메뉴 건너뛰기




Volumn 91, Issue 4, 2014, Pages 417-425

Change or die: Targeting adaptive signaling to kinase inhibition in cancer cells

Author keywords

BRAF; Melanoma; NRAS; Phosphoproteomics; Signaling

Indexed keywords

ADAPTOR PROTEIN; GUANINE NUCLEOTIDE EXCHANGE FACTOR; GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN; MAMMALIAN TARGET OF RAPAMYCIN; PROTEIN KINASE B; PROTEIN SH3; PROTEIN TYROSINE KINASE; PROTEIN KINASE; PROTEIN KINASE INHIBITOR;

EID: 84921628212     PISSN: 00062952     EISSN: 18732968     Source Type: Journal    
DOI: 10.1016/j.bcp.2014.07.031     Document Type: Note
Times cited : (9)

References (100)
  • 1
    • 67749086812 scopus 로고    scopus 로고
    • The PTEN-AKT3 signaling cascade as a therapeutic target in melanoma
    • Madhunapantula SV, Robertson GP. The PTEN-AKT3 signaling cascade as a therapeutic target in melanoma. Pigment Cell Melanoma Res 2009;22:400-19.
    • (2009) Pigment Cell Melanoma Res , vol.22 , pp. 400-419
    • Madhunapantula, S.V.1    Robertson, G.P.2
  • 2
    • 84877590959 scopus 로고    scopus 로고
    • MAP kinase signaling and inhibition in melanoma
    • Sullivan RJ, Flaherty K. MAP kinase signaling and inhibition in melanoma. Oncogene 2013;32:2373-9.
    • (2013) Oncogene , vol.32 , pp. 2373-2379
    • Sullivan, R.J.1    Flaherty, K.2
  • 3
    • 84864285704 scopus 로고    scopus 로고
    • Dabrafenib in BRAF-mutated metastatic melanoma: A multicentre, openlabel, 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, openlabel, 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
    • 77954615408 scopus 로고    scopus 로고
    • MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
    • Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, Tsujioka K, et al. 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;9:1956-67.
    • (2010) Mol Cancer Ther , vol.9 , pp. 1956-1967
    • Hirai, H.1    Sootome, H.2    Nakatsuru, Y.3    Miyama, K.4    Taguchi, S.5    Tsujioka, K.6
  • 9
    • 77954212739 scopus 로고    scopus 로고
    • Targeting epidermal growth factor receptor: Central signaling kinase in lung cancer
    • Yoshida T, Zhang G, Haura EB. Targeting epidermal growth factor receptor: central signaling kinase in lung cancer. Biochem Pharmacol 2010;80: 613-23.
    • (2010) Biochem Pharmacol , vol.80 , pp. 613-623
    • Yoshida, T.1    Zhang, G.2    Haura, E.B.3
  • 11
    • 79956318797 scopus 로고    scopus 로고
    • Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK
    • Katayama R, Khan TM, Benes C, Lifshits E, Ebi H, Rivera VM, et al. Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK. Proc Natl Acad Sci USA 2011;108: 7535-40.
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 7535-7540
    • Katayama, R.1    Khan, T.M.2    Benes, C.3    Lifshits, E.4    Ebi, H.5    Rivera, V.M.6
  • 12
    • 77954213847 scopus 로고    scopus 로고
    • Targeted therapies of gastrointestinal stromal tumors (GIST) -The next frontiers
    • Duensing S, Duensing A. Targeted therapies of gastrointestinal stromal tumors (GIST)-the next frontiers. Biochem Pharmacol 2010;80:575-83.
    • (2010) Biochem Pharmacol , vol.80 , pp. 575-583
    • Duensing, S.1    Duensing, A.2
  • 13
    • 46449103344 scopus 로고    scopus 로고
    • TAM receptor tyrosine kinases: Biologic functions, signaling, and potential therapeutic targeting in human cancer
    • Linger RM, Keating AK, Earp HS, Graham DK. TAM receptor tyrosine kinases: biologic functions, signaling, and potential therapeutic targeting in human cancer. Adv Cancer Res 2008;100:35-83.
    • (2008) Adv Cancer Res , vol.100 , pp. 35-83
    • Linger, R.M.1    Keating, A.K.2    Earp, H.S.3    Graham, D.K.4
  • 14
    • 0034789517 scopus 로고    scopus 로고
    • Receptor tyrosine kinase signalling as a target for cancer intervention strategies
    • Zwick E, Bange J, Ullrich A. Receptor tyrosine kinase signalling as a target for cancer intervention strategies. Endocr Relat Cancer 2001;8:161-73.
    • (2001) Endocr Relat Cancer , vol.8 , pp. 161-173
    • Zwick, E.1    Bange, J.2    Ullrich, A.3
  • 15
    • 0035107205 scopus 로고    scopus 로고
    • The discoidin domain receptor tyrosine kinase DDR1 in arterial wound repair
    • Hou G, Vogel W, Bendeck MP. The discoidin domain receptor tyrosine kinase DDR1 in arterial wound repair. J Clin Invest 2001;107:727-35.
