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Volumn 2, Issue 3, 2010, Pages 457-465

Targeting histone deacetylases: Development of vorinostat for the treatment of cancer

Author keywords

cancer therapeutic; chromatin modifying enzymes; histone deacetylase; protein acetylation; vorinostat

Indexed keywords

5 AZA 2' DEOXYCYTIDINE; AZACITIDINE; BELINOSTAT; BENZAMIDE; BEVACIZUMAB; BORTEZOMIB; CARBOPLATIN; CISPLATIN; CYTOTOXIC AGENT; DEXAMETHASONE; ENTINOSTAT; ERLOTINIB; FLUOROURACIL; GEMCITABINE; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; LENALIDOMIDE; MELPHALAN; MOCETINOSTAT; N (2 AMINOPHENYL) 4 (3 PYRIDINYLMETHOXYCARBONYLAMINOMETHYL)BENZAMIDE; N (2 AMINOPHENYL) 4 [4 (3 PYRIDINYL) 2 PYRIMIDINYLAMINOMETHYL]BENZAMIDE; PACLITAXEL; PANOBINOSTAT; PREDNISONE; PROTEASOME INHIBITOR; PROTEIN TYROSINE KINASE INHIBITOR; ROMIDEPSIN; SALINOSPORAMIDE A; SNDX 275; UNCLASSIFIED DRUG; UNINDEXED DRUG; VORINOSTAT;

EID: 77954100842     PISSN: 17501911     EISSN: 1750192X     Source Type: Journal    
DOI: 10.2217/epi.10.20     Document Type: Review
Times cited : (20)

References (73)
  • 1
    • 1542588471 scopus 로고    scopus 로고
    • Second generation hybrid polar compounds are potent inducers of transformed cell differentiation
    • Richon VM, Webb Y, Merger R et al.: Second generation hybrid polar compounds are potent inducers of transformed cell differentiation. Proc. Natl Acad. Sci. USA 93(12), 5705-5708 (1996).
    • (1996) Proc. Natl Acad. Sci. USA , vol.93 , Issue.12 , pp. 5705-5708
    • Richon, V.M.1    Webb, Y.2    Merger, R.3
  • 2
    • 0032539890 scopus 로고    scopus 로고
    • A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
    • Richon VM, Emiliani S, Verdin E et al.: A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. Proc. Natl Acad. Sci. USA 95(6), 3003-3007 (1998).
    • (1998) Proc. Natl Acad. Sci. USA , vol.95 , Issue.6 , pp. 3003-3007
    • Richon, V.M.1    Emiliani, S.2    Verdin, E.3
  • 4
    • 67349095775 scopus 로고    scopus 로고
    • Development of vorinostat: Current applications and future perspectives for cancer therapy
    • Richon VM, Garcia-Vargas J, Hardwick JS: Development of vorinostat: current applications and future perspectives for cancer therapy. Cancer Lett. 280(2), 201-210 (2009).
    • (2009) Cancer Lett. , vol.280 , Issue.2 , pp. 201-210
    • Richon, V.M.1    Garcia-Vargas, J.2    Hardwick, J.S.3
  • 5
    • 39749127166 scopus 로고    scopus 로고
    • The Rpd3/Hda1 family of lysine deacetylases: From bacteria and yeast to mice and men
    • Yang XJ, Seto E: The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men. Nat. Rev Mol. Cell Biol. 9, 206-218 (2008).
    • (2008) Nat. Rev Mol. Cell Biol. , vol.9 , pp. 206-218
    • Yang, X.J.1    Seto, E.2
  • 6
    • 68949212379 scopus 로고    scopus 로고
    • Lysine acetylation targets protein complexes and co-regulates major cellular functions
    • Choudhary C, Kumar C, Gnad F et al.: Lysine acetylation targets protein complexes and co-regulates major cellular functions. Science 325(5942), 834-840 (2009).
    • (2009) Science , vol.325 , Issue.5942 , pp. 834-840
    • Choudhary, C.1    Kumar, C.2    Gnad, F.3
  • 7
    • 77649138161 scopus 로고    scopus 로고
    • Screening for therapeutic targets of vorinostat by SILAC-based proteomic analysis in human breast cancer cells
    • Zhou Q, Chaerkady R, Shaw PG, Kensler TW, Pandey A, Davidson NE: Screening for therapeutic targets of vorinostat by SILAC-based proteomic analysis in human breast cancer cells. Proteomics 10(5), 1029-1039 (2010).
    • (2010) Proteomics , vol.10 , Issue.5 , pp. 1029-1039
    • Zhou, Q.1    Chaerkady, R.2    Shaw, P.G.3    Kensler, T.W.4    Pandey, A.5    Davidson, N.E.6
  • 8
    • 0034104047 scopus 로고    scopus 로고
    • Mutations truncating the EP300 acetylase in human cancers
    • Gayther SA, Batley SJ, Linger L et al.: Mutations truncating the EP300 acetylase in human cancers. Nat. Genet. 24(3), 300-303 (2000).
