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Volumn 23, Issue 5, 2014, Pages 611-628

Heat shock protein 90 inhibitors in the treatment of cancer: Current status and future directions

Author keywords

Cancer; Clinical development; Heat shock protein 90 inhibitors; Patient selection

Indexed keywords

ABIRATERONE; ALVESPIMYCIN; AT 13387; BENZOQUINONE; BIIB 021; BORTEZOMIB; CETUXIMAB; CNF 2024; CRIZOTINIB; CUDC 305; DEBIO 0932; DOCETAXEL; ERLOTINIB; EVEROLIMUS; GANETESPIB; GELDANAMYCIN; HEAT SHOCK PROTEIN 90; HEAT SHOCK PROTEIN 90 INHIBITOR; HSP 990; IMATINIB; KW 2478; LUMINESPIB; MPC 3100; NVP HSP 990; PU H 71; RESORCINOL; RETASPIMYCIN; SNX 5422; TANESPIMYCIN; TRASTUZUMAB; UNCLASSIFIED DRUG; UNINDEXED DRUG; VER 52269; XL 888; ANTINEOPLASTIC AGENT;

EID: 84898447762     PISSN: 13543784     EISSN: 17447658     Source Type: Journal    
DOI: 10.1517/13543784.2014.902442     Document Type: Review
Times cited : (141)

References (99)
  • 1
    • 75149177573 scopus 로고    scopus 로고
    • Hsp90 and co-chaperones twist the functions of diverse client proteins
    • Zuehlke A, Johnson JL. Hsp90 and co-chaperones twist the functions of diverse client proteins. Biopolymers 2010;93(3):211-17
    • (2010) Biopolymers , vol.93 , Issue.3 , pp. 211-217
    • Zuehlke, A.1    Johnson, J.L.2
  • 2
    • 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, et al. 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
  • 3
    • 79955432735 scopus 로고    scopus 로고
    • Advances in the discovery and development of heat-shock protein 90 inhibitors for cancer treatment
    • Patel HJ, Modi S, Chiosis G, et al. Advances in the discovery and development of heat-shock protein 90 inhibitors for cancer treatment. Expert Opin Drug Discov 2011;6(5):559-87
    • (2011) Expert Opin Drug Discov , vol.6 , Issue.5 , pp. 559-587
    • Patel, H.J.1    Modi, S.2    Chiosis, G.3
  • 4
    • 25844519550 scopus 로고    scopus 로고
    • HSP90 and the chaperoning of cancer
    • Whitesell L, Lindquist SL. HSP90 and the chaperoning of cancer. Nat Rev Cancer 2005;5(10):761-72
    • (2005) Nat Rev Cancer , vol.5 , Issue.10 , pp. 761-76772
    • Whitesell, L.1    Lindquist, S.L.2
  • 5
    • 0033502429 scopus 로고    scopus 로고
    • Geldanamycin as a potential anti-cancer agent: Its molecular target and biochemical activity
    • Neckers L, Schulte TW, Mimnaugh E. Geldanamycin as a potential anti-cancer agent: Its molecular target and biochemical activity. Invest New Drugs 1999;17(4):361-73
    • (1999) Invest New Drugs , vol.17 , Issue.4 , pp. 361-373
    • Neckers, L.1    Schulte, T.W.2    Mimnaugh, E.3
  • 6
    • 0032554763 scopus 로고    scopus 로고
    • Targeting of the protein chaperone, HSP90, by the transformation suppressing agent, radicicol
    • Sharma SV, Agatsuma T, Nakano H. Targeting of the protein chaperone, HSP90, by the transformation suppressing agent, radicicol. Oncogene 1998;16(20):2639-45
    • (1998) Oncogene , vol.16 , Issue.20 , pp. 2639-2645
    • Sharma, S.V.1    Agatsuma, T.2    Nakano, H.3
  • 7
    • 0031875042 scopus 로고    scopus 로고
    • The benzoquinone ansamycin 17-Allylamino-17-demethoxy geldanamycin binds to HSP90 and shares important biologic activities with geldanamycin
    • Schulte TW, Neckers LM. The benzoquinone ansamycin 17-Allylamino-17- demethoxy geldanamycin binds to HSP90 and shares important biologic activities with geldanamycin. Cancer Chemother Pharmacol 1998;42(4):273-9
    • (1998) Cancer Chemother Pharmacol , vol.42 , Issue.4 , pp. 273-279
    • Schulte, T.W.1    Neckers, L.M.2
  • 8
    • 23044441106 scopus 로고    scopus 로고
    • Phase i pharmacokinetic and pharmacodynamic study of 17-Allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies
    • Banerji U, O'Donnell A, Scurr M, et al. Phase I pharmacokinetic and pharmacodynamic study of 17-Allylamino, 17-demethoxygeldanamycin in patients with advanced malignancies. J Clin Oncol 2005;23(18):4152-61
    • (2005) J Clin Oncol , vol.23 , Issue.18 , pp. 4152-4161
    • Banerji, U.1    O'Donnell, A.2    Scurr, M.3
  • 9
    • 20044384168 scopus 로고    scopus 로고
    • Phase i trial of 17-Allylamino-17-demethoxygeldanamycin in patients with advanced cancer
    • Goetz MP, Toft D, Reid J, et al. Phase I trial of 17-Allylamino-17- demethoxygeldanamycin in patients with advanced cancer. J Clin Oncol 2005;23(6):1078-87
    • (2005) J Clin Oncol , vol.23 , Issue.6 , pp. 1078-1087
    • Goetz, M.P.1    Toft, D.2    Reid, J.3
  • 10
    • 20144375312 scopus 로고    scopus 로고
    • Phase i and pharmacologic study of 17-(allylamino)-17- demethoxygeldanamycin in adult patients with solid tumors
    • Grem JL, Morrison G, Guo XD, et al. Phase I and pharmacologic study of 17-(allylamino)-17-demethoxygeldanamycin in adult patients with solid tumors. J Clin Oncol 2005;23(9):1885-93
    • (2005) J Clin Oncol , vol.23 , Issue.9 , pp. 1885-1893
    • Grem, J.L.1    Morrison, G.2    Guo, X.D.3
  • 11
    • 84857039457 scopus 로고    scopus 로고
    • Advances in the clinical development of heat shock protein 90 (hsp90) inhibitors in cancers
    • Jhaveri K, Taldone T, Modi S, et al. Advances in the clinical development of heat shock protein 90 (Hsp90) inhibitors in cancers. Biochim Biophys Acta 2012;1823(3):742-55
    • (2012) Biochim Biophys Acta , vol.1823 , Issue.3 , pp. 742-755
    • Jhaveri, K.1    Taldone, T.2    Modi, S.3
  • 12
    • 59449108495 scopus 로고    scopus 로고
    • A phase II trial of 17-Allylamino-17-demethoxy geldanamycin in patients with hormonerefractory metastatic prostate cancer
    • Heath EI, Hillman DW, Vaishampayan U, et al. A phase II trial of 17-Allylamino-17-demethoxy geldanamycin in patients with hormonerefractory metastatic prostate cancer. Clin Cancer Res 2008;14(23):7940-6
    • (2008) Clin Cancer Res , vol.14 , Issue.23 , pp. 7940-7946
    • Heath, E.I.1    Hillman, D.W.2    Vaishampayan, U.3
  • 13
    • 58149340657 scopus 로고    scopus 로고
