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Volumn 8, Issue 2, 2005, Pages 144-154

Focus on deacetylation for therapeutic benefit

Author keywords

Apoptosis; Cancer clinical trials; Histone deacetylase; Histone deacetylase inhibitor; Mechanism; Preclinical; Re expression

Indexed keywords

3 CARBOXYCINNAMIC ACID BISHYDROXAMIDE; 3 PHENYLSULFAMOYLCINNAMOHYDROXAMIC ACID; 4 [N (2 HYDROXYETHYL) N [2 (3 INDOLYL)ETHYL]AMINOMETHYL]CINNAMOHYDROXAMIC ACID; 5 AZA 2' DEOXYCYTIDINE; ANTINEOPLASTIC AGENT; APICIDIN; ARYLBUTYRIC ACID DERIVATIVE; BUTYRIC ACID; CISPLATIN; DNA METHYLTRANSFERASE; DOXORUBICIN; ELLIPTICINE; ETOPOSIDE; FLAVOPIRIDOL; FLUOROURACIL; FR 901228; GYRASE INHIBITOR; HISTONE; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; IMATINIB; LBH 589A; METHYLTRANSFERASE INHIBITOR; N (2 AMINOPHENYL) 4 (3 PYRIDINYLMETHOXYCARBONYLAMINOMETHYL)BENZAMIDE; PHENYLACETIC ACID; PIVALOYLOXYMETHYL BUTYRATE; TRICHOSTATIN A; UNCLASSIFIED DRUG; UNINDEXED DRUG; VALPROIC ACID; VORINOSTAT;

EID: 14544277978     PISSN: 13697056     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (12)

References (129)
  • 1
    • 1842411320 scopus 로고    scopus 로고
    • Crystal structure of the nucleosome core particle at 2.8 Å resolution
    • Luger K, Mader AW, Richmond RK, Sargent DF, Richmond TJ: Crystal structure of the nucleosome core particle at 2.8 Å resolution. Nature (1997) 389(6648):251-260.
    • (1997) Nature , vol.389 , Issue.6648 , pp. 251-260
    • Luger, K.1    Mader, A.W.2    Richmond, R.K.3    Sargent, D.F.4    Richmond, T.J.5
  • 2
    • 0035986095 scopus 로고    scopus 로고
    • Dynamics of histone acetylation in vivo. A function for acetylation turnover?
    • Waterborg JH: Dynamics of histone acetylation in vivo A function for acetylation turnover? Biochem Cell Biol (2002) 80(3):363-378.
    • (2002) Biochem. Cell Biol. , vol.80 , Issue.3 , pp. 363-378
    • Waterborg, J.H.1
  • 3
    • 0141929385 scopus 로고    scopus 로고
    • Binary switches and modification cassettes in histone biology and beyond
    • Fischle W, Wang Y, Allis CD: Binary switches and modification cassettes in histone biology and beyond. Nature (2003) 425(6957):475-479.
    • (2003) Nature , vol.425 , Issue.6957 , pp. 475-479
    • Fischle, W.1    Wang, Y.2    Allis, C.D.3
  • 4
    • 0035862199 scopus 로고    scopus 로고
    • The human histone deacetylase family
    • Gray SG, Ekstrom TJ: The human histone deacetylase family. Exp Cell Res (2001) 262(2):75-83.
    • (2001) Exp. Cell Res. , vol.262 , Issue.2 , pp. 75-83
    • Gray, S.G.1    Ekstrom, T.J.2
  • 6
    • 0033609055 scopus 로고    scopus 로고
    • Three proteins define a class of human histone deacetylases related to yeast Hda1p
    • Grozinger CM, Hassig CA, Schreiber SL: Three proteins define a class of human histone deacetylases related to yeast Hda1p. Proc Natl Acad Sci USA (1999) 96(9):4868-4873.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , Issue.9 , pp. 4868-4873
    • Grozinger, C.M.1    Hassig, C.A.2    Schreiber, S.L.3
  • 7
    • 0037406061 scopus 로고    scopus 로고
    • Class II histone deacetylases: Versatile regulators
    • Verdin E, Dequiedt F, Kasler HG: Class II histone deacetylases: Versatile regulators. Trends Genet (2003) 19 5):286-293.
    • (2003) Trends Genet. , vol.19 , Issue.5 , pp. 286-293
    • Verdin, E.1    Dequiedt, F.2    Kasler, H.G.3
  • 8
    • 1842578986 scopus 로고    scopus 로고
    • Molecular evolution of the histone deacetylase family: Functional implications of phylogenetic analysis
    • Gregoretti IV, Lee YM, Goodson HV: Molecular evolution of the histone deacetylase family: Functional implications of phylogenetic analysis. J Mol Biol (2004) 338(1):17-31.
    • (2004) J. Mol. Biol. , vol.338 , Issue.1 , pp. 17-31
    • Gregoretti, I.V.1    Lee, Y.M.2    Goodson, H.V.3
  • 9
    • 0037123767 scopus 로고    scopus 로고
    • Microarray deacetylation maps determine genome-wide functions for yeast histone deacetylases
    • Robyr D, Suka Y, Xenarios I, Kurdistani SK, Wang A, Suka N, Grunstein M: Microarray deacetylation maps determine genome-wide functions for yeast histone deacetylases. Cell (2002) 109 4):437-446.
    • (2002) Cell , vol.109 , Issue.4 , pp. 437-446
    • Robyr, D.1    Suka, Y.2    Xenarios, I.3    Kurdistani, S.K.4    Wang, A.5    Suka, N.6    Grunstein, M.7
  • 10
    • 4544358659 scopus 로고    scopus 로고
    • Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development
    • Chang S, McKinsey TA, Zhang CL, Richardson JA, Hill JA, Olson EN: Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development. Mol Cell Biol (2004) 24(19):8467-8476.