    • (2001) J Clin Invest , vol.107 , pp. 727-735
    • Hou, G.1    Vogel, W.2    Bendeck, M.P.3
  • 17
    • 79960066478 scopus 로고    scopus 로고
    • Mammalian son of sevenless Guanine nucleotide exchange factors: Old concepts and new perspectives
    • Rojas JM, Oliva JL, Santos E. Mammalian son of sevenless Guanine nucleotide exchange factors: old concepts and new perspectives. Genes Cancer 2011;2: 298-305.
    • (2011) Genes Cancer , vol.2 , pp. 298-305
    • Rojas, J.M.1    Oliva, J.L.2    Santos, E.3
  • 18
    • 45449092590 scopus 로고    scopus 로고
    • SnapShot: Ras signaling
    • Cully M, Downward J. SnapShot: Ras signaling. Cell 2008;133:1292-301.
    • (2008) Cell , vol.133 , pp. 1292-1301
    • Cully, M.1    Downward, J.2
  • 19
    • 0037264633 scopus 로고    scopus 로고
    • Targeting RAS signalling pathways in cancer therapy
    • Downward J. Targeting RAS signalling pathways in cancer therapy. Nat Rev Cancer 2003;3:11-22.
    • (2003) Nat Rev Cancer , vol.3 , pp. 11-22
    • Downward, J.1
  • 20
    • 0037805547 scopus 로고    scopus 로고
    • RAS oncogenes: The first 30 years
    • Malumbres M, Barbacid M. RAS oncogenes: the first 30 years. Nat Rev Cancer 2003;3:459-65.
    • (2003) Nat Rev Cancer , vol.3 , pp. 459-465
    • Malumbres, M.1    Barbacid, M.2
  • 22
    • 2942568167 scopus 로고    scopus 로고
    • Modulation of signalling by Sprouty: A developing story
    • Kim HJ, Bar-Sagi D. Modulation of signalling by Sprouty: a developing story. Nat Rev Mol Cell Biol 2004;5:441-50.
    • (2004) Nat Rev Mol Cell Biol , vol.5 , pp. 441-450
    • Kim, H.J.1    Bar-Sagi, D.2
  • 23
    • 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
  • 25
    • 78650309875 scopus 로고    scopus 로고
    • COT drives resistance to RAF inhibition through MAP kinase pathway reacti-vation
    • Johannessen CM, Boehm JS, Kim SY, Thomas SR, Wardwell L, Johnson LA, et al. COT drives resistance to RAF inhibition through MAP kinase pathway reacti-vation. Nature 2010;468(7326):968-72.
    • (2010) Nature , vol.468 , Issue.7326 , pp. 968-972
    • Johannessen, C.M.1    Boehm, J.S.2    Kim, S.Y.3    Thomas, S.R.4    Wardwell, L.5    Johnson, L.A.6
  • 26
    • 84877293970 scopus 로고    scopus 로고
    • P21-activated kinase 1 (PAK1) is a therapeutic target in BRAF wild-type melano-ma
    • Ong CC, Jubb AM, Jakubiak D, Zhou W, Rudolph J, Haverty PM, et al. P21-activated kinase 1 (PAK1) is a therapeutic target in BRAF wild-type melano-ma. J Natl Cancer Inst 2013;105(9):606-7.
    • (2013) J Natl Cancer Inst , vol.105 , Issue.9 , pp. 606-607
    • Ong, C.C.1    Jubb, A.M.2    Jakubiak, D.3    Zhou, W.4    Rudolph, J.5    Haverty, P.M.6
  • 27
    • 19644397029 scopus 로고    scopus 로고
    • Adhesion control of cyclin D1 and p27Kip1 levels is deregulated in melanoma cells through BRAF-MEK-ERK signaling
    • Bhatt KV, Spofford LS, Aram G, McMullen M, Pumiglia K, Aplin AE. Adhesion control of cyclin D1 and p27Kip1 levels is deregulated in melanoma cells through BRAF-MEK-ERK signaling. Oncogene 2005;24:3459-71.
    • (2005) Oncogene , vol.24 , pp. 3459-3471
    • Bhatt, K.V.1    Spofford, L.S.2    Aram, G.3    McMullen, M.4    Pumiglia, K.5    Aplin, A.E.6
  • 29
    • 65549130220 scopus 로고    scopus 로고
    • Rnd3 regulation of the actin cytoskeleton promotes melanoma migration and invasive outgrowth in three dimensions
    • Klein RM, Aplin AE. Rnd3 regulation of the actin cytoskeleton promotes melanoma migration and invasive outgrowth in three dimensions. Cancer Res 2009;69:2224-33.
    • (2009) Cancer Res , vol.69 , pp. 2224-2233
    • Klein, R.M.1    Aplin, A.E.2
  • 30
    • 78651457445 scopus 로고    scopus 로고
    • Oncogenic BRAF induces melanoma cell invasion by downregulating the cGMP-specific phosphodiesterase PDE5A
    • Arozarena I, Sanchez-Laorden B, Packer L, Hidalgo-Carcedo C, Hayward R, Viros A, et al. Oncogenic BRAF induces melanoma cell invasion by downregulating the cGMP-specific phosphodiesterase PDE5A. Cancer Cell 2011;19:45-57.