    • Phase II trial of 17-Allylamino-17-demethoxygeldanamycin in patients with metastatic melanoma
    • Solit DB, Osman I, Polsky D, et al. Phase II trial of 17-Allylamino-17-demethoxygeldanamycin in patients with metastatic melanoma. Clin Cancer Res 2008;14(24):8302-7
    • (2008) Clin Cancer Res , vol.14 , Issue.24 , pp. 8302-8307
    • Solit, D.B.1    Osman, I.2    Polsky, D.3
  • 14
    • 33747691089 scopus 로고    scopus 로고
    • A phase II trial of 17-(Allylamino)-17-demethoxy geldanamycin in patients with papillary and clear cell renal cell carcinoma
    • Ronnen EA, Kondagunta GV, Ishill N, et al. A phase II trial of 17-(Allylamino)-17-demethoxy geldanamycin in patients with papillary and clear cell renal cell carcinoma. Invest New Drugs 2006;24(6):543-6
    • (2006) Invest New Drugs , vol.24 , Issue.6 , pp. 543-546
    • Ronnen, E.A.1    Kondagunta, G.V.2    Ishill, N.3
  • 15
    • 84856554767 scopus 로고    scopus 로고
    • A phase ii trial of 17-Allylamino 17-demethoxygeldanamycin (17-Aag tanespimycin) in patients with metastatic melanoma
    • Pacey S, Gore M, Chao D, et al. A Phase II trial of 17-Allylamino, 17-demethoxygeldanamycin (17-AAG, tanespimycin) in patients with metastatic melanoma. Invest New Drugs 2012;30(1):341-9
    • (2012) Invest New Drugs , vol.30 , Issue.1 , pp. 341-349
    • Pacey, S.1    Gore, M.2    Chao, D.3
  • 16
    • 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, 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(15):5132-9
    • (2011) Clin Cancer Res , vol.17 , Issue.15 , pp. 5132-5139
    • Modi, S.1    Stopeck, A.2    Linden, H.3
  • 17
    • 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, 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(6):729-40
    • (2011) Br J Haematol , vol.153 , Issue.6 , pp. 729-740
    • Richardson, P.G.1    Chanan-Khan, A.A.2    Lonial, S.3
  • 18
    • 85067779728 scopus 로고    scopus 로고
    • PressRelease. Available from Last Accessed 8 January 2014]
    • PressRelease. Bristol-Myers Squibb Halts Development of Tanespimycin. 2008. Available from: Http://www. myelomabeacon.com/news/2010/07/22/ tanespimycin-development-halted/[Last Accessed 8 January 2014]
    • (2008) Bristol-Myers Squibb Halts Development of Tanespimycin.
  • 19
    • 84855457952 scopus 로고    scopus 로고
    • Hsp90 molecular chaperone inhibitors: Are we there yet?
    • Neckers L, Workman P. Hsp90 molecular chaperone inhibitors: Are we there yet? Clin Cancer Res 2012;18(1):64-76
    • (2012) Clin Cancer Res , vol.18 , Issue.1 , pp. 64-76
    • Neckers, L.1    Workman, P.2
  • 20
    • 4544337503 scopus 로고    scopus 로고
    • Synthesis and biological activities of novel 17-Aminogeldanamycin derivatives
    • Tian ZQ, Liu Y, Zhang D, et al. Synthesis and biological activities of novel 17-Aminogeldanamycin derivatives. Bioorg Med Chem 2004;12(20):5317-29
    • (2004) Bioorg Med Chem , vol.12 , Issue.20 , pp. 5317-5329
    • Tian, Z.Q.1    Liu, Y.2    Zhang, D.3
  • 21
    • 21244462689 scopus 로고    scopus 로고
    • In vivo antitumor efficacy of 17-DMAG (17-dimethylaminoethylamino-17- demethoxygeldanamycin hydrochloride), a water-soluble geldanamycin derivative
    • Hollingshead M, Alley M, Burger AM, et al. In vivo antitumor efficacy of 17-DMAG (17-dimethylaminoethylamino-17-demethoxygeldanamycin hydrochloride), a water-soluble geldanamycin derivative. Cancer Chemother Pharmacol 2005;56(2):115-25
    • (2005) Cancer Chemother Pharmacol , vol.56 , Issue.2 , pp. 115-125
    • Hollingshead, M.1    Alley, M.2    Burger, A.M.3
  • 22
    • 72449185268 scopus 로고    scopus 로고
    • Phase i trial of 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG), a heat shock protein inhibitor, administered twice weekly in patients with advanced malignancies
    • Kummar S, Gutierrez ME, Gardner ER, et al. Phase I trial of 17-dimethylaminoethylamino-17-demethoxygeldanamycin (17-DMAG), a heat shock protein inhibitor, administered twice weekly in patients with advanced malignancies. Eur J Cancer 2010;46(2):340-7
    • (2010) Eur J Cancer , vol.46 , Issue.2 , pp. 340-347
    • Kummar, S.1    Gutierrez, M.E.2    Gardner, E.R.3
  • 23
    • 77950929054 scopus 로고    scopus 로고
    • Phase i study of the heat shock protein 90 inhibitor alvespimycin (kos-1022 17-dmag) administered intravenously twice weekly to patients with acute myeloid leukemia
    • Lancet JE, Gojo I, Burton M, et al. Phase I study of the heat shock protein 90 inhibitor alvespimycin (KOS-1022, 17-DMAG) administered intravenously twice weekly to patients with acute myeloid leukemia. Leukemia 2010;24(4):699-705
    • (2010) Leukemia , vol.24 , Issue.4 , pp. 699-705
    • Lancet, J.E.1    Gojo, I.2    Burton, M.3
  • 24
    • 79952734485 scopus 로고    scopus 로고
    • A phase i study of the heat shock protein 90 inhibitor alvespimycin (17-dmag) given intravenously to patients with advanced solid tumors
    • Pacey S, Wilson RH, Walton M, et al. A phase I study of the heat shock protein 90 inhibitor alvespimycin (17-DMAG) given intravenously to patients with advanced solid tumors. Clin Cancer Res 2011;17(6):1561-70
    • (2011) Clin Cancer Res , vol.17 , Issue.6 , pp. 1561-1570
    • Pacey, S.1    Wilson, R.H.2    Walton, M.3
  • 25
    • 84866375177 scopus 로고    scopus 로고
    • A phase i dose-escalation trial of trastuzumab and alvespimycin hydrochloride (kos-1022; 17 dmag) in the treatment of advanced solid tumors
    • Jhaveri K, Miller K, Rosen L, et al. A phase I dose-escalation trial of trastuzumab and alvespimycin hydrochloride (KOS-1022; 17 DMAG) in the treatment of advanced solid tumors. Clin Cancer Res 2012;18(18):5090-8
    • (2012) Clin Cancer Res , vol.18 , Issue.18 , pp. 5090-5098
    • Jhaveri, K.1    Miller, K.2    Rosen, L.3
  • 26
    • 33751258297 scopus 로고    scopus 로고
    • Development of 17-Allylamino-17-demethoxygeldanamycin hydroquinone hydrochloride (IPI-504), an anti-cancer agent directed against Hsp90
