137785 scopus 로고    scopus 로고
    • Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer
    • Sutherlin DP, Sampath D, Berry M, Castanedo G, Chang Z, Chuckowree I, et al. Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer. J Med Chem 2011;53:1086-97.
    • (2011) J Med Chem , vol.53 , pp. 1086-1097
    • Sutherlin, D.P.1    Sampath, D.2    Berry, M.3    Castanedo, G.4    Chang, Z.5    Chuckowree, I.6
  • 19
    • 77954755623 scopus 로고    scopus 로고
    • Predictive biomarkers of sensitivity to the phosphatidylinositol 3′ kinase inhibitor GDC-0941 in breast cancer preclinical models
    • O'Brien C, Wallin JJ, Sampath D, GuhaThakurta D, Savage H, Punnoose EA, et al. Predictive biomarkers of sensitivity to the phosphatidylinositol 3′ kinase inhibitor GDC-0941 in breast cancer preclinical models. Clin Cancer Res 2010;16:3670-83.
    • (2010) Clin Cancer Res , vol.16 , pp. 3670-3683
    • O'Brien, C.1    Wallin, J.J.2    Sampath, D.3    GuhaThakurta, D.4    Savage, H.5    Punnoose, E.A.6
  • 20
    • 68049085887 scopus 로고    scopus 로고
    • In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models
    • Hoeflich KP, O'Brien C, Boyd Z, Cavet G, Guerrero S, Jung K, et al. In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models. Clin Cancer Res 2009;15:4649-64.
    • (2009) Clin Cancer Res , vol.15 , pp. 4649-4664
    • Hoeflich, K.P.1    O'Brien, C.2    Boyd, Z.3    Cavet, G.4    Guerrero, S.5    Jung, K.6
  • 23
    • 56049110212 scopus 로고    scopus 로고
    • Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms
    • Diskin SJ, Li M, Hou C, Yang S, Glessner J, Hakonarson H, et al. Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. Nucleic Acids Res 2008;36:e126.
    • (2008) Nucleic Acids Res , vol.36
    • Diskin, S.J.1    Li, M.2    Hou, C.3    Yang, S.4    Glessner, J.5    Hakonarson, H.6
  • 24
    • 34147104969 scopus 로고    scopus 로고
    • A faster circular binary segmentation algorithm for the analysis of array CGH data
    • DOI 10.1093/bioinformatics/btl646
    • Venkatraman ES, Olshen AB. A faster circular binary segmentation algorithm for the analysis of array CGH data. Bioinformatics 2007;23:657-63. (Pubitemid 46554715)
    • (2007) Bioinformatics , vol.23 , Issue.6 , pp. 657-663
    • Venkatraman, E.S.1    Olshen, A.B.2
  • 25
    • 56049103793 scopus 로고    scopus 로고
    • Understanding and treating triple-negative breast cancer
    • Williston Park discussion 9-40, 43
    • Anders C, Carey LA. Understanding and treating triple-negative breast cancer. Oncology (Williston Park) 2008;22:1233-9; discussion 9-40, 43.
    • (2008) Oncology , vol.22 , pp. 1233-1239
    • Anders, C.1    Carey, L.A.2
  • 27
    • 58349091262 scopus 로고    scopus 로고
    • Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition
    • Mirzoeva OK, Das D, Heiser LM, Bhattacharya S, Siwak D, Gendelman R, et al. Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition. Cancer Res 2009;69:565-72.
    • (2009) Cancer Res , vol.69 , pp. 565-572
    • Mirzoeva, O.K.1    Das, D.2    Heiser, L.M.3    Bhattacharya, S.4    Siwak, D.5    Gendelman, R.6
  • 28
    • 34548822459 scopus 로고    scopus 로고
    • Recent advances of MEK inhibitors and their clinical progress
    • DOI 10.2174/156802607781696837
    • Wang JY, Wilcoxen KM, Nomoto K, Wu S. Recent advances of MEK inhibitors and their clinical progress. Curr Top Med Chem 2007;7:1364-78. (Pubitemid 47471235)
    • (2007) Current Topics in Medicinal Chemistry , vol.7 , Issue.14 , pp. 1364-1378
    • Wang, J.1    Wilcoxen, K.M.2    Nomoto, K.3    Wu, S.4
  • 31
    • 79959216175 scopus 로고    scopus 로고
    • TRPS1 targeting by miR-221/222 promotes the epithelial-to-mesenchymal transition in breast cancer
    • Stinson S, Lackner MR, Adai AT, Yu N, Kim HJ, O'Brien C, et al. TRPS1 targeting by miR-221/222 promotes the epithelial-to-mesenchymal transition in breast cancer. Sci Signal 2011;4:ra41.