    • (2011) Cancer Cell , vol.19 , pp. 45-57
    • Arozarena, I.1    Sanchez-Laorden, B.2    Packer, L.3    Hidalgo-Carcedo, C.4    Hayward, R.5    Viros, A.6
  • 31
    • 0037205048 scopus 로고    scopus 로고
    • The phosphoinositide 3-kinase pathway
    • Cantley LC. The phosphoinositide 3-kinase pathway. Science 2002;296: 1655-7.
    • (2002) Science , vol.296 , pp. 1655-1657
    • Cantley, L.C.1
  • 32
    • 0035936783 scopus 로고    scopus 로고
    • NF1 tumor suppressor gene function: Narrowing the GAP
    • Cichowski K, Jacks T. NF1 tumor suppressor gene function: narrowing the GAP. Cell 2001;104:593-604.
    • (2001) Cell , vol.104 , pp. 593-604
    • Cichowski, K.1    Jacks, T.2
  • 33
    • 43049128529 scopus 로고    scopus 로고
    • Tenets of PTEN tumor suppression
    • Salmena L, Carracedo A, Pandolfi PP. Tenets of PTEN tumor suppression. Cell 2008;133:403-14.
    • (2008) Cell , vol.133 , pp. 403-414
    • Salmena, L.1    Carracedo, A.2    Pandolfi, P.P.3
  • 35
    • 0032533225 scopus 로고    scopus 로고
    • 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;12:3499-511.
    • (1998) Genes Dev , vol.12 , pp. 3499-3511
    • Diehl, J.A.1    Cheng, M.2    Roussel, M.F.3    Sherr, C.J.4
  • 36
    • 33750044112 scopus 로고    scopus 로고
    • Stress and mTORture signaling
    • Reiling JH, Sabatini DM. Stress and mTORture signaling. Oncogene 2006;25: 6373-83.
    • (2006) Oncogene , vol.25 , pp. 6373-6383
    • Reiling, J.H.1    Sabatini, D.M.2
  • 37
    • 3342895823 scopus 로고    scopus 로고
    • Rictor, a novel binding partner of mTOR, defines a rapamycin-insensi-tive and raptor-independent pathway that regulates the cytoskeleton
    • Sarbassov DD, Ali SM, Kim DH, Guertin DA, Latek RR, Erdjument-Bromage H, et al. Rictor, a novel binding partner of mTOR, defines a rapamycin-insensi-tive and raptor-independent pathway that regulates the cytoskeleton. Curr Biol 2004;14:1296-302.
    • (2004) Curr Biol , vol.14 , pp. 1296-1302
    • Sarbassov, D.D.1    Ali, S.M.2    Kim, D.H.3    Guertin, D.A.4    Latek, R.R.5    Erdjument-Bromage, H.6
  • 38
    • 63149194964 scopus 로고    scopus 로고
    • (V600E)BRAF is associated with disabled feedback inhibition of RAF-MEK signaling and elevated transcriptional output of the pathway
    • Pratilas CA, Taylor BS, Ye Q, Viale A, Sander C, Solit DB, et al. (V600E)BRAF is associated with disabled feedback inhibition of RAF-MEK signaling and elevated transcriptional output of the pathway. Proc Natl Acad Sci USA 2009;106:4519-24.
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 4519-4524
    • Pratilas, C.A.1    Taylor, B.S.2    Ye, Q.3    Viale, A.4    Sander, C.5    Solit, D.B.6
  • 40
    • 0033539167 scopus 로고    scopus 로고
    • Suppression of Raf-1 kinase activity and MAP kinase signalling by RKIP
    • Yeung K, Seitz T, Li S, Janosch P, McFerran B, Kaiser C, et al. Suppression of Raf-1 kinase activity and MAP kinase signalling by RKIP. Nature 1999;401:173-7.
    • (1999) Nature , vol.401 , pp. 173-177
    • Yeung, K.1    Seitz, T.2    Li, S.3    Janosch, P.4    McFerran, B.5    Kaiser, C.6
  • 42
    • 0037197949 scopus 로고    scopus 로고
    • MAP kinase module: The Ksr connection
    • Roy F, Therrien M. MAP kinase module: the Ksr connection. Curr Biol 2002;12:R325-7.
    • (2002) Curr Biol , vol.12 , pp. R325-R327
    • Roy, F.1    Therrien, M.2
  • 43
    • 84872818282 scopus 로고    scopus 로고
    • Dual-specificity MAP kinase phosphatases (MKPs): Shaping the outcome of MAP kinase signalling
    • Caunt CJ, Keyse SM. Dual-specificity MAP kinase phosphatases (MKPs): shaping the outcome of MAP kinase signalling. FEBS J 2013;280:489-504.
    • (2013) FEBS J , vol.280 , pp. 489-504
    • Caunt, C.J.1    Keyse, S.M.2
  • 44
    • 0035824694 scopus 로고    scopus 로고
    • Mammalian sprouty proteins inhibit cell growth and differentiation by preventing ras activation
    • Gross I, Bassit B, Benezra M, Licht JD. Mammalian sprouty proteins inhibit cell growth and differentiation by preventing ras activation. J Biol Chem 2001;276:46460-68.