    • (2000) Nat. Genet. , vol.24 , Issue.3 , pp. 300-303
    • Gayther, S.A.1    Batley, S.J.2    Linger, L.3
  • 9
    • 0035676731 scopus 로고    scopus 로고
    • Expression profle of histone deacetylase 1 in gastric cancer tissues
    • Choi JH, Kwon HJ, Yoon BI et al.: Expression profle of histone deacetylase 1 in gastric cancer tissues. Jpn. J. Cancer Res. 92(12), 1300-1304 (2001).
    • (2001) Jpn. J. Cancer Res. , vol.92 , Issue.12 , pp. 1300-1304
    • Choi, J.H.1    Kwon, H.J.2    Yoon, B.I.3
  • 10
    • 1842631408 scopus 로고    scopus 로고
    • Upregulation and nuclear recruitment of HDAC1 in hormone refractory prostate cancer
    • Halkidou K, Gaughan L, Cook S, Leung HY, Neal DE, Robson CN: Upregulation and nuclear recruitment of HDAC1 in hormone refractory prostate cancer. Prostate 59(2), 177-189 (2004).
    • (2004) Prostate , vol.59 , Issue.2 , pp. 177-189
    • Halkidou, K.1    Gaughan, L.2    Cook, S.3    Leung, H.Y.4    Neal, D.E.5    Robson, C.N.6
  • 12
    • 77949743508 scopus 로고    scopus 로고
    • Expression profle of histone deacetylases 1, 2 and 3 in ovarian cancer tissues
    • Jin KL, Pak JH, Park JY et al.: Expression profle of histone deacetylases 1, 2 and 3 in ovarian cancer tissues. J. Gynecol. Oncol. 19(3), 185-190 (2008).
    • (2008) J. Gynecol. Oncol. , vol.19 , Issue.3 , pp. 185-190
    • Jin, K.L.1    Pak, J.H.2    Park, J.Y.3
  • 13
    • 67449100866 scopus 로고    scopus 로고
    • Histone deacetylase 2 expression predicts poorer prognosis in oral cancer patients
    • Chang HH, Chiang CP, Hung HC, Lin CY, Deng Y T, Kuo MY: Histone deacetylase 2 expression predicts poorer prognosis in oral cancer patients. Oral Oncol. 45(7), 610-614 (2009).
    • (2009) Oral Oncol. , vol.45 , Issue.7 , pp. 610-614
    • Chang, H.H.1    Chiang, C.P.2    Hung, H.C.3    Lin, C.Y.4    Deng, Y.T.5    Kuo, M.Y.6
  • 14
    • 0032531688 scopus 로고    scopus 로고
    • The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression
    • Dhordain P, Lin RJ, Quief S et al.: The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression. Nucleic Acids Res. 26(20), 4645-4651 (1998).
    • (1998) Nucleic Acids Res. , vol.26 , Issue.20 , pp. 4645-4651
    • Dhordain, P.1    Lin, R.J.2    Quief, S.3
  • 15
    • 17144458786 scopus 로고    scopus 로고
    • Fusion proteins of the retinoic acid receptor-a recruit histone deacetylase in promyelocytic leukaemia
    • Grignani F, De Matteis S, Nervi C et al.: Fusion proteins of the retinoic acid receptor-a recruit histone deacetylase in promyelocytic leukaemia. Nature 391(6669), 815-818 (1998).
    • (1998) Nature , vol.391 , Issue.6669 , pp. 815-818
    • Grignani, F.1    De Matteis, S.2    Nervi, C.3
  • 16
    • 33646354640 scopus 로고    scopus 로고
    • A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition
    • Ropero S, Fraga MF, Ballestar E et al.: A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition. Nat. Genet. 38(5), 566-569 (2006).
    • (2006) Nat. Genet. , vol.38 , Issue.5 , pp. 566-569
    • Ropero, S.1    Fraga, M.F.2    Ballestar, E.3
  • 17
    • 55249098844 scopus 로고    scopus 로고
    • An inactivating mutation in HDAC2 leads to dysregulation of apoptosis mediated by APAF1
    • Hanigan CL, van Engeland M, De Bruine AP et al.: An inactivating mutation in HDAC2 leads to dysregulation of apoptosis mediated by APAF1. Gastroenterology 135(5), 1654-1664.e2 (2008).
    • (2008) Gastroenterology , vol.135 , Issue.5 , pp. 1654-1664
    • Hanigan, C.L.1    Van Engeland, M.2    De Bruine, A.P.3
  • 19
    • 17144378591 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1
    • Huang BH, Laban M, Leung CH et al.: Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1. Cell Death Differ. 12(4), 395-404 (2005).