    • Sydor JR, Normant E, Pien CS, et al. Development of 17-Allylamino-17- demethoxygeldanamycin hydroquinone hydrochloride (IPI-504), an anti-cancer agent directed against Hsp90. Proc Natl Acad Sci USA 2006;103(46):17408-13
    • (2006) Proc Natl Acad Sci USA , vol.103 , Issue.46 , pp. 17408-17413
    • Sydor, J.R.1    Normant, E.2    Pien, C.S.3
  • 27
    • 82255196140 scopus 로고    scopus 로고
    • A phase 1 study of ipi-504 (retaspimycin hydrochloride) in patients with relapsed or relapsed and refractory multiple myeloma
    • Siegel D, Jagannath S, Vesole DH, et al. A phase 1 study of IPI-504 (retaspimycin hydrochloride) in patients with relapsed or relapsed and refractory multiple myeloma. Leuk Lymphoma 2011;52(12):2308-15
    • (2011) Leuk Lymphoma , vol.52 , Issue.12 , pp. 2308-2315
    • Siegel, D.1    Jagannath, S.2    Vesole, D.H.3
  • 28
    • 80052330412 scopus 로고    scopus 로고
    • Multicenter phase ii trial of the heat shock protein 90 inhibitor retaspimycin hydrochloride (ipi-504) in patients with castration-resistant prostate cancer
    • Oh WK, Galsky MD, Stadler WM, et al. Multicenter phase II trial of the heat shock protein 90 inhibitor, retaspimycin hydrochloride (IPI-504), in patients with castration-resistant prostate cancer. Urology 2011;78(3):626-30
    • (2011) Urology , vol.78 , Issue.3 , pp. 626-630
    • Oh, W.K.1    Galsky, M.D.2    Stadler, W.M.3
  • 29
    • 79951885125 scopus 로고    scopus 로고
    • Activity of IPI-504, a novel heat-shock protein 90 inhibitor, in patients with molecularly defined non-small-cell lung cancer
    • Sequist LV, Gettinger S, Senzer NN, et al. Activity of IPI-504, a novel heat-shock protein 90 inhibitor, in patients with molecularly defined non-small-cell lung cancer. J Clin Oncol 2010;28(33):4953-60
    • (2010) J Clin Oncol , vol.28 , Issue.33 , pp. 4953-4960
    • Sequist, L.V.1    Gettinger, S.2    Senzer, N.N.3
  • 30
    • 51449118446 scopus 로고    scopus 로고
    • Inhibition of heat shock protein 90 (Hsp90) with the novel agent IPI-504 in metastatic GIST following failure of tyrosine kinase inhibitors (TKIs) or other sarcomas: Clinical results from phase i trial
    • abstract 10503
    • Wagner AJ, Morgan JA, Chugh R, et al. Inhibition of heat shock protein 90 (Hsp90) with the novel agent IPI-504 in metastatic GIST following failure of tyrosine kinase inhibitors (TKIs) or other sarcomas: Clinical results from phase I trial. J Clin Oncol 2008;26:abstract 10503
    • (2008) J Clin Oncol , vol.26
    • Wagner, A.J.1    Morgan, J.A.2    Chugh, R.3
  • 31
    • 79957896979 scopus 로고    scopus 로고
    • The hsp90 inhibitor ipi-504 rapidly lowers eml4-Alk levels and induces tumor regression in alk-driven nsclc models
    • Normant E, Paez G, West KA, et al. The Hsp90 inhibitor IPI-504 rapidly lowers EML4-ALK levels and induces tumor regression in ALK-driven NSCLC models. Oncogene 2011;30(22):2581-6
    • (2011) Oncogene , vol.30 , Issue.22 , pp. 2581-2586
    • Normant, E.1    Paez, G.2    West, K.A.3
  • 32
    • 78650363352 scopus 로고    scopus 로고
    • Association between anaplastic lymphoma kinase rearrangements (rALK) and the clinical activity of IPI-504 (retaspimycin hydrochloride), a novel Hsp90 inhibitor, in patients with nonsmall cell lung cancer (NSCLC)
    • abstract 7517
    • Sequist LV, Natale RB, Senzer NN, et al. Association between anaplastic lymphoma kinase rearrangements (rALK) and the clinical activity of IPI-504 (retaspimycin hydrochloride), a novel Hsp90 inhibitor, in patients with nonsmall cell lung cancer (NSCLC). J Clin Oncol 2010;28:abstract 7517
    • (2010) J Clin Oncol , vol.28
    • Sequist, L.V.1    Natale, R.B.2    Senzer, N.N.3
  • 33
    • 77954214309 scopus 로고    scopus 로고
    • Final results from a phase III study of IPI-504 (retaspimycin hydrochloride) versus placebo in patients (pts) with gastrointestinal stromal tumors (GIST) following failure of kinase inhibitor therapies
    • abstract-64
    • Demetri G, Le Cesne A, Von Mehren M, et al. Final results from a phase III study of IPI-504 (retaspimycin hydrochloride) versus placebo in patients (pts) with gastrointestinal stromal tumors (GIST) following failure of kinase inhibitor therapies. Gastrointestinal Cancers Symposium 2010;28:abstract-64
    • (2010) Gastrointestinal Cancers Symposium , vol.28
    • Demetri, G.1    Le Cesne, A.2    Von Mehren, M.3
  • 34
    • 84877581534 scopus 로고    scopus 로고
    • A multicenter trial evaluating retaspimycin hcl (ipi-504) plus trastuzumab in patients with advanced or metastatic her2-positive breast cancer
    • Modi S, Saura C, Henderson C, et al. A multicenter trial evaluating retaspimycin HCL (IPI-504) plus trastuzumab in patients with advanced or metastatic HER2-positive breast cancer. Breast Cancer Res Treat 2013;139(1):107-13
    • (2013) Breast Cancer Res Treat , vol.139 , Issue.1 , pp. 107-113
    • Modi, S.1    Saura, C.2    Henderson, C.3
  • 35
    • 1642503079 scopus 로고    scopus 로고
    • High-Throughput screening assay for inhibitors of heat-shock protein 90 ATPase activity
    • Rowlands MG, Newbatt YM, Prodromou C, et al. High-Throughput screening assay for inhibitors of heat-shock protein 90 ATPase activity. Anal Biochem 2004;327(2):176-83
    • (2004) Anal Biochem , vol.327 , Issue.2 , pp. 176-183
    • Rowlands, M.G.1    Newbatt, Y.M.2    Prodromou, C.3
  • 36
    • 20644448390 scopus 로고    scopus 로고
    • The identification syn thesis, protein crystal structure and in vitro biochemical evaluation of a new 3,4-diarylpyrazole class of Hsp90 inhibitors
    • Cheung KM, Matthews TP, James K, et al. The identification, synthesis, protein crystal structure and in vitro biochemical evaluation of a new 3,4-diarylpyrazole class of Hsp90 inhibitors. Bioorg Med Chem Lett 2005;15(14):3338-43
    • (2005) Bioorg Med Chem Lett , vol.15 , Issue.14 , pp. 3338-3343
    • Cheung, K.M.1    Matthews, T.P.2    James, K.3
  • 37
    • 48949119477 scopus 로고    scopus 로고