    • (2001) J Biol Chem , vol.276 , pp. 46460-46468
    • Gross, I.1    Bassit, B.2    Benezra, M.3    Licht, J.D.4
  • 45
    • 70149094119 scopus 로고    scopus 로고
    • Sprouty2 association with B-Raf is regulated by phosphorylation and kinase confor-mation
    • Brady SC, Coleman ML, Munro J, Feller SM, Morrice NA, Olson MF. Sprouty2 association with B-Raf is regulated by phosphorylation and kinase confor-mation. Cancer Res 2009;69:6773-81.
    • (2009) Cancer Res , vol.69 , pp. 6773-6781
    • Brady, S.C.1    Coleman, M.L.2    Munro, J.3    Feller, S.M.4    Morrice, N.A.5    Olson, M.F.6
  • 46
    • 4143139997 scopus 로고    scopus 로고
    • SPRY2 is an inhibitor of the ras/extracellular signal-regulated kinase pathway in melanocytes and melanoma cells with wild-type BRAF but not with the V599E mutant
    • Tsavachidou D, Coleman ML, Athanasiadis G, Li S, Licht JD, Olson MF, et al. SPRY2 is an inhibitor of the ras/extracellular signal-regulated kinase pathway in melanocytes and melanoma cells with wild-type BRAF but not with the V599E mutant. Cancer Res 2004;64:5556-9.
    • (2004) Cancer Res , vol.64 , pp. 5556-5559
    • Tsavachidou, D.1    Coleman, M.L.2    Athanasiadis, G.3    Li, S.4    Licht, J.D.5    Olson, M.F.6
  • 47
    • 0034463918 scopus 로고    scopus 로고
    • A rapamycin-sensitive pathway down-regulates insulin signaling via phos-phorylation and proteasomal degradation of insulin receptor substrate-1
    • Haruta T, Uno T, Kawahara J, Takano A, Egawa K, Sharma PM, et al. A rapamycin-sensitive pathway down-regulates insulin signaling via phos-phorylation and proteasomal degradation of insulin receptor substrate-1. Mol Endocrinol 2000;14:783-94.
    • (2000) Mol Endocrinol , vol.14 , pp. 783-794
    • Haruta, T.1    Uno, T.2    Kawahara, J.3    Takano, A.4    Egawa, K.5    Sharma, P.M.6
  • 48
    • 0030780254 scopus 로고    scopus 로고
    • The IRS-signaling system: A network of docking proteins that mediate insulin and cytokine action
    • White MF, Yenush L. The IRS-signaling system: a network of docking proteins that mediate insulin and cytokine action. Curr Top Microbiol Immunol 1998;228:179-208.
    • (1998) Curr Top Microbiol Immunol , vol.228 , pp. 179-208
    • White, M.F.1    Yenush, L.2
  • 49
    • 0035155272 scopus 로고    scopus 로고
    • Serine/threonine phosphorylation of IRS-1 triggers its degradation: Possible regulation by tyrosine phosphor-ylation
    • Pederson TM, Kramer DL, Rondinone CM. Serine/threonine phosphorylation of IRS-1 triggers its degradation: possible regulation by tyrosine phosphor-ylation. Diabetes 2001;50:24-31.
    • (2001) Diabetes , vol.50 , pp. 24-31
    • Pederson, T.M.1    Kramer, D.L.2    Rondinone, C.M.3
  • 51
    • 32944457518 scopus 로고    scopus 로고
    • MTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt
    • O'reilly KE, Rojo F, She QB, Solit D, Mills GB, Smith D, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt. Cancer Res 2006;66:1500-8.
    • (2006) Cancer Res , vol.66 , 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
  • 53
    • 0036092268 scopus 로고    scopus 로고
    • KIT mutations are common in incidental gastrointestinal stromal tumors one centimeter or less in size
    • Corless CL, McGreevey L, Haley A, Town A, Heinrich MC. KIT mutations are common in incidental gastrointestinal stromal tumors one centimeter or less in size. Am J Pathol 2002;160:1567-72.
    • (2002) Am J Pathol , vol.160 , pp. 1567-1572
    • Corless, C.L.1    McGreevey, L.2    Haley, A.3    Town, A.4    Heinrich, M.C.5
  • 54
    • 0037087531 scopus 로고    scopus 로고
    • Inhibition of KIT tyrosine kinase activity: A novel molecular approach to the treatment of KIT-positive malignancies
    • Heinrich MC, Blanke CD, Druker BJ, Corless CL. Inhibition of KIT tyrosine kinase activity: a novel molecular approach to the treatment of KIT-positive malignancies. J Clin Oncol 2002;20:1692-703.
    • (2002) J Clin Oncol , vol.20 , pp. 1692-1703
    • Heinrich, M.C.1    Blanke, C.D.2    Druker, B.J.3    Corless, C.L.4
  • 55
    • 2342471392 scopus 로고    scopus 로고
    • Activating mutations in the epidermal growth factor receptor underly-ing responsiveness of non-small-cell lung cancer to gefitinib
    • Lynch TJ, Bell DW, Sordella R, Gurubhagavatula S, Okimoto RA, Brannigan BW, et al. Activating mutations in the epidermal growth factor receptor underly-ing responsiveness of non-small-cell lung cancer to gefitinib. N Engl J Med 2004;350:2129-39.