    • (2005) Cell Death Differ. , vol.12 , Issue.4 , pp. 395-404
    • Huang, B.H.1    Laban, M.2    Lee, C.H.3
  • 20
    • 34347339526 scopus 로고    scopus 로고
    • Role for histone deacetylase 1 in human tumor cell proliferation
    • Senese S, Zaragoza K, Minardi S et al.: Role for histone deacetylase 1 in human tumor cell proliferation. Mol. Cell Biol. 27(13), 4784-4795 (2007).
    • (2007) Mol. Cell Biol. , vol.27 , Issue.13 , pp. 4784-4795
    • Senese, S.1    Zaragoza, K.2    Minardi, S.3
  • 21
    • 67449138841 scopus 로고    scopus 로고
    • Epigenetic modifers: Basic understanding and clinical development
    • Piekarz RL, Bates SE: Epigenetic modifers: basic understanding and clinical development. Clin. Cancer Res. 15(12), 3918-3926 (2009).
    • (2009) Clin. Cancer Res. , vol.15 , Issue.12 , pp. 3918-3926
    • Piekarz, R.L.1    Bates, S.E.2
  • 22
    • 77249087051 scopus 로고    scopus 로고
    • Chemical phylogenetics of histone deacetylases
    • Bradner JE, West N, Grachan ML et al.: Chemical phylogenetics of histone deacetylases. Nat. Chem. Biol. 6(3), 238-243 (2010).
    • (2010) Nat. Chem. Biol. , vol.6 , Issue.3 , pp. 238-243
    • Bradner, J.E.1    West, N.2    Grachan, M.L.3
  • 23
    • 34547683194 scopus 로고    scopus 로고
    • Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma
    • Olsen EA, Kim YH, Kuzel TM et al.: Phase IIb multicenter trial of vorinostat in patients with persistent, progressive, or treatment refractory cutaneous T-cell lymphoma. J. Clin. Oncol. 25(21), 3109-3115 (2007).
    • (2007) J. Clin. Oncol. , vol.25 , Issue.21 , pp. 3109-3115
    • Olsen, E.A.1    Kim, Y.H.2    Kuzel, T.M.3
  • 24
    • 77749309291 scopus 로고    scopus 로고
    • Romidepsin for the treatment of cutaneous T-cell lymphoma
    • Campas-Moya C: Romidepsin for the treatment of cutaneous T-cell lymphoma. Drugs Today (Barc.) 45(11), 787-795 (2009).
    • (2009) Drugs Today (Barc.) , vol.45 , Issue.11 , pp. 787-795
    • Campas-Moya, C.1
  • 25
    • 0042905956 scopus 로고    scopus 로고
    • Gene expression profling of multiple histone deacetylase (HDAC) inhibitors: Defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
    • Glaser KB, Staver MJ, Waring JF, Stender J, Ulrich RG, Davidsen SK: Gene expression profling of multiple histone deacetylase (HDAC) inhibitors: defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines. Mol. Cancer Ther. 2(2), 151-163 (2003).
    • (2003) Mol. Cancer Ther. , vol.2 , Issue.2 , pp. 151-163
    • Glaser, K.B.1    Staver, M.J.2    Waring, J.F.3    Stender, J.4    Ulrich, R.G.5    Davidsen, S.K.6
  • 26
    • 9144220841 scopus 로고    scopus 로고
    • Transcriptional signature of histone deacetylase inhibition in multiple myeloma: Biological and clinical implications
    • Mitsiades CS, Mitsiades NS, McMullan CJ et al.: Transcriptional signature of histone deacetylase inhibition in multiple myeloma: biological and clinical implications. Proc. Natl Acad. Sci. USA 101(2), 540-545 (2004).
    • (2004) Proc. Natl Acad. Sci. USA , vol.101 , Issue.2 , pp. 540-545
    • Mitsiades, C.S.1    Mitsiades, N.S.2    McMullan, C.J.3
  • 27
    • 14844353574 scopus 로고    scopus 로고
    • Identifcation and functional signifcance of genes regulated by structurally different histone deacetylase inhibitors
    • Peart MJ, Smyth GK, van Laar RK et al.: Identifcation and functional signifcance of genes regulated by structurally different histone deacetylase inhibitors. Proc. Natl Acad. Sci. USA 102(10), 3697-3702 (2005).
    • (2005) Proc. Natl Acad. Sci. USA , vol.102 , Issue.10 , pp. 3697-3702
    • Peart, M.J.1    Smyth, G.K.2    Van Laar, R.K.3
  • 28
    • 74349116248 scopus 로고    scopus 로고
    • DNA microarray profling of genes differentially regulated by the histone deacetylase inhibitors vorinostat and LBH589 in colon cancer cell lines
    • LaBonte MJ, Wilson PM, Fazzone W, Groshen S, Lenz HJ, Ladner RD: DNA microarray profling of genes differentially regulated by the histone deacetylase inhibitors vorinostat and LBH589 in colon cancer cell lines. BMC Med. Genomics 2, 67 (2009).