    • NVP-AUY922: A small molecule HSP90 inhibitor with potent antitumor activity in preclinical breast cancer models
    • Jensen MR, Schoepfer J, Radimerski T, et al. NVP-AUY922: A small molecule HSP90 inhibitor with potent antitumor activity in preclinical breast cancer models. Breast Cancer Res 2008;10(2):R33
    • (2008) Breast Cancer Res , vol.10 , Issue.2
    • Jensen, M.R.1    Schoepfer, J.2    Radimerski, T.3
  • 38
    • 79960983822 scopus 로고    scopus 로고
    • AUY922, a novel HSP90 inhibitor: Final results of a first-in-human study in patients with advanced solid malignancies
    • Suppl):abstract 2528
    • Samuel TA, Sessa C, Britten C, et al. AUY922, a novel HSP90 inhibitor: Final results of a first-in-human study in patients with advanced solid malignancies. J Clin Oncol 2010;28(Suppl):abstract 2528
    • (2010) J Clin Oncol , vol.28
    • Samuel, T.A.1    Sessa, C.2    Britten, C.3
  • 39
    • 84857036694 scopus 로고    scopus 로고
    • Use of biomarkers and imaging to evaluate the treatment effect of AUY922, an Hsp90 inhibitor, in patients with HER2+ or ER+ metastatic breast cancer
    • Suppl):abstract e11024
    • Schroder C, Pederson JV, Chua S, et al. Use of biomarkers and imaging to evaluate the treatment effect of AUY922, an Hsp90 inhibitor, in patients with HER2+ or ER+ metastatic breast cancer. J Clin Oncol 2011;29(Suppl):abstract e11024
    • (2011) J Clin Oncol , vol.29
    • Schroder, C.1    Pederson, J.V.2    Chua, S.3
  • 40
    • 84866382273 scopus 로고    scopus 로고
    • Phase II study of the HSP90 inhibitor AUY922 in patients with previously treated, advanced non-small cell lung cancer (NSCLC)
    • Suppl):abstract 7543
    • Garon EB, Moran T, Barlesi F, et al. Phase II study of the HSP90 inhibitor AUY922 in patients with previously treated, advanced non-small cell lung cancer (NSCLC). J Clin Oncol 2012;30(Suppl):abstract 7543
    • (2012) J Clin Oncol , vol.30
    • Garon, E.B.1    Moran, T.2    Barlesi, F.3
  • 41
    • 84894082325 scopus 로고    scopus 로고
    • A phase II study of HSP90 inhibitor AUY922 and erlotinib (E) for patients (pts) with EGFR-mutant lung cancer and acquired resistance (AR) to EGFR tyrosine kinase inhibitors (EGFR TKIs)
    • abstract 8036
    • Johnson ML, Hart EM, Rademaker A, et al. A phase II study of HSP90 inhibitor AUY922 and erlotinib (E) for patients (pts) with EGFR-mutant lung cancer and acquired resistance (AR) to EGFR tyrosine kinase inhibitors (EGFR TKIs). J Clin Oncol 2013;31:abstract 8036
    • (2013) J Clin Oncol , vol.31
    • Johnson, M.L.1    Hart, E.M.2    Rademaker, A.3
  • 42
    • 84875533868 scopus 로고    scopus 로고
    • Phase IB/II study of the HSP90 inhibitor AUY922, in combination with trastuzumab, in patients with HER2 positive advanced breast cancer
    • Suppl):abstract 530
    • Kong A, Rea D, Ahmed S, et al. Phase IB/II study of the HSP90 inhibitor AUY922, in combination with trastuzumab, in patients with HER2 positive advanced breast cancer. J Clin Oncol 2012;30(Suppl):abstract 530
    • (2012) J Clin Oncol , vol.30
    • Kong, A.1    Rea, D.2    Ahmed, S.3
  • 43
    • 77955863827 scopus 로고    scopus 로고
    • Fragment-based drug discovery applied to Hsp90. Discovery of two lead series with high ligand efficiency
    • Murray CW, Carr MG, Callaghan O, et al. Fragment-based drug discovery applied to Hsp90. Discovery of two lead series with high ligand efficiency. J Med Chem 2010;53(16):5942-55
    • (2010) J Med Chem , vol.53 , Issue.16 , pp. 5942-5955
    • Murray, C.W.1    Carr, M.G.2    Callaghan, O.3
  • 44
    • 77955873344 scopus 로고    scopus 로고
    • Discovery of (2,4-dihydroxy-5-isopropylphenyl)-[5-(4-methylpiperazin-1- ylmethyl)-1,3-dihydroisoindol-2-yl] methanone (AT13387), a novel inhibitor of the molecular chaperone Hsp90 by fragment based drug design
    • Woodhead AJ, Angove H, Carr MG, et al. Discovery of (2,4-dihydroxy-5- isopropylphenyl)-[5-(4-methylpiperazin-1-ylmethyl)-1,3-dihydroisoindol-2-yl] methanone (AT13387), a novel inhibitor of the molecular chaperone Hsp90 by fragment based drug design. J Med Chem 2010;53(16):5956-69
    • (2010) J Med Chem , vol.53 , Issue.16 , pp. 5956-5969
    • Woodhead, A.J.1    Angove, H.2    Carr, M.G.3
  • 45
    • 84866414054 scopus 로고    scopus 로고
    • First-in-human phase i study: Results of a second-generation non-Ansamycin heat shock protein 90 (HSP90) inhibitor AT13387 in refractory solid tumors
    • Suppl):abstract 3028
    • Mahadevan D, Rensvold DM, Kurtin SE, et al. First-in-human phase I study: Results of a second-generation non-Ansamycin heat shock protein 90 (HSP90) inhibitor AT13387 in refractory solid tumors. J Clin Oncol 2012;30(Suppl): abstract 3028
    • (2012) J Clin Oncol , vol.30
    • Mahadevan, D.1    Rensvold, D.M.2    Kurtin, S.E.3
  • 46
    • 84875811506 scopus 로고    scopus 로고
    • Phase l study assessing a two-consecutive-day (QD x 2) dosing schedule of the HSP90 inhibitor, AT13387, in patients with advanced solid tumors
    • abstract 3087
    • Do KT, Speranza G, Chen AP, et al. Phase l study assessing a two-consecutive-day (QD x 2) dosing schedule of the HSP90 inhibitor, AT13387, in patients with advanced solid tumors. J Clin Oncol 2012;30:abstract 3087
    • (2012) J Clin Oncol , vol.30
    • Do, K.T.1    Speranza, G.2    Chen, A.P.3
  • 47
    • 84856832510 scopus 로고    scopus 로고
    • Ganetespib a unique triazolone-containing hsp90 inhibitor exhibits potent antitumor activity and a superior safety profile for cancer therapy
    • Ying W, Du Z, Sun L, et al. Ganetespib, a unique triazolone-containing Hsp90 inhibitor, exhibits potent antitumor activity and a superior safety profile for cancer therapy. Mol Cancer Ther 2012;11(2):475-84
    • (2012) Mol Cancer Ther , vol.11 , Issue.2 , pp. 475-484
    • Ying, W.1    Du, Z.2    Sun, L.3
  • 48
    • 84874446994 scopus 로고    scopus 로고
    • Recent updates on the development of ganetespib as a Hsp90 inhibitor
    • Choi HK, Lee K. Recent updates on the development of ganetespib as a Hsp90 inhibitor. Arch Pharm Res 2012;35(11):1855-9