    • (2011) Sci Signal , vol.4
    • Stinson, S.1    Lackner, M.R.2    Adai, A.T.3    Yu, N.4    Kim, H.J.5    O'Brien, C.6
  • 33
    • 79953240219 scopus 로고    scopus 로고
    • Amplification of the driving oncogene, KRAS or BRAF, underpins acquired resistance to MEK1/2 inhibitors in colorectal cancer cells
    • Little AS, Balmanno K, Sale MJ, Newman S, Dry JR, Hampson M, et al. Amplification of the driving oncogene, KRAS or BRAF, underpins acquired resistance to MEK1/2 inhibitors in colorectal cancer cells. Sci Signal 2011;4:ra17.
    • (2011) Sci Signal , vol.4
    • Little, A.S.1    Balmanno, K.2    Sale, M.J.3    Newman, S.4    Dry, J.R.5    Hampson, M.6
  • 34
    • 79951818749 scopus 로고    scopus 로고
    • MEK-independent survival of B-RAFV600E melanoma cells selected for resistance to apoptosis induced by the RAF inhibitor PLX4720
    • Jiang CC, Lai F, Thorne RF, Yang F, Liu H, Hersey P, et al. MEK-independent survival of B-RAFV600E melanoma cells selected for resistance to apoptosis induced by the RAF inhibitor PLX4720. Clin Cancer Res 2011;17:721-30.
    • (2011) Clin Cancer Res , vol.17 , pp. 721-730
    • Jiang, C.C.1    Lai, F.2    Thorne, R.F.3    Yang, F.4    Liu, H.5    Hersey, P.6
  • 35
    • 84946384873 scopus 로고
    • The toxicity of poisons applied jointly
    • CI B. The toxicity of poisons applied jointly. Ann Appl Biol 1939;26:585-615.
    • (1939) Ann Appl Biol , vol.26 , pp. 585-615
    • Ci, B.1
  • 36
    • 0030570139 scopus 로고    scopus 로고
    • The search for cytotoxic synergy between anticancer agents: A case of Dorothy and the ruby slippers?
    • Greco WR, Faessel H, Levasseur L. The search for cytotoxic synergy between anticancer agents: a case of Dorothy and the ruby slippers? J Natl Cancer Inst 1996;88:699-700.
    • (1996) J Natl Cancer Inst , vol.88 , pp. 699-700
    • Greco, W.R.1    Faessel, H.2    Levasseur, L.3
  • 39
    • 80555157475 scopus 로고    scopus 로고
    • Receptor tyrosine kinases exert dominant control over PI3K signaling in human KRAS mutant colorectal cancers
    • Ebi H, Corcoran RB, Singh A, Chen Z, Song Y, Lifshits E, et al. Receptor tyrosine kinases exert dominant control over PI3K signaling in human KRAS mutant colorectal cancers. J Clin Invest 2011;121:4311-21.
    • (2011) J Clin Invest , vol.121 , pp. 4311-4321
    • Ebi, H.1    Corcoran, R.B.2    Singh, A.3    Chen, Z.4    Song, Y.5    Lifshits, E.6
  • 41
    • 80053154225 scopus 로고    scopus 로고
    • Phase I/II study to assess safety, pharmacokinetics, and efficacy of the oral MEK 1/2 inhibitor GSK1120212 (GSK212) dosed in combination with the oral BRAF inhibitor GSK2118436 (GSK436)
    • Infante JR, Falchook GS, Lawrence DP, Weber JS, Kefford RF, Bendell JC, et al. Phase I/II study to assess safety, pharmacokinetics, and efficacy of the oral MEK 1/2 inhibitor GSK1120212 (GSK212) dosed in combination with the oral BRAF inhibitor GSK2118436 (GSK436). J Clin Oncol (supplement) 2011;29.
    • (2011) J Clin Oncol , Issue.SUPPL. , pp. 29
    • Infante, J.R.1    Falchook, G.S.2    Lawrence, D.P.3    Weber, J.S.4    Kefford, R.F.5    Bendell, J.C.6


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