    • (2009) BMC Med. Genomics , vol.2 , pp. 67
    • Labonte, M.J.1    Wilson, P.M.2    Fazzone, W.3    Groshen, S.4    Lenz, H.J.5    Ladner, R.D.6
  • 29
    • 0035694469 scopus 로고    scopus 로고
    • Acetylation of p53 activates transcription through recruitment of coactivators/histone acetyltransferases
    • Barlev NA, Liu L, Chehab NH et al.: Acetylation of p53 activates transcription through recruitment of coactivators/histone acetyltransferases. Mol. Cell. 8(6), 1243-1254 (2001).
    • (2001) Mol. Cell. , vol.8 , Issue.6 , pp. 1243-1254
    • Barlev, N.A.1    Liu, L.2    Chehab, N.H.3
  • 30
    • 0036898253 scopus 로고    scopus 로고
    • Acetylation inactivates the transcriptional repressor BCL6
    • Bereshchenko OR, Gu W, Dalla-Favera R: Acetylation inactivates the transcriptional repressor BCL6. Nat. Genet. 32(4), 606-613 (2002).
    • (2002) Nat. Genet. , vol.32 , Issue.4 , pp. 606-613
    • Bereshchenko, O.R.1    Gu, W.2    Dalla-Favera, R.3
  • 31
    • 15744385061 scopus 로고    scopus 로고
    • Activation of Stat3 sequence-specifc DNA binding and transcription by p300/CREB-binding protein-mediated acetylation
    • Wang R, Cherukuri P, Luo J: Activation of Stat3 sequence-specifc DNA binding and transcription by p300/CREB-binding protein-mediated acetylation. J. Biol. Chem. 280(12), 11528-11534 (2005).
    • (2005) J. Biol. Chem. , vol.280 , Issue.12 , pp. 11528-11534
    • Wang, R.1    Cherukuri, P.2    Luo, J.3
  • 32
    • 67349285731 scopus 로고    scopus 로고
    • Enhancing the apoptotic and therapeutic effects of HDAC inhibitors
    • Frew AJ, Johnstone RW, Bolden JE: Enhancing the apoptotic and therapeutic effects of HDAC inhibitors. Cancer Lett. 280(2), 125-133 (2009).
    • (2009) Cancer Lett. , vol.280 , Issue.2 , pp. 125-133
    • Frew, A.J.1    Johnstone, R.W.2    Bolden, J.E.3
  • 33
    • 11144221007 scopus 로고    scopus 로고
    • Apoptotic and autophagic cell death induced by histone deacetylase inhibitors
    • Shao Y, Gao Z, Marks PA, Jiang X: Apoptotic and autophagic cell death induced by histone deacetylase inhibitors. Proc. Natl Acad. Sci. USA 101(52), 18030-18035 (2004).
    • (2004) Proc. Natl Acad. Sci. USA , vol.101 , Issue.52 , pp. 18030-18035
    • Shao, Y.1    Gao, Z.2    Marks, P.A.3    Jiang, X.4
  • 34
    • 85047699941 scopus 로고    scopus 로고
    • Histone deacetylases inhibitors as anti-angiogenic agents altering vascular endothelial growth factor signaling
    • Deroanne CF, Bonjean K, Servotte S et al.: Histone deacetylases inhibitors as anti-angiogenic agents altering vascular endothelial growth factor signaling. Oncogene 21(3), 427-436 (2002).
    • (2002) Oncogene , vol.21 , Issue.3 , pp. 427-436
    • Deroanne, C.F.1    Bonjean, K.2    Servotte, S.3
  • 35
    • 0033367018 scopus 로고    scopus 로고
    • Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA)
    • Cohen LA, Amin S, Marks PA, Rifkind RA, Desai D, Richon VM: Chemoprevention of carcinogen-induced mammary tumorigenesis by the hybrid polar cytodifferentiation agent, suberanilohydroxamic acid (SAHA). Anticancer Res. 19(6B), 4999-5005 (1999).
    • (1999) Anticancer Res. , vol.19 , Issue.6 B , pp. 4999-5005
    • Cohen, L.A.1    Amin, S.2    Marks, P.A.3    Rifkind, R.A.4    Desai, D.5    Richon, V.M.6
  • 36
    • 0036323115 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, suppresses the growth of carcinogen-induced mammary tumors
    • Cohen LA, Marks PA, Rifkind RA et al.: Suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, suppresses the growth of carcinogen-induced mammary tumors. Anticancer Res. 22(3), 1497-1504 (2002).