    • (2004) Mol. Cell. Biol. , vol.24 , Issue.19 , pp. 8467-8476
    • Chang, S.1    McKinsey, T.A.2    Zhang, C.L.3    Richardson, J.A.4    Hill, J.A.5    Olson, E.N.6
  • 15
    • 0037306843 scopus 로고    scopus 로고
    • Quantification of histone acetyltransferase and histone deacetylase transcripts during early bovine embryo development
    • McGraw S, Robert C, Massicotte L, Sirard MA: Quantification of histone acetyltransferase and histone deacetylase transcripts during early bovine embryo development. Biol Reprod (2003) 68(2):383-389.
    • (2003) Biol. Reprod. , vol.68 , Issue.2 , pp. 383-389
    • McGraw, S.1    Robert, C.2    Massicotte, L.3    Sirard, M.A.4
  • 18
    • 2942731802 scopus 로고    scopus 로고
    • Dual roles of histone deacetylases in the control of cardiac growth
    • McKinsey TA, Olson EN: Dual roles of histone deacetylases in the control of cardiac growth. Novartis Foundation Symposium (2004) 259:132-141.
    • (2004) Novartis Foundation Symposium , vol.259 , pp. 132-141
    • McKinsey, T.A.1    Olson, E.N.2
  • 22
    • 0345357773 scopus 로고    scopus 로고
    • Gene silencing in cancer in association with promoter hypermethylation
    • Herman JG, Baylin SB: Gene silencing in cancer in association with promoter hypermethylation. N Engl J Med (2003) 349(21):2042-2054.
    • (2003) N. Engl. J. Med. , vol.349 , Issue.21 , pp. 2042-2054
    • Herman, J.G.1    Baylin, S.B.2
  • 23
    • 0036274359 scopus 로고    scopus 로고
    • The fundamental role of epigenetic events in cancer
    • Jones PA, Baylin SB: The fundamental role of epigenetic events in cancer. Nat Rev Genet (2002) 3(6):415-428.
    • (2002) Nat. Rev. Genet. , vol.3 , Issue.6 , pp. 415-428
    • Jones, P.A.1    Baylin, S.B.2
  • 24
    • 0036182132 scopus 로고    scopus 로고
    • Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation
    • El-Osta A, Kanthaddis P, Zalcberg JR, Wolffe AP: Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation. Mol Cell Biol (2002) 22(6):1844-1857.
    • (2002) Mol. Cell. Biol. , vol.22 , Issue.6 , pp. 1844-1857
    • El-Osta, A.1    Kanthaddis, P.2    Zalcberg, J.R.3    Wolffe, A.P.4
  • 26
    • 0017886958 scopus 로고
    • Sodium butyrate inhibits histone deacetylation in cultured cells
    • Candido EP, Reeves R, Davie JR: Sodium butyrate inhibits histone deacetylation in cultured cells. Cell (1978) 14 1):105-113.
    • (1978) Cell , vol.14 , Issue.1 , pp. 105-113
    • Candido, E.P.1    Reeves, R.2    Davie, J.R.3
  • 33
    • 0024996768 scopus 로고
    • Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by Trichostatin A
    • Yoshida M, Kijima M, Akita M, Beppu T: Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by Trichostatin A. J Biol Chem (1990) 265 28):17174-17179.
    • (1990) J. Biol. Chem. , vol.265 , Issue.28 , pp. 17174-17179
    • Yoshida, M.1    Kijima, M.2    Akita, M.3    Beppu, T.4
  • 34
    • 0034901985 scopus 로고    scopus 로고
    • Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo
    • Vigushin DM, Ali S, Pace PE, Mirsaidi N, Ito K, Adcock I, Coombes RC: Trichostatin A is a histone deacetylase inhibitor with potent antitumor activity against breast cancer in vivo. Clin Cancer Res (2001) 7(4):971-976.
    • (2001) Clin. Cancer Res. , vol.7 , Issue.4 , pp. 971-976
    • Vigushin, D.M.1    Ali, S.2    Pace, P.E.3    Mirsaidi, N.4    Ito, K.5    Adcock, I.6    Coombes, R.C.7
  • 36
    • 4344683925 scopus 로고    scopus 로고
    • Identification of genes upregulated by histone deacetylase inhibition with cDNA microarray and exploration of epigenetic alterations on hepatoma cells
    • Chiba T, Yokosuka O, Arai M, Tada M, Fukai K, Imazeki F, Kato M, Seki N, Saisho H: Identification of genes upregulated by histone deacetylase inhibition with cDNA microarray and exploration of epigenetic alterations on hepatoma cells. J Hepatol (2004) 41 3):436-445.
    • (2004) J. Hepatol. , vol.41 , Issue.3 , pp. 436-445
    • Chiba, T.1    Yokosuka, O.2    Arai, M.3    Tada, M.4    Fukai, K.5    Imazeki, F.6    Kato, M.7    Seki, N.8    Saisho, H.9
  • 41
    • 0344640906 scopus 로고    scopus 로고
    • Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation
    • Haggarty SJ, Koeller KM, Wong JC, Grozinger CM, Schreiber SL: Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation. Proc Natl Acad Sci USA (2003) 100(8):4389-4394.
    • (2003) Proc. Natl. Acad. Sci. USA , vol.100 , Issue.8 , pp. 4389-4394
    • Haggarty, S.J.1    Koeller, K.M.2    Wong, J.C.3    Grozinger, C.M.4    Schreiber, S.L.5
  • 45
    • 0042905956 scopus 로고    scopus 로고
    • Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: Defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
    • Glaser KB, Slaver MJ, Waring JF, Stender J, Ulrich RG, Davidsen SK: Gene expression profiling 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 (2003) 2 2):151-163.
