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Volumn 8, Issue 12, 2009, Pages 3296-3306

Targeting heat shock protein 90 with CUDC-305 overcomes erlotinib resistance in non-small cell lung cancer

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CUDC 305; EPIDERMAL GROWTH FACTOR RECEPTOR; ERLOTINIB; HEAT SHOCK PROTEIN 90; HEAT SHOCK PROTEIN 90 INHIBITOR; K RAS PROTEIN; MUTANT PROTEIN; ONCOPROTEIN; PACLITAXEL; UNCLASSIFIED DRUG;

EID: 73149093419     PISSN: 15357163     EISSN: None     Source Type: Journal    
DOI: 10.1158/1535-7163.MCT-09-0538     Document Type: Article
Times cited : (54)

References (37)
  • 1
    • 0003964363 scopus 로고    scopus 로고
    • Available from
    • American Cancer Society. Cancer facts & figures 2008. Available from: http://www.cancer.org/downloads/STT/2008CAFFfinalsecured.pdf.
    • (2008) Cancer facts & figures
  • 2
    • 28444468144 scopus 로고    scopus 로고
    • Rodriquez . EGFR inhibitors: What have we learned from the treatment of lung cancer? Nat Clin Pract
    • Giaccone G, Rodriquez . EGFR inhibitors: what have we learned from the treatment of lung cancer? Nat Clin Pract Oncol 2005;2:554-61.
    • (2005) Oncol , vol.2 , pp. 554-561
    • Giaccone, G.1
  • 3
    • 2342471392 scopus 로고    scopus 로고
    • Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib
    • Lynch TJ, Bell DW, Sordella R, et al. Activating mutations in the epidermal growth factor receptor underlying 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
  • 4
    • 2342624080 scopus 로고    scopus 로고
    • EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
    • Paez JG, Jänne PA, Lee JC, et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 2004;304:1497-500.
    • (2004) Science , vol.304 , pp. 1497-1500
    • Paez, J.G.1    Jänne, P.A.2    Lee, J.C.3
  • 5
    • 4444344330 scopus 로고    scopus 로고
    • EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib
    • Pao W, Miller V, Zakowski M, et al. EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci U S A 2004;101:13306-11.
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 13306-13311
    • Pao, W.1    Miller, V.2    Zakowski, M.3
  • 6
    • 4143066760 scopus 로고    scopus 로고
    • Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways
    • Sordella R, Bell DW, Haber DA, Settleman J. Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways. Science 2004;305:1163-7.
    • (2004) Science , vol.305 , pp. 1163-1167
    • Sordella, R.1    Bell, D.W.2    Haber, D.A.3    Settleman, J.4
  • 7
    • 17144395523 scopus 로고    scopus 로고
    • Inhibition of mutant EGF receptors by gefitinib: Targeting an Achilles' heel of lung cancer
    • Settleman J. Inhibition of mutant EGF receptors by gefitinib: targeting an Achilles' heel of lung cancer. Cell Cycle 2004;3:1496-7.
    • (2004) Cell Cycle , vol.3 , pp. 1496-1497
    • Settleman, J.1
  • 9
    • 18244371651 scopus 로고    scopus 로고
    • Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
    • Pao W, Miller VA, Politi KA, et al. Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS Med 2005;2:225-35.
    • (2005) PLoS Med , vol.2 , pp. 225-235
    • Pao, W.1    Miller, V.A.2    Politi, K.A.3
  • 10
    • 23344440655 scopus 로고    scopus 로고
    • Inhibition of drug-resistant mutants of ABL, KIT, EGF receptor kinases
    • Carter TA, Wodicka LM, Shah NP, et al. Inhibition of drug-resistant mutants of ABL, KIT, EGF receptor kinases. Proc Natl Acad Sci U S A 2005;102:11011-6.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , pp. 11011-11016
    • Carter, T.A.1    Wodicka, L.M.2    Shah, N.P.3
  • 11
    • 40049099220 scopus 로고    scopus 로고
    • The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP
    • Yun C, Mengwasser KE, Toms AV, et al. The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc Natl Acad Sci U S A 2008;105:2070-5.