    • (2002) Anticancer Res. , vol.22 , Issue.3 , pp. 1497-1504
    • Cohen, L.A.1    Marks, P.A.2    Rifkind, R.A.3
  • 37
    • 0037236445 scopus 로고    scopus 로고
    • Chemopreventive effcacy of suberoylanilide hydroxamic acid (SAHA) against 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in female A/J mice
    • Desai D, Das A, Cohen L, el-Bayoumy K, Amin S: Chemopreventive effcacy of suberoylanilide hydroxamic acid (SAHA) against 4-(methylnitrosamino)-1-(3- pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in female A/J mice. Anticancer Res. 23(1A), 499-503 (2003).
    • (2003) Anticancer Res. , vol.23 , Issue.1 A , pp. 499-503
    • Desai, D.1    Das, A.2
  • 38
    • 0034665124 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
    • Butler LM, Agus DB, Scher HI et al.: Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res. 60(18), 5165-5170 (2000).
    • (2000) Cancer Res. , vol.60 , Issue.18 , pp. 5165-5170
    • Butler, L.M.1    Agus, D.B.2    Scher, H.I.3
  • 39
    • 33748581975 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid is effective in preclinical studies of medulloblastoma
    • Spiller SE, Ravanpay AC, Hahn AW, Olson JM: Suberoylanilide hydroxamic acid is effective in preclinical studies of medulloblastoma. J. Neurooncol. 79(3), 259-270 (2006).
    • (2006) J. Neurooncol. , vol.79 , Issue.3 , pp. 259-270
    • Spiller, S.E.1    Ravanpay, A.C.2    Hahn, A.W.3    Olson, J.M.4
  • 40
    • 67449089565 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors suppress thymidylate synthase gene expression and synergize with the fuoropyrimidines in colon cancer cells
    • Fazzone W, Wilson PM, Labonte MJ, Lenz HJ, Ladner RD: Histone deacetylase inhibitors suppress thymidylate synthase gene expression and synergize with the fuoropyrimidines in colon cancer cells. Int. J. Cancer 125(2), 463-473 (2009).
    • (2009) Int. J. Cancer , vol.125 , Issue.2 , pp. 463-473
    • Fazzone, W.1    Wilson, P.M.2    Labonte, M.J.3    Lenz, H.J.4    Ladner, R.D.5
  • 42
    • 0035189761 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors induce remission in transgenic models of therapy-resistant acute promyelocytic leukemia
    • He LZ, Tolentino T, Grayson P et al.: Histone deacetylase inhibitors induce remission in transgenic models of therapy-resistant acute promyelocytic leukemia. J. Clin. Invest. 108(9), 1321-1330 (2001).
    • (2001) J. Clin. Invest. , vol.108 , Issue.9 , pp. 1321-1330
    • He, L.Z.1    Tolentino, T.2    Grayson, P.3
  • 43
    • 34249941680 scopus 로고    scopus 로고
    • Analysis of the apoptotic and therapeutic activities of histone deacetylase inhibitors by using a mouse model of B cell lymphoma
    • Lindemann RK, Newbold A, Whitecross KF et al.: Analysis of the apoptotic and therapeutic activities of histone deacetylase inhibitors by using a mouse model of B cell lymphoma. Proc. Natl Acad. Sci. USA 104(19), 8071-8076 (2007).
    • (2007) Proc. Natl Acad. Sci. USA , vol.104 , Issue.19 , pp. 8071-8076
    • Lindemann, R.K.1    Newbold, A.2    Whitecross, K.F.3
  • 44
    • 77949886046 scopus 로고    scopus 로고
    • Nonclinical safety assessment of the histone deacetylase inhibitor vorinostat
    • Kerr JS, Galloway S, Lagrutta A et al.: Nonclinical safety assessment of the histone deacetylase inhibitor vorinostat. Int. J. Toxicol. 29(1), 3-19 (2010).
    • (2010) Int. J. Toxicol. , vol.29 , Issue.1 , pp. 3-19
    • Kerr, J.S.1    Galloway, S.2    Lagrutta, A.3
  • 45
    • 67449145358 scopus 로고    scopus 로고
    • Rational combinations using HDAC inhibitors
    • Bots M, Johnstone RW: Rational combinations using HDAC inhibitors. Clin. Cancer Res. 15(12), 3970-3977 (2009).
    • (2009) Clin. Cancer Res. , vol.15 , Issue.12 , pp. 3970-3977
    • Bots, M.1    Johnstone, R.W.2
  • 46
    • 31344466008 scopus 로고    scopus 로고
    • DNA methylation and gene silencing in cancer
    • Baylin SB: DNA methylation and gene silencing in cancer. Nat. Clin. Pract. Oncol. 2(Suppl. 1), S4-S11 (2005).