    • (2004) N Engl J Med , vol.350 , pp. 2129-2139
    • Lynch, T.J.1    Bell, D.W.2    Sordella, R.3    Gurubhagavatula, S.4    Okimoto, R.A.5    Brannigan, B.W.6
  • 56
    • 0035810147 scopus 로고    scopus 로고
    • Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia
    • Druker BJ, Talpaz M, Resta DJ, Peng B, Buchdunger E, Ford JM, et al. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N Engl J Med 2001;344:1031-7.
    • (2001) N Engl J Med , vol.344 , pp. 1031-1037
    • Druker, B.J.1    Talpaz, M.2    Resta, D.J.3    Peng, B.4    Buchdunger, E.5    Ford, J.M.6
  • 57
    • 51349164790 scopus 로고    scopus 로고
    • Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
    • Carracedo A, Ma L, Teruya-Feldstein J, Rojo F, Salmena L, Alimonti A, et al. Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer. J Clin Invest 2008;118: 3065-74.
    • (2008) J Clin Invest , vol.118 , pp. 3065-3074
    • Carracedo, A.1    Ma, L.2    Teruya-Feldstein, J.3    Rojo, F.4    Salmena, L.5    Alimonti, A.6
  • 58
    • 27644534999 scopus 로고    scopus 로고
    • 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;4:1533-40.
    • (2005) Mol Cancer Ther , vol.4 , pp. 1533-1540
    • Shi, Y.1    Yan, H.2    Frost, P.3    Gera, J.4    Lichtenstein, A.5
  • 59
    • 79958696694 scopus 로고    scopus 로고
    • The mTOR-regulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling
    • Hsu PP, Kang SA, Rameseder J, Zhang Y, Ottina KA, Lim D, et al. The mTOR-regulated phosphoproteome reveals a mechanism of mTORC1-mediated inhibition of growth factor signaling. Science 2011;332:1317-22.
    • (2011) Science , vol.332 , pp. 1317-1322
    • Hsu, P.P.1    Kang, S.A.2    Rameseder, J.3    Zhang, Y.4    Ottina, K.A.5    Lim, D.6
  • 60
    • 79958696336 scopus 로고    scopus 로고
    • Phosphopro-teomic analysis identifies Grb10 as an mTORC1 substrate that negatively regulates insulin signaling
    • Yu Y, Yoon SO, Poulogiannis G, Yang Q, Ma XM, Villen J, et al. Phosphopro-teomic analysis identifies Grb10 as an mTORC1 substrate that negatively regulates insulin signaling. Science 2011;332:1322-6.
    • (2011) Science , vol.332 , pp. 1322-1326
    • Yu, Y.1    Yoon, S.O.2    Poulogiannis, G.3    Yang, Q.4    Ma, X.M.5    Villen, J.6
  • 61
    • 42949095922 scopus 로고    scopus 로고
    • Constitutive activation of the Raf-MAPK pathway causes negative feedback inhibition of Ras-PI3K-AKT and cellular arrest through the EphA2 receptor
    • Menges CW, McCance DJ. Constitutive activation of the Raf-MAPK pathway causes negative feedback inhibition of Ras-PI3K-AKT and cellular arrest through the EphA2 receptor. Oncogene 2008;27:2934-40.
    • (2008) Oncogene , vol.27 , pp. 2934-2940
    • Menges, C.W.1    McCance, D.J.2
  • 64
    • 33846552656 scopus 로고    scopus 로고
    • Escape from HER-family tyrosine kinase inhibitor therapy by the kinase-inactive HER3
    • Sergina NV, Rausch M, Wang D, Blair J, Hann B, Shokat KM, et al. Escape from HER-family tyrosine kinase inhibitor therapy by the kinase-inactive HER3. Nature 2007;445:437-41.
    • (2007) Nature , vol.445 , pp. 437-441
    • Sergina, N.V.1    Rausch, M.2    Wang, D.3    Blair, J.4    Hann, B.5    Shokat, K.M.6
  • 65
    • 34347369084 scopus 로고    scopus 로고
    • Post-translational modifications and regulation of the RAS superfamily of GTPases as anticancer targets
    • Konstantinopoulos PA, Karamouzis MV, Papavassiliou AG. Post-translational modifications and regulation of the RAS superfamily of GTPases as anticancer targets. Nat Rev Drug Discov 2007;6:541-55.
    • (2007) Nat Rev Drug Discov , vol.6 , pp. 541-555
    • Konstantinopoulos, P.A.1    Karamouzis, M.V.2    Papavassiliou, A.G.3
  • 66
    • 84888639050 scopus 로고    scopus 로고
    • K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions
    • Ostrem JM, Peters U, Sos ML, Wells JA, Shokat KM. K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions. Nature 2013;503: 548-51.
    • (2013) Nature , vol.503 , pp. 548-551
    • Ostrem, J.M.1    Peters, U.2    Sos, M.L.3    Wells, J.A.4    Shokat, K.M.5
  • 67
    • 84878401236 scopus 로고    scopus 로고
    • Small molecule inhibition of the KRAS-PDEdelta interaction impairs onco-genic KRAS signalling
    • Zimmermann G, Papke B, Ismail S, Vartak N, Chandra A, Hoffmann M, et al. Small molecule inhibition of the KRAS-PDEdelta interaction impairs onco-genic KRAS signalling. Nature 2013;497:638-42.