    • (2012) Arch Pharm Res , vol.35 , Issue.11 , pp. 1855-1859
    • Choi, H.K.1    Lee, K.2
  • 49
    • 84875316604 scopus 로고    scopus 로고
    • A first in human, safety, pharmacokinetics, and clinical activity phase i study of once weekly administration of the Hsp90 inhibitor ganetespib (STA-9090) in patients with solid malignancies
    • Goldman JW, Raju RN, Gordon GA, et al. A first in human, safety, pharmacokinetics, and clinical activity phase I study of once weekly administration of the Hsp90 inhibitor ganetespib (STA-9090) in patients with solid malignancies. BMC Cancer 2013;13:152
    • (2013) BMC Cancer , vol.13 , pp. 152
    • Goldman, J.W.1    Raju, R.N.2    Gordon, G.A.3
  • 50
    • 84857042166 scopus 로고    scopus 로고
    • A phase i dose escalation study of the Hsp90 inhibitor ganetespib (STA-9090) administered twice weekly in patients with solid tumors: Updated report
    • abstract 3051
    • Cho D, Heath EI, Cleary JM, et al. A phase I dose escalation study of the Hsp90 inhibitor ganetespib (STA-9090) administered twice weekly in patients with solid tumors: Updated report. J Clin Oncol 2011;29:abstract 3051
    • (2011) J Clin Oncol , vol.29
    • Cho, D.1    Heath, E.I.2    Cleary, J.M.3
  • 51
    • 85006484740 scopus 로고    scopus 로고
    • A phase 1/2 study of the potent Hsp90 inhibitor STA-9090 administered once weekly in subjects with hematologic malignancies
    • abstract 3294
    • Lancet JE, Smith BD, Bradley R, et al. A phase 1/2 study of the potent Hsp90 inhibitor STA-9090 administered once weekly in subjects with hematologic malignancies. Blood 2010;abstract 3294
    • (2010) Blood
    • Lancet, J.E.1    Smith, B.D.2    Bradley, R.3
  • 52
    • 84857060831 scopus 로고    scopus 로고
    • A phase i study of the potent Hsp90 Inhibitor STA-9090 administered twice weekly in subjects with hematologic malignancies
    • abstract 2898
    • Padmanabhan S, Kelly K, Heaney M, et al. A phase I study of the potent Hsp90 Inhibitor STA-9090 administered twice weekly in subjects with hematologic malignancies. Blood 2010;116:abstract 2898
    • (2010) Blood , vol.116
    • Padmanabhan, S.1    Kelly, K.2    Heaney, M.3
  • 53
    • 84878971581 scopus 로고    scopus 로고
    • A multicenter phase ii study of ganetespib monotherapy in patients with genotypically defined advanced non-small cell lung cancer
    • Socinski MA, Goldman J, El-Hariry I, et al. A multicenter phase II study of ganetespib monotherapy in patients with genotypically defined advanced non-small cell lung cancer. Clin Cancer Res 2013;19(11):3068-77
    • (2013) Clin Cancer Res , vol.19 , Issue.11 , pp. 3068-3077
    • Socinski, M.A.1    Goldman, J.2    El-Hariry, I.3
  • 54
    • 84898431762 scopus 로고    scopus 로고
    • A phase II open-label study of ganetespib, a novel heat shock protein 90 inhibitor for patients with metastatic breast cancer
    • Epub ahead of print
    • Jhaveri K, Chandarlapaty S, Lake D, et al. A phase II open-label study of ganetespib, a novel heat shock protein 90 inhibitor for patients with metastatic breast cancer. Clin Breast Cancer 2013; Epub ahead of print
    • (2013) Clin Breast Cancer
    • Jhaveri, K.1    Chandarlapaty, S.2    Lake, D.3
  • 55
    • 84857055228 scopus 로고    scopus 로고
    • An open-label phase II study of the Hsp90 inhibitor ganetespib (STA-9090) in patients (pts) with metastatic and/or unresectable GIST
    • Suppl):abstract 10011
    • Demetri G, Heinrich MC, Chmielowski B, et al. An open-label phase II study of the Hsp90 inhibitor ganetespib (STA-9090) in patients (pts) with metastatic and/or unresectable GIST. J Clin Oncol 2011;29(Suppl):abstract 10011
    • (2011) J Clin Oncol , vol.29
    • Demetri, G.1    Heinrich, M.C.2    Chmielowski, B.3
  • 56
    • 0038404927 scopus 로고    scopus 로고
    • Inhibition of heat shock protein 90 function down-regulates Akt kinase and sensitizes tumors to Taxol
    • Solit DB, Basso AD, Olshen AB, et al. Inhibition of heat shock protein 90 function down-regulates Akt kinase and sensitizes tumors to Taxol. Cancer Res 2003;63(9):2139-44
    • (2003) Cancer Res , vol.63 , Issue.9 , pp. 2139-2144
    • Solit, D.B.1    Basso, A.D.2    Olshen, A.B.3
  • 57
    • 84865839031 scopus 로고    scopus 로고
    • Hsp90 inhibitors for cancer therapy and overcoming drug resistance
    • Jhaveri K, Modi S. Hsp90 inhibitors for cancer therapy and overcoming drug resistance. Adv Pharmacol 2012;65:471-517
    • (2012) Adv Pharmacol , vol.65 , pp. 471-517
    • Jhaveri, K.1    Modi, S.2
  • 58
    • 84887029257 scopus 로고    scopus 로고
    • A randomized study of ganetespib, a heat shock protein 90 inhibitor, in combination with docetaxel versus docetaxel alone for second-line therapy of lung adenocarcinoma (GALAXY-1)
    • Suppl):abstract CRA8007
    • Ramalingam S, Goss GD, Andric ZG, et al. A randomized study of ganetespib, a heat shock protein 90 inhibitor, in combination with docetaxel versus docetaxel alone for second-line therapy of lung adenocarcinoma (GALAXY-1). J Clin Oncol 2013;31(Suppl):abstract CRA8007
    • (2013) J Clin Oncol , vol.31
    • Ramalingam, S.1    Goss, G.D.2    Andric, Z.G.3
  • 59
    • 84892764962 scopus 로고    scopus 로고
    • Preclinical activity profile and therapeutic efficacy of the hsp90 inhibitor ganetespib in triple-negative breast cancer
    • Proia DA, Zhang C, Sequeira M, et al. Preclinical activity profile and therapeutic efficacy of the Hsp90 inhibitor ganetespib in triple-negative breast cancer. Clin Cancer Res 2013;20(2):413-24
    • (2013) Clin Cancer Res , vol.20 , Issue.2 , pp. 413-424
    • Proia, D.A.1    Zhang, C.2    Sequeira, M.3
  • 60
    • 79955619964 scopus 로고    scopus 로고
    • The safety, pharmacokinetics and pharmacodynamics of KW-2478, a novel Hsp90 antagonist, in patients with B-cell malignancies: A first-in-man, phase I, multicentre, open-label, dose escalation study
    • abstract 2777