    • (2005) Nat. Clin. Pract. Oncol. , vol.2 , Issue.SUPPL. 1
    • Baylin, S.B.1
  • 47
    • 0032948005 scopus 로고    scopus 로고
    • Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer
    • Cameron EE, Bachman KE, Myöhänen S, Herman JG, Baylin SB: Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer. Nat. Genet. 21(1), 103-107 (1999).
    • (1999) Nat. Genet. , vol.21 , Issue.1 , pp. 103-107
    • Cameron, E.E.1    Bachman, K.E.2    Myöhänen, S.3    Herman, J.G.4    Baylin, S.B.5
  • 48
    • 34250810709 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor, suberoylanilide hydroxamic acid (vorinostat, SAHA) profoundly inhibits the growth of human pancreatic cancer cells
    • Kumagai T, Wakimoto N, Yin D et al.: Histone deacetylase inhibitor, suberoylanilide hydroxamic acid (vorinostat, SAHA) profoundly inhibits the growth of human pancreatic cancer cells. Int. J. Cancer 121(3), 656-665 (2007).
    • (2007) Int. J. Cancer , vol.121 , Issue.3 , pp. 656-665
    • Kumagai, T.1    Wakimoto, N.2    Yin, D.3
  • 49
    • 34248325147 scopus 로고    scopus 로고
    • Epigenetic combination therapy as a tumor-selective treatment approach for hepatocellular carcinoma
    • Venturelli S, Armeanu S, Pathil A: Epigenetic combination therapy as a tumor-selective treatment approach for hepatocellular carcinoma. Cancer 109(10), 2132-2141 (2007).
    • (2007) Cancer , vol.109 , Issue.10 , pp. 2132-2141
    • Venturelli, S.1    Armeanu, S.2    Pathil, A.3
  • 50
    • 52949085309 scopus 로고    scopus 로고
    • A Phase I/II study of vorinostat, an oral histone deacetylase inhibitor, in combination with azacitidine in patients with the myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Initial results of the Phase i trial: A New York cancer consortium study
    • ASCO Meeting Abstracts
    • Silverman LB, Verma A, Odchimar-Ressig R et al.: A Phase I/II study of vorinostat, an oral histone deacetylase inhibitor, in combination with azacitidine in patients with the myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Initial results of the Phase I trial: a New York cancer consortium study. J. Clin Oncol. 26, 7000 (2008) (ASCO Meeting Abstracts).
    • (2008) J. Clin Oncol. , vol.26 , pp. 7000
    • Silverman, L.B.1    Verma, A.2    Odchimar-Ressig, R.3
  • 51
    • 68149172699 scopus 로고    scopus 로고
    • Modulation of thymidilate synthase and p53 expression by HDAC inhibitor vorinostat resulted in synergistic anti-tumor effect in combination with 5FU or raltitrexed
    • DiGennaro E, Bruzzese F, Pepe S et al.: Modulation of thymidilate synthase and p53 expression by HDAC inhibitor vorinostat resulted in synergistic anti-tumor effect in combination with 5FU or raltitrexed. Cancer Biol. Ther. 8(9), 782-791 (2009).
    • (2009) Cancer Biol. Ther. , vol.8 , Issue.9 , pp. 782-791
    • Digennaro, E.1    Bruzzese, F.2    Pepe, S.3
  • 52
    • 65649107307 scopus 로고    scopus 로고
    • A Phase I, pharmacokinetic and pharmacodynamic study on vorinostat in combination with 5-fuorouracil, leucovorin, and oxaliplatin in patients with refractory colorectal cancer
    • Fakih MG, Pendyala L, Fetterly G et al.: A Phase I, pharmacokinetic and pharmacodynamic study on vorinostat in combination with 5-fuorouracil, leucovorin, and oxaliplatin in patients with refractory colorectal cancer. Clin. Cancer Res. 15(9), 3189-3195 (2009).
    • (2009) Clin. Cancer Res. , vol.15 , Issue.9 , pp. 3189-3195
    • Fakih, M.G.1    Pendyala, L.2    Fetterly, G.3
  • 53
    • 77649183822 scopus 로고    scopus 로고
    • A Phase I/II trial of vorinostat in combination with 5-fuorouracil in patients with metastatic colorectal cancer who previously failed 5-FU-based chemotherapy
    • Wilson PM, El-Khoueiry A, Iqbal S et al.: A Phase I/II trial of vorinostat in combination with 5-fuorouracil in patients with metastatic colorectal cancer who previously failed 5-FU-based chemotherapy. Cancer Chemother. Pharmacol. 65(5), 979-988 (2010).
    • (2010) Cancer Chemother. Pharmacol. , vol.65 , Issue.5 , pp. 979-988
    • Wilson, P.M.1    El-Khoueiry, A.2    Iqbal, S.3
  • 55
    • 2342667387 scopus 로고    scopus 로고
    • The development of proteasome inhibitors as anticancer drugs
    • Adams J: The development of proteasome inhibitors as anticancer drugs. Cancer Cell 5(5), 417-421 (2004).