    • (2013) Nature , vol.497 , pp. 638-642
    • Zimmermann, G.1    Papke, B.2    Ismail, S.3    Vartak, N.4    Chandra, A.5    Hoffmann, M.6
  • 68
    • 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
  • 69
    • 0037454224 scopus 로고    scopus 로고
    • Mutations in BRAF and KRAS characterize the development of low-grade ovarian serous carcinoma
    • Singer G, Oldt 3rd R, Cohen Y, Wang BG, Sidransky D, Kurman RJ, et al. Mutations in BRAF and KRAS characterize the development of low-grade ovarian serous carcinoma. J Natl Cancer Inst 2003;95:484-6.
    • (2003) J Natl Cancer Inst , vol.95 , pp. 484-486
    • Singer, G.1    Oldt, R.2    Cohen, Y.3    Wang, B.G.4    Sidransky, D.5    Kurman, R.J.6
  • 72
    • 84863230465 scopus 로고    scopus 로고
    • Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feed-back activation of EGFR
    • Prahallad A, Sun C, Huang S, Di Nicolantonio F, Salazar R, Zecchin D, et al. Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feed-back activation of EGFR. Nature 2012;483:100-3.
    • (2012) Nature , vol.483 , pp. 100-103
    • Prahallad, A.1    Sun, C.2    Huang, S.3    Di Nicolantonio, F.4    Salazar, R.5    Zecchin, D.6
  • 73
    • 42949149240 scopus 로고    scopus 로고
    • Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity
    • Tsai J, Lee JT, Wang W, Zhang J, Cho H, Mamo S, et al. Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc Natl Acad Sci USA 2008;105:3041-6.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 3041-3046
    • Tsai, J.1    Lee, J.T.2    Wang, W.3    Zhang, J.4    Cho, H.5    Mamo, S.6
  • 74
    • 33845730781 scopus 로고    scopus 로고
    • Demonstration of a genetic therapeutic index for tumors expressing oncogenic BRAF by the kinase inhibitor SB-590885
    • King AJ, Patrick DR, Batorsky RS, Ho ML, Do HT, Zhang SY, et al. Demonstration of a genetic therapeutic index for tumors expressing oncogenic BRAF by the kinase inhibitor SB-590885. Cancer Res 2006;66:11100-05.
    • (2006) Cancer Res , vol.66 , pp. 11100-11105
    • King, A.J.1    Patrick, D.R.2    Batorsky, R.S.3    Ho, M.L.4    Do, H.T.5    Zhang, S.Y.6
  • 75
    • 84896757312 scopus 로고    scopus 로고
    • Targeting ER stress-induced autophagy overcomes BRAF inhibitor resistance in melanoma
    • Ma XH, Piao SF, Dey S, McAfee Q, Karakousis G, Villanueva J, et al. Targeting ER stress-induced autophagy overcomes BRAF inhibitor resistance in melanoma. J Clin Invest 2014;124:1406-17.
    • (2014) J Clin Invest , vol.124 , pp. 1406-1417
    • Ma, X.H.1    Piao, S.F.2    Dey, S.3    McAfee, Q.4    Karakousis, G.5    Villanueva, J.6
  • 76
    • 77956513286 scopus 로고    scopus 로고
    • Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma
    • Bollag G, Hirth P, Tsai J, Zhang J, Ibrahim PN, Cho H, et al. Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma. Nature 2010;467:596-9.
    • (2010) Nature , vol.467 , pp. 596-599
    • Bollag, G.1    Hirth, P.2    Tsai, J.3    Zhang, J.4    Ibrahim, P.N.5    Cho, H.6
  • 77
    • 84891898344 scopus 로고    scopus 로고
    • 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
  • 78
    • 77953276524 scopus 로고    scopus 로고
    • Recovery of phospho-ERK activity allows melanoma cells to escape from BRAF inhibitor therapy
    • Paraiso KH, Fedorenko IV, Cantini LP, Munko AC, Hall M, Sondak VK, et al. Recovery of phospho-ERK activity allows melanoma cells to escape from BRAF inhibitor therapy. Br J Cancer 2010;102:1724-30.
    • (2010) Br J Cancer , vol.102 , pp. 1724-1730
    • Paraiso, K.H.1    Fedorenko, I.V.2    Cantini, L.P.3    Munko, A.C.4    Hall, M.5    Sondak, V.K.6
  • 79
    • 84869067183 scopus 로고    scopus 로고
    • Relief of profound feedback inhibition of mitogenic signaling by RAF inhibitors attenuates their activity in BRAFV600E melanomas
    • Lito P, Pratilas CA, Joseph EW, Tadi M, Halilovic E, Zubrowski M, et al. Relief of profound feedback inhibition of mitogenic signaling by RAF inhibitors attenuates their activity in BRAFV600E melanomas. Cancer Cell 2012;22: 668-82.
    • (2012) Cancer Cell , vol.22 , pp. 668-682
    • Lito, P.1    Pratilas, C.A.2    Joseph, E.W.3    Tadi, M.4    Halilovic, E.5    Zubrowski, M.6
  • 80
    • 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
  • 81
    • 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
  • 82
    • 84861381332 scopus 로고    scopus 로고
    • Adaptive upregulation of FOXD3 and resistance to PLX4032/4720-induced cell death in mutant B-RAF melanoma cells
    • Basile KJ, Abel EV, Aplin AE. Adaptive upregulation of FOXD3 and resistance to PLX4032/4720-induced cell death in mutant B-RAF melanoma cells. Onco-gene 2012;31(19):2471-9.