    • Cavenagh JD, Yong K, Byrne J, et al. The safety, pharmacokinetics and pharmacodynamics of KW-2478, a novel Hsp90 antagonist, in patients with B-cell malignancies: A first-in-man, phase I, multicentre, open-label, dose escalation study. Myeloma-Therapy Blood 2008;112:abstract 2777
    • (2008) Myeloma-Therapy Blood , vol.112
    • Cavenagh, J.D.1    Yong, K.2    Byrne, J.3
  • 61
    • 85067781314 scopus 로고    scopus 로고
    • A phase 1/2 study of KW-2478, an Hsp 90 inhibitor, in combination with bortezomib (BTZ) in patients (Pts) with relapsed/refractory (R/R) multiple myeloma (MM)
    • abstract 1967
    • Cavenagh J, Baylon HG, Caguioa PB, et al. A phase 1/2 study of KW-2478, an Hsp 90 inhibitor, in combination with bortezomib (BTZ) in patients (Pts) with relapsed/refractory (R/R) multiple myeloma (MM). Myeloma: Therapy, excluding Transplantation: Poster I Blood 2013;122:abstract 1967
    • (2013) Myeloma: Therapy, Excluding Transplantation: Poster i Blood , vol.122
    • Cavenagh, J.1    Baylon, H.G.2    Caguioa, P.B.3
  • 62
    • 74249105371 scopus 로고    scopus 로고
    • Purine-scaffold Hsp90 inhibitors
    • Taldone T, Chiosis G. Purine-scaffold Hsp90 inhibitors. Curr Top Med Chem 2009;9(15):1436-46
    • (2009) Curr Top Med Chem , vol.9 , Issue.15 , pp. 1436-1446
    • Taldone, T.1    Chiosis, G.2
  • 63
    • 0036718795 scopus 로고    scopus 로고
    • ATPases as drug targets: Learning from their structure
    • Chene P. ATPases as drug targets: Learning from their structure. Nat Rev Drug Discov 2002;1(9):665-73
    • (2002) Nat Rev Drug Discov , vol.1 , Issue.9 , pp. 665-673
    • Chene, P.1
  • 64
    • 0035071607 scopus 로고    scopus 로고
    • A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes Her2 degradation and the growth arrest and differentiation of breast cancer cells
    • Chiosis G, Timaul MN, Lucas B, et al. A small molecule designed to bind to the adenine nucleotide pocket of Hsp90 causes Her2 degradation and the growth arrest and differentiation of breast cancer cells. Chem Biol 2001;8(3):289-99
    • (2001) Chem Biol , vol.8 , Issue.3 , pp. 289-299
    • Chiosis, G.1    Timaul, M.N.2    Lucas, B.3
  • 65
    • 34250877881 scopus 로고    scopus 로고
    • Rationally designed high-Affinity 2-Amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity
    • Kasibhatla SR, Hong K, Biamonte MA, et al. Rationally designed high-Affinity 2-Amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity. J Med Chem 2007;50(12):2767-78
    • (2007) J Med Chem , vol.50 , Issue.12 , pp. 2767-2778
    • Kasibhatla, S.R.1    Hong, K.2    Biamonte, M.A.3
  • 66
    • 84871563835 scopus 로고    scopus 로고
    • Phase ii study of the hsp90-inhibitor biib021 in gastrointestinal stromal tumors
    • Dickson MA, Okuno SH, Keohan ML, et al. Phase II study of the HSP90-inhibitor BIIB021 in gastrointestinal stromal tumors. Ann Oncol 2013;24(1):252-7
    • (2013) Ann Oncol , vol.24 , Issue.1 , pp. 252-257
    • Dickson, M.A.1    Okuno, S.H.2    Keohan, M.L.3
  • 67
    • 84857060835 scopus 로고    scopus 로고
    • Phase 1 dose-escalation study of the heat shock protein 90 inhibitor BIIB021 with trastuzumab in HER2+ metastatic breast cancer
    • abstract P3-14-02
    • Modi S, Ismail-Khan R, Munster P, et al. Phase 1 dose-escalation study of the heat shock protein 90 inhibitor BIIB021 with trastuzumab in HER2+ metastatic breast cancer. Cancer Res 2010;70(24 Suppl 2):abstract P3-14-02
    • (2010) Cancer Res , vol.70 , Issue.24 SUPPL. 2
    • Modi, S.1    Ismail-Khan, R.2    Munster, P.3
  • 68
    • 79955668058 scopus 로고    scopus 로고
    • Biogen idec restructures sharpens neurology focus
    • Mitchell P. Biogen Idec restructures, sharpens neurology focus. Nat Biotechnol 2011;29(1):7-8
    • (2011) Nat Biotechnol , vol.29 , Issue.1 , pp. 7-8
    • Mitchell, P.1
  • 69
    • 30444447639 scopus 로고    scopus 로고
    • Identification of potent water soluble purine-scaffold inhibitors of the heat shock protein 90
    • He H, Zatorska D, Kim J, et al. Identification of potent water soluble purine-scaffold inhibitors of the heat shock protein 90. J Med Chem 2006;49(1):381-90
    • (2006) J Med Chem , vol.49 , Issue.1 , pp. 381-390
    • He, H.1    Zatorska, D.2    Kim, J.3
  • 70
    • 84898482545 scopus 로고    scopus 로고
    • Progress in first-in-human trial of Hsp90-Targeted PET imaging in cancer patients
    • abstract 279
    • Dunphy M, Chiosis G, Beattie B, et al. Progress in first-in-human trial of Hsp90-Targeted PET imaging in cancer patients. J Nucl Med 2013;54(Suppl 2):abstract 279
    • (2013) J Nucl Med , vol.54 , Issue.SUPPL. 2
    • Dunphy, M.1    Chiosis, G.2    Beattie, B.3
  • 71
    • 84898409954 scopus 로고    scopus 로고
    • Using 124I-PU-H71 PET imaging to predict intratumoral concentration in patients on a phase i trial of PU-H71
    • Suppl):abstract 11076
    • Gerecitano JF, Modi S, Gajria D, et al. Using 124I-PU-H71 PET imaging to predict intratumoral concentration in patients on a phase I trial of PU-H71. J Clin Oncol 2013;31(Suppl):abstract 11076
    • (2013) J Clin Oncol , vol.31
    • Gerecitano, J.F.1    Modi, S.2    Gajria, D.3
  • 72
    • 84866342651 scopus 로고    scopus 로고
    • Discovery of (2S)-1-[4-(2-{6-Amino-8-[(6-bromo-1,3-benzodioxol-5-yl) sulfanyl]-9H-purin-9-yl}et hyl)piperidin-1-yl]-2-hydroxypropan-1-one (MPC-3100), a purine-based Hsp90 inhibitor
    • Kim SH, Bajji A, Tangallapally R, et al. Discovery of (2S)-1-[4-(2-{6-Amino-8-[(6-bromo-1,3-benzodioxol-5-yl)sulfanyl]-9H-purin-9-yl} et hyl)piperidin-1-yl]-2-hydroxypropan-1-one (MPC-3100), a purine-based Hsp90 inhibitor. J Med Chem 2012;55(17):7480-501
    • (2012) J Med Chem , vol.55 , Issue.17 , pp. 7480-7501
    • Kim, S.H.1    Bajji, A.2    Tangallapally, R.3
  • 74
    • 67449138839 scopus 로고    scopus 로고
    • CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacologic properties for cancer therapy