    • (2003) Mol. Cancer Ther. , vol.2 , Issue.2 , pp. 151-163
    • Glaser, K.B.1    Slaver, M.J.2    Waring, J.F.3    Stender, J.4    Ulrich, R.G.5    Davidsen, S.K.6
  • 48
    • 0036527775 scopus 로고    scopus 로고
    • Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer
    • Johnstone RW: Histone-deacetylase inhibitors: Novel drugs for the treatment of cancer. Nat Rev Drug Disc (2002) 1 4):287-299.
    • (2002) Nat. Rev. Drug Disc. , vol.1 , Issue.4 , pp. 287-299
    • Johnstone, R.W.1
  • 50
    • 18644367141 scopus 로고    scopus 로고
    • Induction and superinduction of growth arrest and DNA damage gone 45 (GADD45) α and β messenger RNAs by histone deacetylase inhibitors trichostatin A (TSA) and butyrate in SW620 human colon carcinoma cells
    • Chen Z, Clark S, Birkeland M, Sung CM, Logo A, Liu R, Kirkpatrick R, Johanson K, Winkler JD, Hu E: Induction and superinduction of growth arrest and DNA damage gone 45 (GADD45) α and β messenger RNAs by histone deacetylase inhibitors trichostatin A (TSA) and butyrate in SW620 human colon carcinoma cells. Cancer Lett (2002) 188(1-2):127-140.
    • (2002) Cancer Lett. , vol.188 , Issue.1-2 , pp. 127-140
    • Chen, Z.1    Clark, S.2    Birkeland, M.3    Sung, C.M.4    Logo, A.5    Liu, R.6    Kirkpatrick, R.7    Johanson, K.8    Winkler, J.D.9    Hu, E.10
  • 51
    • 0344306402 scopus 로고    scopus 로고
    • Apoptotic pathways activated by histone deacetylase inhibitors: Implications for the drug-resistant phenotype
    • Henderson C, Brancolini C: Apoptotic pathways activated by histone deacetylase inhibitors: Implications for the drug-resistant phenotype. Drug Resistance Updates (2003) 6(5):247-256.
    • (2003) Drug Resistance Updates , vol.6 , Issue.5 , pp. 247-256
    • Henderson, C.1    Brancolini, C.2
  • 52
    • 0038485588 scopus 로고    scopus 로고
    • Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA)
    • Henderson C, Mizzau M, Paroni G, Maestro R, Schneider C, Brancolini C: Role of caspases, Bid, and p53 in the apoptotic response triggered by histone deacetylase inhibitors trichostatin-A (TSA) and suberoylanilide hydroxamic acid (SAHA). J Biol Chem (2003) 278(14):12579-12589.
    • (2003) J. Biol. Chem. , vol.278 , Issue.14 , pp. 12579-12589
    • Henderson, C.1    Mizzau, M.2    Paroni, G.3    Maestro, R.4    Schneider, C.5    Brancolini, C.6
  • 53
    • 0642345200 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor suberic bishydroxamate: A potential sensitizer of melanoma to TNF-related apoptosis-inducing ligand (TRAIL) induced apoptosis
    • Zhang XD, Gillespie SK, Borrow JM, Hersey P: The histone deacetylase inhibitor suberic bishydroxamate: A potential sensitizer of melanoma to TNF-related apoptosis-inducing ligand (TRAIL) induced apoptosis. Biochem Pharmacol (2003) 66(8):1537-1545.
    • (2003) Biochem. Pharmacol. , vol.66 , Issue.8 , pp. 1537-1545
    • Zhang, X.D.1    Gillespie, S.K.2    Borrow, J.M.3    Hersey, P.4
  • 54
    • 0038494686 scopus 로고    scopus 로고
    • Depsipeptide (FR-901228) induces histone acetylation and inhibition of histone deacetylase in chronic lymphocytic leukemia cells concurrent with activation of caspase 8-mediated apoptosis and down-regulation of c-FLIP protein
    • Aron JL, Parthun MR, Marcucci G, Kitada S, Mone AP, Davis ME, Shen T, Murphy T, Wickham J, Kanakry C, Lucas DM et al: Depsipeptide (FR-901228) induces histone acetylation and inhibition of histone deacetylase in chronic lymphocytic leukemia cells concurrent with activation of caspase 8-mediated apoptosis and down-regulation of c-FLIP protein. Blood (2003) 102(2):652-658.
    • (2003) Blood , vol.102 , Issue.2 , pp. 652-658
    • Aron, J.L.1    Parthun, M.R.2    Marcucci, G.3    Kitada, S.4    Mone, A.P.5    Davis, M.E.6    Shen, T.7    Murphy, T.8    Wickham, J.9    Kanakry, C.10    Lucas, D.M.11
  • 55
    • 4344716951 scopus 로고    scopus 로고
    • Modulation of pro- and anti-apoptotic factors in human melanoma cells exposed to histone deacetylase inhibitors
    • Facchetti F, Previdi S, Ballarini M, Minucci S, Perego P, Porta CA: Modulation of pro- and anti-apoptotic factors in human melanoma cells exposed to histone deacetylase inhibitors. Apoptosis (2004) 9(5):573-582.
    • (2004) Apoptosis , vol.9 , Issue.5 , pp. 573-582
    • Facchetti, F.1    Previdi, S.2    Ballarini, M.3    Minucci, S.4    Perego, P.5    Porta, C.A.6
  • 56
    • 0032989027 scopus 로고    scopus 로고
    • Antitumour activity in vitro and in vivo of selective differentiating agents containing hydroxamate
    • Qiu L, Kelso MJ, Hansen C, West ML, Fairlie DP, Parsons PG: Antitumour activity in vitro and in vivo of selective differentiating agents containing hydroxamate. Br J Cancer (1999) 80(8):1252-1258.
