메뉴 건너뛰기




Volumn 69, Issue 4, 2012, Pages 901-909

Chidamide (CS055/HBI-8000): A new histone deacetylase inhibitor of the benzamide class with antitumor activity and the ability to enhance immune cell-mediated tumor cell cytotoxicity

Author keywords

Antitumor activity; Chidamide; HDAC inhibitor; Immune cell mediated cytotoxicity

Indexed keywords

ANTINEOPLASTIC AGENT; CHIDAMIDE; CS 055; HBI 8000; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 84859787650     PISSN: 03445704     EISSN: 14320843     Source Type: Journal    
DOI: 10.1007/s00280-011-1766-x     Document Type: Article
Times cited : (270)

References (25)
  • 1
    • 23644436275 scopus 로고    scopus 로고
    • Histone modifications as key regulators of transcription
    • Khan AU, Krishnamurthy S (2005) Histone modifications as key regulators of transcription. Front Biosci 10:866-872
    • (2005) Front Biosci , vol.10 , pp. 866-872
    • Khan, A.U.1    Krishnamurthy, S.2
  • 2
    • 64049097640 scopus 로고    scopus 로고
    • The promises and pitfalls of epigenetic therapies in solid tumours
    • Graham JS, Kaye SB, Brown R (2009) The promises and pitfalls of epigenetic therapies in solid tumours. Eur J Cancer 45:1129-1136
    • (2009) Eur J Cancer , vol.45 , pp. 1129-1136
    • Graham, J.S.1    Kaye, S.B.2    Brown, R.3
  • 3
    • 33746144518 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase class I but not class II is critical for the sensitization of leukemic cells to tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis
    • DOI 10.1158/0008-5472.CAN-05-4563
    • Inoue S, Mai A, Dyer MJ, Cohen GM (2006) Inhibition of histone deacetylase class I but not class II is critical for the sensitization of leukemic cells to tumour necrosis factor-related apoptosis-inducing ligand-induced apoptosis. Cancer Res 66:6785-6792 (Pubitemid 44085638)
    • (2006) Cancer Research , vol.66 , Issue.13 , pp. 6785-6792
    • Inoue, S.1    Mai, A.2    Dyer, M.J.S.3    Cohen, G.M.4
  • 5
    • 38949086502 scopus 로고    scopus 로고
    • Histone deacetylases 1, 2 and 3 are highly expressed in prostate cancer and HDAC2 expression is associated with shorter PSA relapse time after radical prostatectomy
    • DOI 10.1038/sj.bjc.6604199, PII 6604199
    • Weichert W, Röske A, Gekeler V, Beckers T, Stephan C, Jung K, Fritzsche FR, Niesporek S, Denkert C, Dietel M, Kristiansen G (2008) Histone deacetylases 1, 2 and 3 are highly expressed in prostate cancer and HDAC2 expression is associated with shorter PSA relapse time after radical prostatectomy. Br J Cancer 98:604-610 (Pubitemid 351214528)
    • (2008) British Journal of Cancer , vol.98 , Issue.3 , pp. 604-610
    • Weichert, W.1    Roske, A.2    Gekeler, V.3    Beckers, T.4    Stephan, C.5    Jung, K.6    Fritzsche, F.R.7    Niesporek, S.8    Denkert, C.9    Dietel, M.10    Kristiansen, G.11
  • 6
    • 39549088498 scopus 로고    scopus 로고
    • Class II histone deacetylases play pivotal roles in heat shock protein 90-mediated proteasomal degradation of vascular endothelial growth factor receptors
    • Park JH, Kim SH, Choi MC, Lee J, Oh DY, Im SA, Bang YJ, Kim TY (2008) Class II histone deacetylases play pivotal roles in heat shock protein 90-mediated proteasomal degradation of vascular endothelial growth factor receptors. Biochem Biophys Res Commun 368:318-322
    • (2008) Biochem Biophys Res Commun , vol.368 , pp. 318-322
    • Park, J.H.1    Kim, S.H.2    Choi, M.C.3    Lee, J.4    Oh, D.Y.5    Im, S.A.6    Bang, Y.J.7    Kim, T.Y.8
  • 8
    • 77955914870 scopus 로고    scopus 로고
    • Identification of type-specific anticancer histone deacetylase inhibitors: Road to success
    • Noureen N, Rashid H, Kalsoom S (2010) Identification of type-specific anticancer histone deacetylase inhibitors: road to success. Cancer Chemother Pharmacol 66(4):625-633
    • (2010) Cancer Chemother Pharmacol , vol.66 , Issue.4 , pp. 625-633
    • Noureen, N.1    Rashid, H.2    Kalsoom, S.3
  • 9
    • 84859791827 scopus 로고    scopus 로고