    • (2008) Proc Natl Acad Sci U S A , vol.105 , pp. 2070-2075
    • Yun, C.1    Mengwasser, K.E.2    Toms, A.V.3
  • 12
    • 21144439000 scopus 로고    scopus 로고
    • Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib
    • Kwak EL, Sordella R, Bell DW, et al. Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib. Proc Natl Acad Sci U S A 2005;102:7665-70.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , pp. 7665-7670
    • Kwak, E.L.1    Sordella, R.2    Bell, D.W.3
  • 13
    • 33744824672 scopus 로고    scopus 로고
    • Phase I study of EKB-569, an irreversible inhibitor of the epidermal growth factor receptor, in patients with advanced solid tumors
    • Erlichman C, Hidalgo M, Boni JP, et al. Phase I study of EKB-569, an irreversible inhibitor of the epidermal growth factor receptor, in patients with advanced solid tumors. J Clin Oncol 2006;24:2252-60.
    • (2006) J Clin Oncol , vol.24 , pp. 2252-2260
    • Erlichman, C.1    Hidalgo, M.2    Boni, J.P.3
  • 14
    • 2542582261 scopus 로고    scopus 로고
    • Antitumor activity of HKI-272, an orally active, irreversible inhibitor of the HER-2 tyrosine kinase
    • Rabindran SK, Discafani CM, Rosfjord EC, et al. Antitumor activity of HKI-272, an orally active, irreversible inhibitor of the HER-2 tyrosine kinase. Cancer Res 2004;64:3958-65.
    • (2004) Cancer Res , vol.64 , pp. 3958-3965
    • Rabindran, S.K.1    Discafani, C.M.2    Rosfjord, E.C.3
  • 15
    • 0033561601 scopus 로고    scopus 로고
    • Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with in vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785)
    • Discafani CM, Carroll ML, Floyd MB, Jr., et al. Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with in vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785). Biochem Pharmacol 1999;57:917-25.
    • (1999) Biochem Pharmacol , vol.57 , pp. 917-925
    • Discafani, C.M.1    Carroll, M.L.2    Floyd Jr., M.B.3
  • 16
    • 0034611617 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors: 17. Irreversible inhibitors of the epidermal growth factor receptor-4-(phenylamino) quinazoline-and 4-(phenylamino)pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
    • Smaill JB, Rewcastle GW, Loo JA, et al. Tyrosine kinase inhibitors: 17. Irreversible inhibitors of the epidermal growth factor receptor-4-(phenylamino) quinazoline-and 4-(phenylamino)pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions. J Med Chem 2000;43:1380-97.
    • (2000) J Med Chem , vol.43 , pp. 1380-1397
    • Smaill, J.B.1    Rewcastle, G.W.2    Loo, J.A.3
  • 17
    • 34547749490 scopus 로고    scopus 로고
    • HKI-272 in non-small cell lung cancer
    • s
    • Wong KK. HKI-272 in non-small cell lung cancer. Clin Cancer Res 2007;13:4593-6s.
    • (2007) Clin Cancer Res , vol.13 , pp. 4593-4596
    • Wong, K.K.1
  • 18
    • 34347208648 scopus 로고    scopus 로고
    • Bronchial and peripheral murine lung carcinomas induced by T790M-L858R mutant EGFR respond to HKI-272 and rapamycin combination therapy
    • Li D, Shimamura T, Ji H, et al. Bronchial and peripheral murine lung carcinomas induced by T790M-L858R mutant EGFR respond to HKI-272 and rapamycin combination therapy. Cancer Cell 2007;12:6-8.
    • (2007) Cancer Cell , vol.12 , pp. 6-8
    • Li, D.1    Shimamura, T.2    Ji, H.3
  • 19
    • 34249075147 scopus 로고    scopus 로고
    • MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
    • Engelman JA, Zejnullahu K, Mitsudomi T, et al. MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 2007;316:1039-43.
    • (2007) Science , vol.316 , pp. 1039-1043
    • Engelman, J.A.1    Zejnullahu, K.2    Mitsudomi, T.3
  • 20
    • 38049150665 scopus 로고    scopus 로고
    • MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib
    • Bean J, Brennan C, Shih J, et al. MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib. Proc Natl Acad Sci U S A 2007;104:20932-7.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 20932-20937
    • Bean, J.1    Brennan, C.2    Shih, J.3
  • 21
    • 34249810645 scopus 로고    scopus 로고
    • KRAS mutation is an important predictor of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in non-small-cell lung cancer
    • Massarelli E, Varella-Garcia M, Tang X, et al. KRAS mutation is an important predictor of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in non-small-cell lung cancer. Clin Cancer Res 2007;13:2890-6.