    • (2012) Onco-gene , vol.31 , Issue.19 , pp. 2471-2479
    • Basile, K.J.1    Abel, E.V.2    Aplin, A.E.3
  • 85
    • 84859765844 scopus 로고    scopus 로고
    • Dynamic reprogramming of the kinome in response to targeted MEK inhibition in triple-negative breast cancer
    • Duncan JS, Whittle MC, Nakamura K, Abell AN, Midland AA, Zawistowski JS, et al. Dynamic reprogramming of the kinome in response to targeted MEK inhibition in triple-negative breast cancer. Cell 2012;149:307-21.
    • (2012) Cell , vol.149 , pp. 307-321
    • Duncan, J.S.1    Whittle, M.C.2    Nakamura, K.3    Abell, A.N.4    Midland, A.A.5    Zawistowski, J.S.6
  • 86
    • 84873360893 scopus 로고    scopus 로고
    • Resistance to BRAF inhibition in BRAF-mutant colon cancer can be overcome with PI3K inhibition or demethylating agents
    • Mao M, Tian F, Mariadason JM, Tsao CC, Lemos Jr R, Dayyani F, et al. Resistance to BRAF inhibition in BRAF-mutant colon cancer can be overcome with PI3K inhibition or demethylating agents. Clin Cancer Res 2013;19:657-67.
    • (2013) Clin Cancer Res , vol.19 , pp. 657-667
    • Mao, M.1    Tian, F.2    Mariadason, J.M.3    Tsao, C.C.4    Lemos, R.5    Dayyani, F.6
  • 87
    • 84877631604 scopus 로고    scopus 로고
    • Relief of feedback inhibition of HER3 transcription by RAF and MEK inhibitors attenuates their antitumor effects in BRAF-mutant thyroid carci-nomas
    • Montero-Conde C, Ruiz-Llorente S, Dominguez JM, Knauf JA, Viale A, Sherman EJ, et al. Relief of feedback inhibition of HER3 transcription by RAF and MEK inhibitors attenuates their antitumor effects in BRAF-mutant thyroid carci-nomas. Cancer Discov 2013;3:520-33.
    • (2013) Cancer Discov , vol.3 , pp. 520-533
    • Montero-Conde, C.1    Ruiz-Llorente, S.2    Dominguez, J.M.3    Knauf, J.A.4    Viale, A.5    Sherman, E.J.6
  • 88
    • 84864285794 scopus 로고    scopus 로고
    • Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion
    • Straussman R, Morikawa T, Shee K, Barzily-Rokni M, Qian ZR, Du JY, et al. Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion. Nature 2012;487. 500-U118.
    • (2012) Nature , vol.487 , pp. 500-U118
    • Straussman, R.1    Morikawa, T.2    Shee, K.3    Barzily-Rokni, M.4    Qian, Z.R.5    Du, J.Y.6
  • 89
    • 84863336092 scopus 로고    scopus 로고
    • Paracrine receptor activation by microenvironment triggers bypass survival signals and ALK inhibitor resistance in EML4-ALK lung cancer cells
    • Yamada T, Takeuchi S, Nakade J, Kita K, Nakagawa T, Nanjo S, et al. Paracrine receptor activation by microenvironment triggers bypass survival signals and ALK inhibitor resistance in EML4-ALK lung cancer cells. Clin Cancer Res 2012;18:3592-602.
    • (2012) Clin Cancer Res , vol.18 , pp. 3592-3602
    • Yamada, T.1    Takeuchi, S.2    Nakade, J.3    Kita, K.4    Nakagawa, T.5    Nanjo, S.6
  • 91
    • 84891899026 scopus 로고    scopus 로고
    • MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibition
    • Wagle N, Van Allen EM, Treacy DJ, Frederick DT, Cooper ZA, Taylor-Weiner A, et al. MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibition. Cancer Discov 2014;4:61-8.
    • (2014) Cancer Discov , vol.4 , pp. 61-68
    • Wagle, N.1    Van Allen, E.M.2    Treacy, D.J.3    Frederick, D.T.4    Cooper, Z.A.5    Taylor-Weiner, A.6
  • 92
    • 79960985354 scopus 로고    scopus 로고
    • HSP90 inhibition is effective in breast cancer: A phase II trial of tanespimycin (17-AAG) plus trastuzumab in patients with HER2-positive metastatic breast cancer progressing on trastuzumab
    • Modi S, Stopeck A, Linden H, Solit D, Chandarlapaty S, Rosen N, et al. HSP90 inhibition is effective in breast cancer: a phase II trial of tanespimycin (17-AAG) plus trastuzumab in patients with HER2-positive metastatic breast cancer progressing on trastuzumab. Clin Cancer Res 2011;17:5132-9.