    • (1999) Br. J. Cancer , vol.80 , Issue.8 , pp. 1252-1258
    • Qiu, L.1    Kelso, M.J.2    Hansen, C.3    West, M.L.4    Fairlie, D.P.5    Parsons, P.G.6
  • 58
    • 4143070452 scopus 로고    scopus 로고
    • Redox modulation of chromatin remodeling: Impact on histone acetylation and deacetylation, NFκB and pro-inflammatory gene expression
    • Rahman I, Marwick J, Kirkham P: Redox modulation of chromatin remodeling: Impact on histone acetylation and deacetylation, NFκB and pro-inflammatory gene expression. Biochem Pharmacol (2004) 68(6):1255-1267.
    • (2004) Biochem. Pharmacol. , vol.68 , Issue.6 , pp. 1255-1267
    • Rahman, I.1    Marwick, J.2    Kirkham, P.3
  • 60
    • 0035845541 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species
    • Ruefli AA, Ausserlechner MJ, Bernhard D, Sutton VR, Tainton KM, Kofler R, Smyth MJ, Johnstone RW: The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species. Proc Natl Acad Sci USA (2001) 98(19):10833-10838.
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , Issue.19 , pp. 10833-10838
    • Ruefli, A.A.1    Ausserlechner, M.J.2    Bernhard, D.3    Sutton, V.R.4    Tainton, K.M.5    Kofler, R.6    Smyth, M.J.7    Johnstone, R.W.8
  • 61
    • 0035406174 scopus 로고    scopus 로고
    • WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937)
    • WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937). Int J Oncol (2001) 19(1):181-191.
    • (2001) Int. J. Oncol. , vol.19 , Issue.1 , pp. 181-191
    • Rosato, R.R.1    Wang, Z.2    Gopalkrishnan, R.V.3    Fisher, P.B.4    Grant, S.5
  • 65
    • 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, Amin S, Desai D, Pittman B, Richon VM: Suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, suppresses the growth of carcinogen-induced mammary tumors. Anticancer Res (2002) 22(3):1497-1504.
    • (2002) Anticancer Res. , vol.22 , Issue.3 , pp. 1497-1504
    • Cohen, L.A.1    Marks, P.A.2    Rifkind, R.A.3    Amin, S.4    Desai, D.5    Pittman, B.6    Richon, V.M.7
  • 67
    • 0037137896 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor FK-228 inhibits tumor angiogenesis
    • Kwon HJ, Kim MS, Kim W, Nakajima H, Kim KW: Histone deacetylase inhibitor FK-228 inhibits tumor angiogenesis. Int J Cancer (2002) 97(3):290-296.
    • (2002) Int. J. Cancer , vol.97 , Issue.3 , pp. 290-296
    • Kwon, H.J.1    Kim, M.S.2    Kim, W.3    Nakajima, H.4    Kim, K.W.5
  • 68
    • 4644364508 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor NVP-LAQ824 inhibits angiogenesis and has a greater antitumor effect in combination with the vascular endothelial growth factor receptor tyrosine kinase inhibitor PTK-787/ZK-222584
    • Qian DZ, Wang X, Kachhap SK, Kato Y, Wei Y, Zhang L, Atadja P, Pill R: The histone deacetylase inhibitor NVP-LAQ824 inhibits angiogenesis and has a greater antitumor effect in combination with the vascular endothelial growth factor receptor tyrosine kinase inhibitor PTK-787/ZK-222584. Cancer Res (2004) 64(18):6626-6634.
    • (2004) Cancer Res. , vol.64 , Issue.18 , pp. 6626-6634
    • Qian, D.Z.1    Wang, X.2    Kachhap, S.K.3    Kato, Y.4    Wei, Y.5    Zhang, L.6    Atadja, P.7    Pill, R.8
  • 69
    • 4143130097 scopus 로고    scopus 로고
    • A novel mechanism of chemoprotection by sulforaphane: Inhibition of histone deacetylase
    • Myzak MC, Karplus PA, Chung FL, Dashwood RH: A novel mechanism of chemoprotection by sulforaphane: Inhibition of histone deacetylase. Cancer Res (2004) 64(16):5767-5774.
    • (2004) Cancer Res. , vol.64 , Issue.16 , pp. 5767-5774
    • Myzak, M.C.1    Karplus, P.A.2    Chung, F.L.3    Dashwood, R.H.4
  • 75
    • 3643104150 scopus 로고    scopus 로고
    • Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase
    • Warrell RP Jr, He LZ, Richon V, Calleja E, Pandolfi PP: Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase. J Natl Cancer Inst (1998) 90(21):1621-1625.
    • (1998) J. Natl. Cancer Inst. , vol.90 , Issue.21 , pp. 1621-1625
    • Warrell Jr., R.P.1    He, L.Z.2    Richon, V.3    Calleja, E.4    Pandolfi, P.P.5
  • 76
    • 0034297220 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment
    • Huang L, Pardee AB: Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment. Mol Med (2000) 6(10):849-866.
    • (2000) Mol. Med. , vol.6 , Issue.10 , pp. 849-866
    • Huang, L.1    Pardee, A.B.2
  • 77
    • 0035866341 scopus 로고    scopus 로고
    • Combination of phenylbutyrate and 13-cis retinoic acid inhibits prostate tumor growth and angiogenesis
    • Pili R, Kruszewski MP, Hager BW, Lantz J, Carducci MA: Combination of phenylbutyrate and 13-cis retinoic acid inhibits prostate tumor growth and angiogenesis. Cancer Res (2001) 61 4):1477-1485.
    • (2001) Cancer Res. , vol.61 , Issue.4 , pp. 1477-1485
    • Pili, R.1    Kruszewski, M.P.2    Hager, B.W.3    Lantz, J.4    Carducci, M.A.5
  • 79
    • 0037642133 scopus 로고    scopus 로고
    • Deacetylase activity is required for recruitment of the basal transcription machinery and transactivation by STATS
    • Rascle A, Johnston JA, Amati B: Deacetylase activity is required for recruitment of the basal transcription machinery and transactivation by STATS. Mol Cell Biol (2003) 23 12):4162-4173.