    • (2004) Cancer Cell , vol.5 , Issue.5 , pp. 417-421
    • Adams, J.1
  • 56
    • 33645737411 scopus 로고    scopus 로고
    • Aggresome disruption: A novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells
    • Nawrocki ST, Carew JS, Pino MS et al.: Aggresome disruption: a novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells. Cancer Res. 66, 3773-3781 (2006).
    • (2006) Cancer Res. , vol.66 , pp. 3773-3781
    • Nawrocki, S.T.1    Carew, J.S.2    Pino, M.S.3
  • 57
    • 0346020435 scopus 로고    scopus 로고
    • The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress
    • Kawaguchi Y, Kovacs JJ, McLaurin A, Vance JM, Ito A, Yao TP: The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress. Cell 115(6), 727-738 (2003).
    • (2003) Cell , vol.115 , Issue.6 , pp. 727-738
    • Kawaguchi, Y.1    Kovacs, J.J.2    McLaurin, A.3    Vance, J.M.4    Ito, A.5    Yao, T.P.6
  • 58
    • 6344229760 scopus 로고    scopus 로고
    • Proteasome inhibition sensitizes non-small cell lung cancer to histone deacetylase inhibitor-induced apoptosis through the generation of reactive oxygen species
    • Denlinger CE, Rundall BK, Jones DR: Proteasome inhibition sensitizes non-small cell lung cancer to histone deacetylase inhibitor-induced apoptosis through the generation of reactive oxygen species. J. Thorac. Cardiovasc. Surg. 128(5), 740-748 (2004).
    • (2004) J. Thorac. Cardiovasc. Surg. , vol.128 , Issue.5 , pp. 740-748
    • Denlinger, C.E.1    Rundall, B.K.2    Jones, D.R.3
  • 59
    • 2542523228 scopus 로고    scopus 로고
    • Synergistic induction of oxidative injury and apoptosis in human multiple myeloma cells by the proteasome inhibitor bortezomib and histone deacetylase inhibitors
    • Pei XY, Dai Y, Grant S: Synergistic induction of oxidative injury and apoptosis in human multiple myeloma cells by the proteasome inhibitor bortezomib and histone deacetylase inhibitors. Clin. Cancer Res. 10(11), 3839-3852 (2004).
    • (2004) Clin. Cancer Res. , vol.10 , Issue.11 , pp. 3839-3852
    • Pei, X.Y.1    Dai, Y.2    Grant, S.3
  • 60
    • 0242493856 scopus 로고    scopus 로고
    • The proteasome inhibitor bortezomib interacts synergistically with histone deacetylase inhibitors to induce apoptosis in Bcr/Abl+ cells sensitive and resistant to STI571
    • Yu C, Rahmani M, Conrad D, Subler M, Dent P, Grant S: The proteasome inhibitor bortezomib interacts synergistically with histone deacetylase inhibitors to induce apoptosis in Bcr/Abl+ cells sensitive and resistant to STI571. Blood 102(10), 3765-3774 (2003).
    • (2003) Blood , vol.102 , Issue.10 , pp. 3765-3774
    • Yu, C.1    Rahmani, M.2    Conrad, D.3    Subler, M.4    Dent, P.5    Grant, S.6
  • 61
    • 69349097803 scopus 로고    scopus 로고
    • Phase i study of vorinostat in combination with bortezomib for relapsed and refractory multiple myeloma
    • Badros A, Burger AM, Philip S et al.: Phase I study of vorinostat in combination with bortezomib for relapsed and refractory multiple myeloma. Clin. Cancer Res. 15(16), 5250-5257 (2009).
    • (2009) Clin. Cancer Res. , vol.15 , Issue.16 , pp. 5250-5257
    • Badros, A.1    Burger, A.M.2    Philip, S.3
  • 62
    • 69249209745 scopus 로고    scopus 로고
    • Vorinostat in solid and hematologic malignancies
    • Siegel D, Hussein M, Belani C et al.: Vorinostat in solid and hematologic malignancies. J. Hematol. Oncol. 2, 31 (2009).
    • (2009) J. Hematol. Oncol. , vol.2 , pp. 31
    • Siegel, D.1    Hussein, M.2    Belani, C.3
  • 63
    • 77649171884 scopus 로고    scopus 로고
    • Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents
    • Tan J, Cang S, Ma Y, Petrillo RL, Liu D: Novel histone deacetylase inhibitors in clinical trials as anti-cancer agents. J. Hematol. Oncol. 3, 5 (2010).