    • (2011) Clin Cancer Res , vol.17 , pp. 5132-5139
    • Modi, S.1    Stopeck, A.2    Linden, H.3    Solit, D.4    Chandarlapaty, S.5    Rosen, N.6
  • 93
    • 79957539428 scopus 로고    scopus 로고
    • Tanespimycin and bortezomib combination treatment in patients with relapsed or relapsed and refractory multiple myeloma: Results of a phase 1/2 study
    • Richardson PG, Chanan-Khan AA, Lonial S, Krishnan AY, Carroll MP, Alsina M, et al. Tanespimycin and bortezomib combination treatment in patients with relapsed or relapsed and refractory multiple myeloma: results of a phase 1/2 study. Br J Haematol 2011;153:729-40.
    • (2011) Br J Haematol , vol.153 , pp. 729-740
    • Richardson, P.G.1    Chanan-Khan, A.A.2    Lonial, S.3    Krishnan, A.Y.4    Carroll, M.P.5    Alsina, M.6
  • 94
    • 79960085862 scopus 로고    scopus 로고
    • Optimization of dosing for EGFR-mutant non-small cell lung cancer with evolutionary cancer modeling
    • Chmielecki J, Foo J, Oxnard GR, Hutchinson K, Ohashi K, Somwar R, et al. Optimization of dosing for EGFR-mutant non-small cell lung cancer with evolutionary cancer modeling. Sci Transl Med 2011;3:90ra59.
    • (2011) Sci Transl Med , vol.3 , pp. 90ra59
    • Chmielecki, J.1    Foo, J.2    Oxnard, G.R.3    Hutchinson, K.4    Ohashi, K.5    Somwar, R.6
  • 95
    • 44649083135 scopus 로고    scopus 로고
    • Hsp90 inhibition suppresses mutant EGFR-T790M signaling and overcomes kinase inhibitor resistance
    • Shimamura T, Li D, Ji H, Haringsma HJ, Liniker E, Borgman CL, et al. Hsp90 inhibition suppresses mutant EGFR-T790M signaling and overcomes kinase inhibitor resistance. Cancer Res 2008;68:5827-38.
    • (2008) Cancer Res , vol.68 , pp. 5827-5838
    • Shimamura, T.1    Li, D.2    Ji, H.3    Haringsma, H.J.4    Liniker, E.5    Borgman, C.L.6
  • 96
    • 84860533156 scopus 로고    scopus 로고
    • The HSP90 inhibitor XL888 overcomes BRAF inhibitor resistance mediated through diverse mechanisms
    • Paraiso KHT, Haarberg HE, Wood E, Rebecca VW, Chen YA, Xiang Y, et al. The HSP90 inhibitor XL888 overcomes BRAF inhibitor resistance mediated through diverse mechanisms. Clin Cancer Res 2012;18:2502-14.
    • (2012) Clin Cancer Res , vol.18 , pp. 2502-2514
    • Paraiso, K.H.T.1    Haarberg, H.E.2    Wood, E.3    Rebecca, V.W.4    Chen, Y.A.5    Xiang, Y.6
  • 97
    • 84873911646 scopus 로고    scopus 로고
    • Activity of the heat shock protein 90 inhibitor ganetespib in melanoma
    • Wu X, Marmarelis ME, Hodi FS. Activity of the heat shock protein 90 inhibitor ganetespib in melanoma. PLOS ONE 2013;8:e56134.
    • (2013) PLOS ONE , vol.8
    • Wu, X.1    Marmarelis, M.E.2    Hodi, F.S.3
  • 98
    • 84894183166 scopus 로고    scopus 로고
    • Overcom-ing acquired BRAF inhibitor resistance in melanoma via targeted inhibition of Hsp90 with ganetespib
    • Acquaviva J, Smith DL, Jimenez JP, Zhang C, Sequeira M, He S, et al. Overcom-ing acquired BRAF inhibitor resistance in melanoma via targeted inhibition of Hsp90 with ganetespib. Mol Cancer Ther 2014;13:353-63.
    • (2014) Mol Cancer Ther , vol.13 , pp. 353-363
    • Acquaviva, J.1    Smith, D.L.2    Jimenez, J.P.3    Zhang, C.4    Sequeira, M.5    He, S.6
  • 99
    • 84900442808 scopus 로고    scopus 로고
    • Disruption of CRAF-mediated MEK activation is required for effective MEK inhibition in KRAS mutant tumors
    • Lito P, Saborowski A, Yue J, Solomon M, Joseph E, Gadal S, et al. Disruption of CRAF-mediated MEK activation is required for effective MEK inhibition in KRAS mutant tumors. Cancer Cell 2014;25(5):697-710.
    • (2014) Cancer Cell , vol.25 , Issue.5 , pp. 697-710
    • Lito, P.1    Saborowski, A.2    Yue, J.3    Solomon, M.4    Joseph, E.5    Gadal, S.6
  • 100
    • 84880064248 scopus 로고    scopus 로고
    • Enhanced inhibition of ERK signaling by a novel allosteric MEK inhibitor, CH5126766, that suppresses feedback reactivation of RAF activity
    • Ishii N, Harada N, Joseph EW, Ohara K, Miura T, Sakamoto H, et al. Enhanced inhibition of ERK signaling by a novel allosteric MEK inhibitor, CH5126766, that suppresses feedback reactivation of RAF activity. Cancer Res 2013;73: 4050-60.
    • (2013) Cancer Res , vol.73 , pp. 4050-4060
    • Ishii, N.1    Harada, N.2    Joseph, E.W.3    Ohara, K.4    Miura, T.5    Sakamoto, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.