    • (2003) Mol. Cell. Biol. , vol.23 , Issue.12 , pp. 4162-4173
    • Rascle, A.1    Johnston, J.A.2    Amati, B.3
  • 80
    • 0043016178 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor LAQ-824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells
    • Nimmanapalli R, Fuino L, Bali P, Gasparetto M, Glozak M, Tao J, Moscinski L, Smith C, Wu J, Jove R, Atadja P et al: Histone deacetylase inhibitor LAQ-824 both lowers expression and promotes proteasomal degradation of Bcr-Abl and induces apoptosis of imatinib mesylate-sensitive or -refractory chronic myelogenous leukemia-blast crisis cells. Cancer Res (2003) 63(16):5126-5135.
    • (2003) Cancer Res. , vol.63 , Issue.16 , pp. 5126-5135
    • Nimmanapalli, R.1    Fuino, L.2    Bali, P.3    Gasparetto, M.4    Glozak, M.5    Tao, J.6    Moscinski, L.7    Smith, C.8    Wu, J.9    Jove, R.10    Atadja, P.11
  • 81
    • 0038620379 scopus 로고    scopus 로고
    • Cotreatment with the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) enhances imatinib-induced apoptosis of Bcr-Abl-positive human acute leukemia cells
    • Nimmanapalli R, Fuino L, Stobaugh C, Richon V, Bhalla K: Cotreatment with the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) enhances imatinib-induced apoptosis of Bcr-Abl-positive human acute leukemia cells. Blood (2003) 101 8):3236-3239.
    • (2003) Blood , vol.101 , Issue.8 , pp. 3236-3239
    • Nimmanapalli, R.1    Fuino, L.2    Stobaugh, C.3    Richon, V.4    Bhalla, K.5
  • 84
    • 7944236356 scopus 로고    scopus 로고
    • Deacetylation of p53 after nerve growth factor treatment in PC12 cells as a post-translational modification mechanism of neurotrophin-induced tumor suppressor activation
    • Vaghefi H, Nest KE: Deacetylation of p53 after nerve growth factor treatment in PC12 cells as a post-translational modification mechanism of neurotrophin-induced tumor suppressor activation. Oncogene (2004) 23(49):8078-8087.
    • (2004) Oncogene , vol.23 , Issue.49 , pp. 8078-8087
    • Vaghefi, H.1    Nest, K.E.2
  • 85
    • 0036898253 scopus 로고    scopus 로고
    • Acetylation inactivates the transcriptional repressor Bcl-6
    • Bereshchenko OR, Ou W, Dalla-Favera R: Acetylation inactivates the transcriptional repressor Bcl-6. Nat Genet (2002) 32(4):606-613.
    • (2002) Nat. Genet. , vol.32 , Issue.4 , pp. 606-613
    • Bereshchenko, O.R.1    Ou, W.2    Dalla-Favera, R.3
  • 86
  • 88
    • 0036785378 scopus 로고    scopus 로고
    • Response to histone deacetylase inhibition of novel PML/RARα mutants detected in retinoic acid-resistant APL cells
    • Cote S, Rosenauer A, Bianchini A, Seiter K, Vandewiele J, Nervi C, Miller WH Jr: Response to histone deacetylase inhibition of novel PML/RARα mutants detected in retinoic acid-resistant APL cells. Blood (2002) 100(7):2586-2596.
    • (2002) Blood , vol.100 , Issue.7 , pp. 2586-2596
    • Cote, S.1    Rosenauer, A.2    Bianchini, A.3    Seiter, K.4    Vandewiele, J.5    Nervi, C.6    Miller Jr., W.H.7
  • 89
    • 0035328528 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid
    • Coffey DC, Kutko MC, Glick RD, Butler LM, Heller G, Rifkind RA, Marks PA, Richon VM, La Quaglia MP: The histone deacetylase inhibitor, CBHA, inhibits growth of human neuroblastoma xenografts in vivo, alone and synergistically with all-trans retinoic acid. Cancer Res (2001) 61(9):3591-3594.
    • (2001) Cancer Res. , vol.61 , Issue.9 , pp. 3591-3594
    • Coffey, D.C.1    Kutko, M.C.2    Glick, R.D.3    Butler, L.M.4    Heller, G.5    Rifkind, R.A.6    Marks, P.A.7    Richon, V.M.8    La Quaglia, M.P.9
  • 90
    • 0035835483 scopus 로고    scopus 로고
    • Effects of retinoic acid and sodium butyrate on gene expression, histone acetylation and inhibition of proliferation of melanoma cells
    • Demary K, Wong L, Spanjaard RA: Effects of retinoic acid and sodium butyrate on gene expression, histone acetylation and inhibition of proliferation of melanoma cells. Cancer Lett (2001) 163(1):103-107.
    • (2001) Cancer Lett. , vol.163 , Issue.1 , pp. 103-107
    • Demary, K.1    Wong, L.2    Spanjaard, R.A.3
  • 92
    • 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, Myohanen S, Herman JG, Baylin SB: Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer. Nat Genet (1999) 21(1):103-107.
    • (1999) Nat. Genet. , vol.21 , Issue.1 , pp. 103-107
    • Cameron, E.E.1    Bachman, K.E.2    Myohanen, S.3    Herman, J.G.4    Baylin, S.B.5
  • 93
    • 0036746906 scopus 로고    scopus 로고
    • Antineoplastic action of 5-aza-2′-deoxycytidine and phenylbutyrate on human lung carcinoma cells
    • Boivin AJ, Momparler LF, Hurtubise A, Momparler RL: Antineoplastic action of 5-aza-2′-deoxycytidine and phenylbutyrate on human lung carcinoma cells. Anticancer Drugs (2002) 13 8):869-874.