    • (2007) Clin Cancer Res , vol.13 , pp. 2890-2896
    • Massarelli, E.1    Varella-Garcia, M.2    Tang, X.3
  • 22
    • 15744372810 scopus 로고    scopus 로고
    • KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib
    • Pao W, Wang TY, Riely GJ, et al. KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. PLoS Med 2005;2:e17.
    • (2005) PLoS Med , vol.2
    • Pao, W.1    Wang, T.Y.2    Riely, G.J.3
  • 23
    • 21244500107 scopus 로고    scopus 로고
    • Mutational analysis of EGFR and K-RAS genes in lung adenocarcinomas
    • Song YH, Lee JW, Kim SY, et al. Mutational analysis of EGFR and K-RAS genes in lung adenocarcinomas. Virchows Arch 2005;446:483-8.
    • (2005) Virchows Arch , vol.446 , pp. 483-488
    • Song, Y.H.1    Lee, J.W.2    Kim, S.Y.3
  • 24
    • 0037616593 scopus 로고    scopus 로고
    • Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors
    • Bianco R, Shin I, Ritter CA, et al. Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors. Oncogene 2003;22:2812-22.
    • (2003) Oncogene , vol.22 , pp. 2812-2822
    • Bianco, R.1    Shin, I.2    Ritter, C.A.3
  • 25
    • 25844481618 scopus 로고    scopus 로고
    • Ciardiello . Intrinsic and acquired resistance to EGFR inhibitors in human cancer therapy
    • Bianco R, Troiani T, Tortora G, Ciardiello . Intrinsic and acquired resistance to EGFR inhibitors in human cancer therapy. Endocr Relat Cancer 2005;12:S159-71.
    • (2005) Endocr Relat Cancer , vol.12
    • Bianco, R.1    Troiani, T.2    Tortora, G.3
  • 26
    • 0035989680 scopus 로고    scopus 로고
    • HSP90 as a new therapeutic target for cancer therapy: The story unfolds
    • Maloney A, Workman P. HSP90 as a new therapeutic target for cancer therapy: the story unfolds. Expert Opin Biol Ther 2002;2:3-24.
    • (2002) Expert Opin Biol Ther , vol.2 , pp. 3-24
    • Maloney, A.1    Workman, P.2
  • 27
    • 35348890981 scopus 로고    scopus 로고
    • Drugging the cancer chaperone HSP90: Combinatorial therapeutic exploitation of oncogene addiction and tumor stress
    • Workman P, Burrows F, Neckers L, Rosen N. Drugging the cancer chaperone HSP90: combinatorial therapeutic exploitation of oncogene addiction and tumor stress. Ann N Y Acad Sci 2007;1113:202-16.
    • (2007) Ann N Y Acad Sci , vol.1113 , pp. 202-216
    • Workman, P.1    Burrows, F.2    Neckers, L.3    Rosen, N.4
  • 28
    • 67449138839 scopus 로고    scopus 로고
    • CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacological properties for cancer therapy
    • Bao R, Lai C, Qu H, et al. CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacological properties for cancer therapy. Clin Cancer Res 2009;15:4046-57.
    • (2009) Clin Cancer Res , vol.15 , pp. 4046-4057
    • Bao, R.1    Lai, C.2    Qu, H.3
  • 29
    • 0033813922 scopus 로고    scopus 로고
    • Use of a surrogate marker (human secreted alkaline phosphatase) to monitor in vivo tumor growth and anticancer drug efficacy in ovarian cancer xenografts
    • Bao R, Selvakumaran M, Hamilton TC. Use of a surrogate marker (human secreted alkaline phosphatase) to monitor in vivo tumor growth and anticancer drug efficacy in ovarian cancer xenografts. Gynecol Oncol 2000;78:373-9.