    • J. Hematol. Oncol. , vol.3 , Issue.5 , pp. 2010
    • Tan, J.1    Cang, S.2    Ma, Y.3    Petrillo, R.L.4    Liu, D.5
  • 64
    • 67651153048 scopus 로고    scopus 로고
    • New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer
    • Cang S, Ma Y, Liu D: New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer. J. Hematol. Oncol. 2, 22 (2009).
    • (2009) J. Hematol. Oncol. , vol.2 , pp. 22
    • Cang, S.1    Ma, Y.2    Liu, D.3
  • 65
    • 72549108593 scopus 로고    scopus 로고
    • A single supratherapeutic dose of vorinostat does not prolong the QTc interval in patients with advanced cancer
    • Munster PN, Rubin EH, van Belle S et al.: A single supratherapeutic dose of vorinostat does not prolong the QTc interval in patients with advanced cancer. Clin. Cancer Res. 15(22), 7077-7084 (2009).
    • (2009) Clin. Cancer Res. , vol.15 , Issue.22 , pp. 7077-7084
    • Munster, P.N.1    Rubin, E.H.2    Van Belle, S.3
  • 66
    • 21244464349 scopus 로고    scopus 로고
    • Phase i study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer
    • Kelly WK, O'Connor OA, Krug LM et al.: Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J. Clin. Oncol. 23, 3923-3931 (2005).
    • (2005) J. Clin. Oncol. , vol.23 , pp. 3923-3931
    • Kelly, W.K.1    O'Connor, O.A.2    Krug, L.M.3
  • 67
    • 33644836549 scopus 로고    scopus 로고
    • Clinical experience with intravenous and oral formulations of the novel histone deacetylase inhibitor suberoylanilide hydroxamic acid in patients with advanced hematologic malignancies
    • O'Connor OA, Heaney ML, Schwartz L et al.: Clinical experience with intravenous and oral formulations of the novel histone deacetylase inhibitor suberoylanilide hydroxamic acid in patients with advanced hematologic malignancies. J. Clin. Oncol. 24(1), 166-173 (2006).
    • (2006) J. Clin. Oncol. , vol.24 , Issue.1 , pp. 166-173
    • O'Connor, O.A.1    Heaney, M.L.2    Schwartz, L.3
  • 68
    • 38949096781 scopus 로고    scopus 로고
    • Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes
    • Garcia-Manero G, Yang H, Bueso-Ramos C et al.: Phase 1 study of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid [SAHA]) in patients with advanced leukemias and myelodysplastic syndromes. Blood 111(3), 1060-1066 (2008).
    • (2008) Blood , vol.111 , Issue.3 , pp. 1060-1066
    • Garcia-Manero, G.1    Yang, H.2    Bueso-Ramos, C.3
  • 69
    • 65349141942 scopus 로고    scopus 로고
    • Phase II trial of vorinostat in recurrent glioblastoma multiforme: A north central cancer treatment group study
    • Galanis E, Jaeckle KA, Maurer MJ et al.: Phase II trial of vorinostat in recurrent glioblastoma multiforme: a north central cancer treatment group study. J. Clin. Oncol. 27(12), 2052-2058 (2009).
    • (2009) J. Clin. Oncol. , vol.27 , Issue.12 , pp. 2052-2058
    • Galanis, E.1    Jaeckle, K.A.2    Maurer, M.J.3
  • 70
    • 45549083112 scopus 로고    scopus 로고
    • Constitutive activation of signal transducers and activators of transcription predicts vorinostat resistance in cutaneous T-cell lymphoma
    • Fantin VR, Loboda A, Paweletz CP et al.: Constitutive activation of signal transducers and activators of transcription predicts vorinostat resistance in cutaneous T-cell lymphoma. Cancer Res. 68, 3785-3794 (2008).
    • (2008) Cancer Res. , vol.68 , pp. 3785-3794
    • Fantin, V.R.1    Loboda, A.2    Paweletz, C.P.3
  • 72
    • 71849117270 scopus 로고    scopus 로고
    • Potential effcacy of the oral histone deacetylase inhibitor vorinostat in a Phase i trial in follicular and mantle cell lymphoma
    • Watanabe T, Kato H, Kobayashi Y et al.: Potential effcacy of the oral histone deacetylase inhibitor vorinostat in a Phase I trial in follicular and mantle cell lymphoma. Cancer Sci. 101(1), 196-200 (2010).
    • (2010) Cancer Sci. , vol.101 , Issue.1 , pp. 196-200
    • Watanabe, T.1    Kato, H.2    Kobayashi, Y.3
  • 73
    • 77649133111 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in malignant pleural mesothelioma: Preclinical rationale and clinical trials
    • Paik PK, Krug LM: Histone deacetylase inhibitors in malignant pleural mesothelioma: preclinical rationale and clinical trials. J. Thorac. Oncol. 5, 275-279 (2010).
    • (2010) J. Thorac. Oncol. , vol.5 , pp. 275-279
    • Paik, P.K.1    Krug, L.M.2


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