    • (2002) Anticancer Drugs , vol.13 , Issue.8 , pp. 869-874
    • Boivin, A.J.1    Momparler, L.F.2    Hurtubise, A.3    Momparler, R.L.4
  • 94
    • 0037276902 scopus 로고    scopus 로고
    • The interaction of histone deacetylase inhibitors and DNA methyltransferase inhibitors in the treatment of human cancer cells
    • Zhu WG, Otterson GA: The interaction of histone deacetylase inhibitors and DNA methyltransferase inhibitors in the treatment of human cancer cells. Curr Med Chem Anticancer Agents (2003) 3(3):187-199.
    • (2003) Curr. Med. Chem. Anticancer Agents , vol.3 , Issue.3 , pp. 187-199
    • Zhu, W.G.1    Otterson, G.A.2
  • 95
    • 0242330341 scopus 로고    scopus 로고
    • A novel histone deacetylase inhibitor, scriptaid, enhances expression of functional estrogen receptor α (ER) in ER negative human breast cancer cells in combination with 5-aza 2′-deoxycytidine
    • Keen JC, Yan L, Mack KM, Pettit C, Smith D, Sharma D, Davidson NE: A novel histone deacetylase inhibitor, scriptaid, enhances expression of functional estrogen receptor α (ER) in ER negative human breast cancer cells in combination with 5-aza 2′-deoxycytidine. Breast Cancer Res Treat (2003) 81 3):177-186.
    • (2003) Breast Cancer Res. Treat. , vol.81 , Issue.3 , pp. 177-186
    • Keen, J.C.1    Yan, L.2    Mack, K.M.3    Pettit, C.4    Smith, D.5    Sharma, D.6    Davidson, N.E.7
  • 97
    • 0037358032 scopus 로고    scopus 로고
    • Interaction of 5-aze-2′-deoxycytidine and depsipeptide on antineoplastic activity and activation of 14-3-3σ, E-cadherin and tissue inhibitor of metalloproteinase 3 expression in human breast carcinoma cells
    • Gagnon J, Shaker S, Primeau M, Hurtubise A, Momparler RL: Interaction of 5-aze-2′-deoxycytidine and depsipeptide on antineoplastic activity and activation of 14-3-3σ, E-cadherin and tissue inhibitor of metalloproteinase 3 expression in human breast carcinoma cells. Anticancer Drugs (2003) 14(3):193-202.
    • (2003) Anticancer Drugs , vol.14 , Issue.3 , pp. 193-202
    • Gagnon, J.1    Shaker, S.2    Primeau, M.3    Hurtubise, A.4    Momparler, R.L.5
  • 98
    • 0037328501 scopus 로고    scopus 로고
    • Depsipeptide (FR-901228) promotes histone acetylation, gene transcription, apoptosis and its activity is enhanced by DNA methyltransferase inhibitors in AML1/ETO-positive leukemic cells
    • Klisovic MI, Maghraby EA, Parthun MR, Gulmond M, Sklenar AR, Whitman SP, Chan KK, Murphy T, Anon J, Archer KJ, Rush LJ et al: Depsipeptide (FR-901228) promotes histone acetylation, gene transcription, apoptosis and its activity is enhanced by DNA methyltransferase inhibitors in AML1/ETO-positive leukemic cells. Leukemia (2003) 17(2):350-358.
    • (2003) Leukemia , vol.17 , Issue.2 , pp. 350-358
    • Klisovic, M.I.1    Maghraby, E.A.2    Parthun, M.R.3    Gulmond, M.4    Sklenar, A.R.5    Whitman, S.P.6    Chan, K.K.7    Murphy, T.8    Anon, J.9    Archer, K.J.10    Rush, L.J.11
  • 99
    • 0037427805 scopus 로고    scopus 로고
    • Synergistic antineoplastic action of DNA methylation inhibitor 5-aza-2′-deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells
    • Primeau M, Gagnon J, Momparler RL: Synergistic antineoplastic action of DNA methylation inhibitor 5-aza-2′-deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells. Int J Cancer (2003) 103 2):177-184.
    • (2003) Int. J. Cancer , vol.103 , Issue.2 , pp. 177-184
    • Primeau, M.1    Gagnon, J.2    Momparler, R.L.3
  • 101
    • 1342308338 scopus 로고    scopus 로고
    • WAF1/CIP1 down-regulation in synergistic antileukemic interactions between the histone deacetylase inhibitor sodium butyrate and flavopiridol
    • WAF1/CIP1 down-regulation in synergistic antileukemic interactions between the histone deacetylase inhibitor sodium butyrate and flavopiridol. Mol Pharmacol (2004) 65 3):571-581.
    • (2004) Mol. Pharmacol. , vol.65 , Issue.3 , pp. 571-581
    • Rosato, R.R.1    Almenara, J.A.2    Yu, C.3    Grant, S.4
  • 102
    • 0036050151 scopus 로고    scopus 로고
    • Synergistic induction of mitochondrial damage and apoptosis in human leukemia cells by flavopiridol and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA)
    • Almenara J, Rosato R, Grant S: Synergistic induction of mitochondrial damage and apoptosis in human leukemia cells by flavopiridol and the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA). Leukemia (2002) 16(7):1331-1343.
    • (2002) Leukemia , vol.16 , Issue.7 , pp. 1331-1343
    • Almenara, J.1    Rosato, R.2    Grant, S.3
  • 103
    • 1842481018 scopus 로고    scopus 로고
    • Abrogation of p21 expression by flavopiridol enhances depsipeptide-mediated apoptosis in malignant pleural mesothelioma cells
    • Nguyen DM, Schrump WD, Chen GA, Tsai W, Nguyen P, Trepel JB, Schrump DS: Abrogation of p21 expression by flavopiridol enhances depsipeptide-mediated apoptosis in malignant pleural mesothelioma cells. Clin Cancer Res (2004) 10(5):1813-1825.