    • (2000) Gynecol Oncol , vol.78 , pp. 373-379
    • Bao, R.1    Selvakumaran, M.2    Hamilton, T.C.3
  • 30
    • 13944256060 scopus 로고    scopus 로고
    • Human tumor xenograft models in NCI drug development
    • Teicher BA, Andrews PA, editors, New Jersey: Humana Press, Inc
    • Alley MC, Hollingshead MG, Dykes DJ, Waud WR. Human tumor xenograft models in NCI drug development. In: Teicher BA, Andrews PA, editors. Anticancer drug development guide. New Jersey: Humana Press, Inc.; 2004, p. 125-52.
    • (2004) Anticancer drug development guide , pp. 125-152
    • Alley, M.C.1    Hollingshead, M.G.2    Dykes, D.J.3    Waud, W.R.4
  • 31
    • 49449112267 scopus 로고    scopus 로고
    • Effect of lapatinib on the outgrowth of metastatic breast cancer cells to brain
    • Gril B, Palmieri D, Bronder JL, et al. Effect of lapatinib on the outgrowth of metastatic breast cancer cells to brain. J Natl Cancer Inst 2008;100:1092-103.
    • (2008) J Natl Cancer Inst , vol.100 , pp. 1092-1103
    • Gril, B.1    Palmieri, D.2    Bronder, J.L.3
  • 32
    • 73149107848 scopus 로고    scopus 로고
    • Curis Inc., assignee. Fused aminopyridine as HSP90 inhibitors. World Intellectual Property Organization
    • WO /115719 A1. 2008 Sept 25
    • Cai X, Qian C, Zhai H, inventors; Curis Inc., assignee. Fused aminopyridine as HSP90 inhibitors. World Intellectual Property Organization WO 2008/115719 A1. 2008 Sept 25.
    • (2008)
    • Cai, X.1    Qian, C.2    Zhai, H.3    inventors4
  • 33
    • 44649083135 scopus 로고    scopus 로고
    • Hsp90 inhibition suppresses mutant EGFR-T790M signaling and overcomes kinase inhibitor resistance
    • Shimamura T, Li D, Ji H, 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
  • 34
    • 22244485706 scopus 로고    scopus 로고
    • Epidermal growth factor receptors harboring kinase domain mutations associate with the heat shock protein 90 chaperone and are destabilized following exposure to geldanamycins
    • Shimamura T, Lowell AM, Engelman JA, Shapiro GI. Epidermal growth factor receptors harboring kinase domain mutations associate with the heat shock protein 90 chaperone and are destabilized following exposure to geldanamycins. Cancer Res 2005;64:6401-8.
    • (2005) Cancer Res , vol.64 , pp. 6401-6408
    • Shimamura, T.1    Lowell, A.M.2    Engelman, J.A.3    Shapiro, G.I.4
  • 35
    • 0029740191 scopus 로고    scopus 로고
    • Nussbaum ES, Djalilian HR, Cho KH, Hall WA. Brain metastases. Histology, multiplicity, surgery, and survival. Cancer 1996;78:1781-8.
    • Nussbaum ES, Djalilian HR, Cho KH, Hall WA. Brain metastases. Histology, multiplicity, surgery, and survival. Cancer 1996;78:1781-8.
  • 36
    • 73149121457 scopus 로고    scopus 로고
    • Münster PN, Basso A, Solit D. Modulation of Hsp90 function by ansamycins sensitizes breast cancer cells to chemotherapy-induced apoptosis in an RB- and schedule-dependent manner. See the Biology Behind: E. A. Sausville, Combining cytotoxics and 17-allylamino, 17-demethoxygeldanamycin: sequence and tumor biology matters. Clin Cancer Res 2001;7:2155-8.
    • Münster PN, Basso A, Solit D. Modulation of Hsp90 function by ansamycins sensitizes breast cancer cells to chemotherapy-induced apoptosis in an RB- and schedule-dependent manner. See the Biology Behind: E. A. Sausville, Combining cytotoxics and 17-allylamino, 17-demethoxygeldanamycin: sequence and tumor biology matters. Clin Cancer Res 2001;7:2155-8.
  • 37
    • 49649127657 scopus 로고    scopus 로고
    • Mechanisms of acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer
    • Engelman JA, Janne PA. Mechanisms of acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancer. Clin Cancer Res 14:2895-9.
    • Clin Cancer Res , vol.14 , pp. 2895-2899
    • Engelman, J.A.1    Janne, P.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.