    • Bao R, Lai CJ, Qu H, et al. CUDC-305, a novel synthetic HSP90 inhibitor with unique pharmacologic properties for cancer therapy. Clin Cancer Res 2009;15(12):4046-57
    • (2009) Clin Cancer Res , vol.15 , Issue.12 , pp. 4046-4057
    • Bao, R.1    Lai, C.J.2    Qu, H.3
  • 75
    • 84884257315 scopus 로고    scopus 로고
    • Experimental and structural testing module to analyze paralogue-specificity and affinity in the Hsp90 inhibitors series
    • Taldone T, Patel PD, Patel M, et al. Experimental and structural testing module to analyze paralogue-specificity and affinity in the Hsp90 inhibitors series. J Med Chem 2013;56(17):6803-18
    • (2013) J Med Chem , vol.56 , Issue.17 , pp. 6803-6818
    • Taldone, T.1    Patel, P.D.2    Patel, M.3
  • 76
    • 84880799099 scopus 로고    scopus 로고
    • A phase i study of Debio 0932, an oral HSP90 inhibitor, in patients with solid tumors
    • abstract 3026
    • Isambert N, Hollebecque A, Berge Y, et al. A phase I study of Debio 0932, an oral HSP90 inhibitor, in patients with solid tumors. J Clin Oncol 2012;30:abstract 3026
    • (2012) J Clin Oncol , vol.30
    • Isambert, N.1    Hollebecque, A.2    Berge, Y.3
  • 77
    • 77955444211 scopus 로고    scopus 로고
    • Application of chemoproteomics to drug discovery: Identification of a clinical candidate targeting hsp90
    • Fadden P, Huang KH, Veal JM, et al. Application of chemoproteomics to drug discovery: Identification of a clinical candidate targeting Hsp90. Chem Biol 2010;17(7):686-94
    • (2010) Chem Biol , vol.17 , Issue.7 , pp. 686-694
    • Fadden, P.1    Huang, K.H.2    Veal, J.M.3
  • 78
    • 80455162319 scopus 로고    scopus 로고
    • A phase i study of pf-04929113 (snx-5422) an orally bioavailable heat shock protein 90 inhibitor in patients with refractory solid tumor malignancies and lymphomas
    • Rajan A, Kelly RJ, Trepel JB, et al. A phase I study of PF-04929113 (SNX-5422), an orally bioavailable heat shock protein 90 inhibitor, in patients with refractory solid tumor malignancies and lymphomas. Clin Cancer Res 2011;17(21):6831-9
    • (2011) Clin Cancer Res , vol.17 , Issue.21 , pp. 6831-6839
    • Rajan, A.1    Kelly, R.J.2    Trepel, J.B.3
  • 79
    • 85067782953 scopus 로고    scopus 로고
    • Esanex: Out of stealth mode (barely)
    • Available from
    • Esanex: Out of stealth mode (barely). HSP90 Inhibitors Central. 2013. Available from: Http://www. hsp90central.com/1/post/2013/01/esanexout-of- stealth-mode-barely.html [Last Accessed 8 January 2014]
    • (2013) HSP90 Inhibitors Central.
  • 80
    • 84859379802 scopus 로고    scopus 로고
    • The novel oral hsp90 inhibitor nvp-hsp990 exhibits potent and broad-spectrum antitumor activities in vitro and in vivo
    • Menezes DL, Taverna P, Jensen MR, et al. The novel oral Hsp90 inhibitor NVP-HSP990 exhibits potent and broad-spectrum antitumor activities in vitro and in vivo. Mol Cancer Ther 2012;11(3):730-9
    • (2012) Mol Cancer Ther , vol.11 , Issue.3 , pp. 730-739
    • Menezes, D.L.1    Taverna, P.2    Jensen, M.R.3
  • 81
    • 85067771237 scopus 로고    scopus 로고
    • Phase i dose-escalation, open-label study of HSP990 administered orally in adult patients with advanced solid malignancies
    • Mattos-Arruda LD, Siu LL, Cortes J, et al. Phase I dose-escalation, open-label study of HSP990 administered orally in adult patients with advanced solid malignancies. J Clin Oncol 2013;31(Suppl)
    • (2013) J Clin Oncol , vol.31 , Issue.SUPPL
    • Mattos-Arruda, L.D.1    Siu, L.L.2    Cortes, J.3
  • 82
    • 85067756836 scopus 로고    scopus 로고
    • Vernalis30 June 2012.2012. Available From Last Accessed 9 January 2014]
    • Vernalis. Interim results for the six months ended 30 June 2012.2012. Available from: Http://www. vernalis.com/media-centre/latest-releases/2012- releases/642-interim-results-for-Thesix-months-ended-30-june-2012 [Last Accessed 9 January 2014]
    • Interim Results for the Six Months Ended
  • 83
    • 84865142661 scopus 로고    scopus 로고
    • Discovery of xl888: A novel tropane-derived small molecule inhibitor of hsp90
    • Bussenius J, Blazey CM, Aay N, et al. Discovery of XL888: A novel tropane-derived small molecule inhibitor of HSP90. Bioorg Med Chem Lett 2012;22(17):5396-404
    • (2012) Bioorg Med Chem Lett , vol.22 , Issue.17 , pp. 5396-5404
    • Bussenius, J.1    Blazey, C.M.2    Aay, N.3
  • 84
    • 84860533156 scopus 로고    scopus 로고
    • The hsp90 inhibitor xl888 overcomes braf inhibitor resistance mediated through diverse mechanisms
    • Paraiso KH, Haarberg HE, Wood E, et al. The HSP90 inhibitor XL888 overcomes BRAF inhibitor resistance mediated through diverse mechanisms. Clin Cancer Res 2012;18(9):2502-14
    • (2012) Clin Cancer Res , vol.18 , Issue.9 , pp. 2502-2514
    • Paraiso, K.H.1    Haarberg, H.E.2    Wood, E.3
  • 85
    • 84857050136 scopus 로고    scopus 로고
    • HSP90 as a platform for the assembly of more effective cancer chemotherapy
    • Whitesell L, Lin NU. HSP90 as a platform for the assembly of more effective cancer chemotherapy. Biochim Biophys Acta 2012;1823(3):756-66
    • (2012) Biochim Biophys Acta , vol.1823 , Issue.3 , pp. 756-766
    • Whitesell, L.1    Lin, N.U.2
  • 86
    • 50349093362 scopus 로고    scopus 로고
    • A phase i study of 17-Allylamino-17-demethoxygeldanamycin combined with paclitaxel in patients with advanced solid malignancies
    • Ramalingam SS, Egorin MJ, Ramanathan RK, et al. A phase I study of 17-Allylamino-17-demethoxygeldanamycin combined with paclitaxel in patients with advanced solid malignancies. Clin Cancer Res 2008;14(11):3456-61
    • (2008) Clin Cancer Res , vol.14 , Issue.11 , pp. 3456-3461
    • Ramalingam, S.S.1    Egorin, M.J.2    Ramanathan, R.K.3
  • 87
    • 0042885973 scopus 로고    scopus 로고
    • The Hsp90 chaperone complex as a novel target for cancer therapy
    • Goetz MP, Toft DO, Ames MM, et al. The Hsp90 chaperone complex as a novel target for cancer therapy. Ann Oncol 2003;14(8):1169-76
    • (2003) Ann Oncol , vol.14 , Issue.8 , pp. 1169-1176