    • (2004) Clin. Cancer Res. , vol.10 , Issue.5 , pp. 1813-1825
    • Nguyen, D.M.1    Schrump, W.D.2    Chen, G.A.3    Tsai, W.4    Nguyen, P.5    Trepel, J.B.6    Schrump, D.S.7
  • 104
    • 0038066488 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors promote STI-571-mediated apoptosis in STI-571-sensitive and - Resistant Bcr/Abl+ human myeloid leukemia cells
    • Yu C, Rahmani M, Almenara J, Subler M, Krystal G, Conrad D, Varticovskii L, Dent P, Grant S: Histone deacetylase inhibitors promote STI-571-mediated apoptosis in STI-571-sensitive and - resistant Bcr/Abl+ human myeloid leukemia cells. Cancer Res (2003) 63 9):2118-2126.
    • (2003) Cancer Res. , vol.63 , Issue.9 , pp. 2118-2126
    • Yu, C.1    Rahmani, M.2    Almenara, J.3    Subler, M.4    Krystal, G.5    Conrad, D.6    Varticovskii, L.7    Dent, P.8    Grant, S.9
  • 105
    • 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 STI-571
    • 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 STI-571. Blood (2003) 102(10):3765-3774.
    • (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
  • 106
    • 1642580501 scopus 로고    scopus 로고
    • Apicidin potentiates the imatinib-induced apoptosis of Bcr-Abl-positive human leukaemia cells by enhancing the activation of mitochondria-dependent caspase cascades
    • Kim JS, Jeung HK, Cheong JW, Maeng H, Lee ST, Hahn JS, Ko YW, Min YH: Apicidin potentiates the imatinib-induced apoptosis of Bcr-Abl-positive human leukaemia cells by enhancing the activation of mitochondria-dependent caspase cascades. Br J Haematol (2004) 124(2):166-178.
    • (2004) Br. J. Haematol. , vol.124 , Issue.2 , pp. 166-178
    • Kim, J.S.1    Jeung, H.K.2    Cheong, J.W.3    Maeng, H.4    Lee, S.T.5    Hahn, J.S.6    Ko, Y.W.7    Min, Y.H.8
  • 107
    • 0035552571 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor sodium butyrate induces DNA topoisomerase II α expression and confers hypersensitivity to etoposide in human leukemic cell lines
    • Kurz EU, Wilson SE, Leader KB, Sampey BP, Allan WP, Yalowich JC, Kroll DJ: The histone deacetylase inhibitor sodium butyrate induces DNA topoisomerase II α expression and confers hypersensitivity to etoposide in human leukemic cell lines. Mol Cancer Ther (2001) 1(2):121-131.
    • (2001) Mol. Cancer Ther. , vol.1 , Issue.2 , pp. 121-131
    • Kurz, E.U.1    Wilson, S.E.2    Leader, K.B.3    Sampey, B.P.4    Allan, W.P.5    Yalowich, J.C.6    Kroll, D.J.7
  • 108
    • 84895203376 scopus 로고    scopus 로고
    • A combination of histone deacetylase inhibitor LBH-589 and the Hsp90 inhibitor 17-AAG is highly active against human CML-BC and AML cells with constitutively active mutant Flt-3 tyrosine kinase
    • Abs 6541
    • Bhalla K, George P, Gutti R, Bali P, Tao J, Guo F, Sigua C, Li Y, Cohen P, Atadja P: A combination of histone deacetylase inhibitor LBH-589 and the Hsp90 inhibitor 17-AAG is highly active against human CML-BC and AML cells with constitutively active mutant Flt-3 tyrosine kinase. Proc Am Soc Clin Oncol (2004) 23:Abs 6541.
    • (2004) Proc. Am. Soc. Clin. Oncol. , vol.23
    • Bhalla, K.1    George, P.2    Gutti, R.3    Bali, P.4    Tao, J.5    Guo, F.6    Sigua, C.7    Li, Y.8    Cohen, P.9    Atadja, P.10
  • 109
    • 0345734267 scopus 로고    scopus 로고
    • Coadministration of the heat shock protein 90 antagonist 17-allylamino-17-demethoxygeldanamycin with suberoylanilide hydroxamic acid or sodium butyrate synergistically induces apoptosis in human leukemia cells
    • Rahmani M, Yu C, Dai Y, Reese E, Ahmed W, Dent P, Grant S: Coadministration of the heat shock protein 90 antagonist 17-allylamino-17-demethoxygeldanamycin with suberoylanilide hydroxamic acid or sodium butyrate synergistically induces apoptosis in human leukemia cells. Cancer Res (2003) 63(23):8420-8427.
    • (2003) Cancer Res. , vol.63 , Issue.23 , pp. 8420-8427
    • Rahmani, M.1    Yu, C.2    Dai, Y.3    Reese, E.4    Ahmed, W.5    Dent, P.6    Grant, S.7
  • 110
    • 0242610850 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA
    • Kim MS, Blake M, Bask JH, Kohlhagen G, Pommier Y, Carrier F: Inhibition of histone deacetylase increases cytotoxicity to anticancer drugs targeting DNA. Cancer Res (2003) 63(21):7291-7300.
    • (2003) Cancer Res. , vol.63 , Issue.21 , pp. 7291-7300
    • Kim, M.S.1    Blake, M.2    Bask, J.H.3    Kohlhagen, G.4    Pommier, Y.5    Carrier, F.6
  • 111
    • 0034769471 scopus 로고    scopus 로고
    • Chemical agents that promote chromatin compaction radiosensitize tumour cells
    • Biade S, Stobbe CC, Boyd JT, Chapman JD: Chemical agents that promote chromatin compaction radiosensitize tumour cells. Int J Radiat Biol (2001) 77(10):1033-1042.