    • FDA (2006) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ZOLINZA™, NDA 21-991, Merck and Co. Inc. 6 Oct 2006
    • FDA (2006) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ZOLINZA™, NDA 21-991, Merck and Co. Inc. 6 Oct 2006
  • 10
    • 84859791829 scopus 로고    scopus 로고
    • FDA (2009) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ISTODAX, NDA 022393, Gloucester Pharmaceuticals. 5 Nov 2009
    • FDA (2009) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ISTODAX, NDA 022393, Gloucester Pharmaceuticals. 5 Nov 2009
  • 11
    • 84859798207 scopus 로고    scopus 로고
    • FDA (2011) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ISTODAX, NDA 022393/S-004, Celgene Corporation. 16 Jun 2011
    • FDA (2011) US Food and Drug Administration, Center for Drug Evaluation and Research, Office of Oncology Drug Products (OODP). Approval letter for ISTODAX, NDA 022393/S-004, Celgene Corporation. 16 Jun 2011
  • 16
    • 34447101115 scopus 로고    scopus 로고
    • MS-275, a potent orally available inhibitor of histone deacetylases-The development of an anticancer agent
    • DOI 10.1016/j.biocel.2007.02.009, PII S135727250700057X
    • Hess-Stumpp H, Bracker TU, Henderson D, Politz O (2007) MS-275, a potent orally available inhibitor of histone deacetylases-the development of an anticancer agent. Int J Biochem Cell Biol 39:1388-1405 (Pubitemid 47031032)
    • (2007) International Journal of Biochemistry and Cell Biology , vol.39 , Issue.7-8 , pp. 1388-1405
    • Hess-Stumpp, H.1    Bracker, T.U.2    Henderson, D.3    Politz, O.4
  • 19
    • 30344477367 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
    • DOI 10.1038/nrc1779
    • Minucci S, Pelicci PG (2006) Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 6:38-51 (Pubitemid 43054973)
    • (2006) Nature Reviews Cancer , vol.6 , Issue.1 , pp. 38-51
    • Minucci, S.1    Pelicci, P.G.2
  • 21
    • 13844250359 scopus 로고    scopus 로고
    • Development of a PAN-specific, affinity-purified anti-acetylated lysine antibody for detection, identification, isolation, and intracellular localization of acetylated protein
    • DOI 10.1081/IAS-200041153
    • Qiang L, Xiao H, Campos EI, Ho VC, Li G (2005) Development of a PAN-specific, affinity-purified antiacetylated lysine antibody for detection, identification, isolation, and intracellular localization of acetylated protein. J Immunoass Immunochem 26:13-23 (Pubitemid 40250342)
    • (2005) Journal of Immunoassay and Immunochemistry , vol.26 , Issue.1 , pp. 13-23
    • Qiang, L.1    Xiao, H.2    Campos, E.I.3    Ho, V.C.4    Li, G.5
  • 22
    • 34547094822 scopus 로고    scopus 로고
    • Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group
    • DOI 10.1002/ijc.22751
    • Beckers T, Burkhardt C, Wieland H, Gimmnich P, Ciossek T, Maier T, Sanders K (2007) Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group. Int J Cancer 121:1138-1148 (Pubitemid 47101654)
    • (2007) International Journal of Cancer , vol.121 , Issue.5 , pp. 1138-1148
    • Beckers, T.1    Burkhardt, C.2    Wieland, H.3    Gimmnich, P.4    Ciossek, T.5    Maier, T.6    Sanders, K.7
  • 24
    • 28244502269 scopus 로고    scopus 로고
    • Cancer cells become susceptible to natural killer cell killing after exposure to histone deacetylase inhibitors due to glycogen synthase kinase-3-dependent expression of MHC class I-related chain A and B
    • DOI 10.1158/0008-5472.CAN-05-0599
    • Skov S, Pedersen MT, Andresen L, Straten PT, Woetmann A, Odum N (2005) Cancer cells become susceptible to natural killer cell killing after exposure to histone deacetylase inhibitors due to glycogen synthase kinase-3-dependent expression of MHC class I-related chain A and B. Cancer Res 65:11136-11145 (Pubitemid 41713385)
    • (2005) Cancer Research , vol.65 , Issue.23 , pp. 11136-11145
    • Skov, S.1    Pedersen, M.T.2    Andresen, L.3    Straten, P.T.4    Woetmann, A.5    Odum, N.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.