    • Goetz, M.P.1    Toft, D.O.2    Ames, M.M.3
  • 88
    • 11244337455 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of 17-demethoxy 17-[[(2-dimethylamino) ethyl] amino] geldanamycin (17DMAG, NSC 707545) in C.B-17 SCID mice bearing MDA-MB-231 human breast cancer xenografts
    • Eiseman JL, Lan J, Lagattuta TF, et al. Pharmacokinetics and pharmacodynamics of 17-demethoxy 17-[[(2-dimethylamino) ethyl] amino] geldanamycin (17DMAG, NSC 707545) in C.B-17 SCID mice bearing MDA-MB-231 human breast cancer xenografts. Cancer Chemother Pharmacol 2005;55(1):21-32
    • (2005) Cancer Chemother Pharmacol , vol.55 , Issue.1 , pp. 21-32
    • Eiseman, J.L.1    Lan, J.2    Lagattuta, T.F.3
  • 89
    • 3042553538 scopus 로고    scopus 로고
    • Targeting wide-range oncogenic transformation via PU24FCl, a specific inhibitor of tumor Hsp90
    • Vilenchik M, Solit D, Basso A, et al. Targeting wide-range oncogenic transformation via PU24FCl, a specific inhibitor of tumor Hsp90. Chem Biol 2004;11(6):787-97
    • (2004) Chem Biol , vol.11 , Issue.6 , pp. 787-797
    • Vilenchik, M.1    Solit, D.2    Basso, A.3
  • 90
    • 0141484615 scopus 로고    scopus 로고
    • A high-Affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors
    • Kamal A, Thao L, Sensintaffar J, et al. A high-Affinity conformation of Hsp90 confers tumour selectivity on Hsp90 inhibitors. Nature 2003;425(6956):407-10
    • (2003) Nature , vol.425 , Issue.6956 , pp. 407-410
    • Kamal, A.1    Thao, L.2    Sensintaffar, J.3
  • 91
    • 80054851888 scopus 로고    scopus 로고
    • Affinity-based proteomics reveal cancerspecific networks coordinated by hsp90
    • Moulick K, Ahn JH, Zong H, et al. Affinity-based proteomics reveal cancerspecific networks coordinated by Hsp90. Nat Chem Biol 2011;7(11):818-26
    • (2011) Nat Chem Biol , vol.7 , Issue.11 , pp. 818-826
    • Moulick, K.1    Ahn, J.H.2    Zong, H.3
  • 92
    • 34247499347 scopus 로고    scopus 로고
    • Evaluation of plasma insulin-like growth factor binding protein 2 and Her-2 extracellular domain as biomarkers for 17-Allylamino-17- demethoxygeldanamycin treatment of adult patients with advanced solid tumors
    • Eiseman JL, Guo J, Ramanathan RK, et al. Evaluation of plasma insulin-like growth factor binding protein 2 and Her-2 extracellular domain as biomarkers for 17-Allylamino-17-demethoxygeldanamycin treatment of adult patients with advanced solid tumors. Clin Cancer Res 2007;13(7):2121-7
    • (2007) Clin Cancer Res , vol.13 , Issue.7 , pp. 2121-2127
    • Eiseman, J.L.1    Guo, J.2    Ramanathan, R.K.3
  • 93
    • 37649018967 scopus 로고    scopus 로고
    • Inhibition of the heat shock protein 90 (Hsp90) chaperone with the novel agent IPI-504 to overcome resistance to tyrosine kinase inhibitors (TKIs) in metastatic GIST: Updated results of a phase i trial
    • abstract 10024
    • Demetri GD, George S, Morgan JA, et al. Inhibition of the heat shock protein 90 (Hsp90) chaperone with the novel agent IPI-504 to overcome resistance to tyrosine kinase inhibitors (TKIs) in metastatic GIST: Updated results of a phase I trial. J Clin Oncol 2007;25:abstract 10024
    • (2007) J Clin Oncol , vol.25
    • Demetri, G.D.1    George, S.2    Morgan, J.A.3
  • 94
    • 77749309983 scopus 로고    scopus 로고
    • Measuring the pharmacodynamic effects of a novel hsp90 inhibitor on her2neu expression in mice using zr-dfo-Trastuzumab
    • Holland JP, Caldas-Lopes E, Divilov V, et al. Measuring the pharmacodynamic effects of a novel Hsp90 inhibitor on HER2/neu expression in mice using Zr-DFO-Trastuzumab. PLoS ONE 2010;5(1):e8859
    • (2010) PLoS ONE , vol.5 , Issue.1
    • Holland, J.P.1    Caldas-Lopes, E.2    Divilov, V.3
  • 95
    • 77952302437 scopus 로고    scopus 로고
    • 89Zr-bevacizumab PET of early antiangiogenic tumor response to treatment with HSP90 inhibitor NVP-AUY922
    • Nagengast WB, de Korte MA, Oude Munnink TH, et al. 89Zr-bevacizumab PET of early antiangiogenic tumor response to treatment with HSP90 inhibitor NVP-AUY922. J Nucl Med 2010;51(5):761-7
    • (2010) J Nucl Med , vol.51 , Issue.5 , pp. 761-767
    • Nagengast, W.B.1    De Korte, M.A.2    Oude Munnink, T.H.3
  • 96
    • 75149113119 scopus 로고    scopus 로고
    • 89 Zr-Trastuzumab PET visualises HER2 downregulation by the HSP90 inhibitor NVP-AUY922 in a human tumour xenograft
    • Oude Munnink TH, Korte MA, Nagengast WB, et al (89)Zr-Trastuzumab PET visualises HER2 downregulation by the HSP90 inhibitor NVP-AUY922 in a human tumour xenograft. Eur J Cancer 2010;46(3):678-84
    • (2010) Eur J Cancer , vol.46 , Issue.3 , pp. 678-684
    • Oude Munnink, T.H.1    Korte, M.A.2    Nagengast, W.B.3
  • 97
    • 84866553587 scopus 로고    scopus 로고
    • Biomarkers that predict sensitivity to heat shock protein 90 inhibitors (HSP90i)
    • Suppl):abstract 10618
    • Jhaveri KL. Biomarkers that predict sensitivity to heat shock protein 90 inhibitors (HSP90i). J Clin Oncol 2012;30(Suppl):abstract 10618
    • (2012) J Clin Oncol , vol.30
    • Jhaveri, K.L.1
  • 98
    • 80054981928 scopus 로고    scopus 로고
    • Chemical biology: Many faces of a cancer-supporting protein
    • Darby JF, Workman P. Chemical biology: Many faces of a cancer-supporting protein. Nature 2011;478(7369):334-5
    • (2011) Nature , vol.478 , Issue.7369 , pp. 334-335
    • Darby, J.F.1    Workman, P.2
  • 99
    • 84884253288 scopus 로고    scopus 로고
    • Posttranslational modification and conformational state of heat shock protein 90 differentially affect binding of chemically diverse small molecule inhibitors
    • Beebe K, Mollapour M, Scroggins B, et al. Posttranslational modification and conformational state of heat shock protein 90 differentially affect binding of chemically diverse small molecule inhibitors. Oncotarget 2013;4(7):1065-74
    • (2013) Oncotarget , vol.4 , Issue.7 , pp. 1065-1074
    • Beebe, K.1    Mollapour, M.2    Scroggins, B.3


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