    • (2001) Int. J. Radiat. Biol. , vol.77 , Issue.10 , pp. 1033-1042
    • Biade, S.1    Stobbe, C.C.2    Boyd, J.T.3    Chapman, J.D.4
  • 112
    • 1642576220 scopus 로고    scopus 로고
    • Enhanced radiation-induced cell killing and prolongation of γH2AX foci expression by the histone deacetylase inhibitor MS-275
    • Camphausen K, Burgan W, Cerra M, Oswald KA, Trepell JB, Lee MJ, Tofilon PJ: Enhanced radiation-induced cell killing and prolongation of γH2AX foci expression by the histone deacetylase inhibitor MS-275. Cancer Res (2004) 64(1):316-321.
    • (2004) Cancer Res. , vol.64 , Issue.1 , pp. 316-321
    • Camphausen, K.1    Burgan, W.2    Cerra, M.3    Oswald, K.A.4    Trepell, J.B.5    Lee, M.J.6    Tofilon, P.J.7
  • 113
    • 4644259264 scopus 로고    scopus 로고
    • Enhancement of xenograft tumor radiosensitivity by the histone deacetylase inhibitor MS-275 and correlation with histone hyperacetylation
    • Camphausen K, Scott T, Sproull M, Tofilon PJ: Enhancement of xenograft tumor radiosensitivity by the histone deacetylase inhibitor MS-275 and correlation with histone hyperacetylation. Clin Cancer Res (2004) 10(18 Pt 1):6066-6071.
    • (2004) Clin. Cancer Res. , vol.10 , Issue.18 PART 1 , pp. 6066-6071
    • Camphausen, K.1    Scott, T.2    Sproull, M.3    Tofilon, P.J.4
  • 114
    • 3042568739 scopus 로고    scopus 로고
    • Susceptibility and radiosensitization of human glioblastoma cells to trichostatin A, a histone deacetylase inhibitor
    • Kim JH, Shin JH, Kim IH: Susceptibility and radiosensitization of human glioblastoma cells to trichostatin A, a histone deacetylase inhibitor. Int J Radiat Oncol Biol Phys (2004) 59(4):1174-1180.
    • (2004) Int. J. Radiat. Oncol. Biol. Phys. , vol.59 , Issue.4 , pp. 1174-1180
    • Kim, J.H.1    Shin, J.H.2    Kim, I.H.3
  • 115
    • 2342564962 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors FK-228, N-(2-aminophenyl)-4-N-(pyridin-3-yl-methoxycarbonyl)amino- methyl]benzamide and m-carboxy-cinnamic acid bis-hydroxamide augment radiation-induced cell death in gastrointestinal adenocarcinoma cells
    • Zhang Y, Adachi M, Zhao X, Kawamura R, Imai K: Histone deacetylase inhibitors FK-228, N-(2-aminophenyl)-4-N (pyridin-3-yl-methoxycarbonyl)amino-methyl]benzamide and m-carboxy-cinnamic acid bis-hydroxamide augment radiation-induced cell death in gastrointestinal adenocarcinoma cells. Int J Cancer (2004) 110(2):301-308.
    • (2004) Int. J. Cancer , vol.110 , Issue.2 , pp. 301-308
    • Zhang, Y.1    Adachi, M.2    Zhao, X.3    Kawamura, R.4    Imai, K.5
  • 116
    • 0034908231 scopus 로고    scopus 로고
    • Evers BM: Butyrate sensitizes human colon cancer cells to TRAIL-mediated apoptosis
    • Hernandez A, Thomas R, Smith F, Sandberg J, Kim S, Chung DH, Evers BM: Butyrate sensitizes human colon cancer cells to TRAIL-mediated apoptosis. Surgery (2001) 130(2):265-272.
    • (2001) Surgery , vol.130 , Issue.2 , pp. 265-272
    • Hernandez, A.1    Thomas, R.2    Smith, F.3    Sandberg, J.4    Kim, S.5    Chung, D.H.6
  • 117
    • 0036584375 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors sensitize human colonic adenocarcinoma cell lines to TNF-related apoptosis inducing ligand-mediated apoptosis
    • Inoue H, Shiraki K, Ohmod S, Sakai T, Deguchi M, Yamanaka T, Okano H, Nakano T: Histone deacetylase inhibitors sensitize human colonic adenocarcinoma cell lines to TNF-related apoptosis inducing ligand-mediated apoptosis. Int J Mol Med (2002) 9 5):521-525.
    • (2002) Int. J. Mol. Med. , vol.9 , Issue.5 , pp. 521-525
    • Inoue, H.1    Shiraki, K.2    Ohmod, S.3    Sakai, T.4    Deguchi, M.5    Yamanaka, T.6    Okano, H.7    Nakano, T.8
  • 118
    • 2942584501 scopus 로고    scopus 로고
    • Simultaneous activation of the intrinsic and extrinsic pathways by histone deacetylase (HDAC) inhibitors and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) synergistically induces mitochondrial damage and apoptosis in human leukemia cells
    • Rosato RR, Almenara JA, Dai Y, Grant S: Simultaneous activation of the intrinsic and extrinsic pathways by histone deacetylase (HDAC) inhibitors and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) synergistically induces mitochondrial damage and apoptosis in human leukemia cells. Mol Cancer Ther (2003) 2 12):1273-1284.
    • (2003) Mol. Cancer Ther. , vol.2 , Issue.12 , pp. 1273-1284
    • Rosato, R.R.1    Almenara, J.A.2    Dai, Y.3    Grant, S.4
  • 120
    • 13844261436 scopus 로고    scopus 로고
    • Update on the phase II trial and correlative studies of depsipeptide in patients with cutaneous T-cell lymphoma and relapsed peripheral T-cell lymphoma
    • Abs 3028
    • Piekarz R, Frye R, Turner BM, Wright J, Leonard J, Allen S, Bates S: Update on the phase II trial and correlative studies of depsipeptide in patients with cutaneous T-cell lymphoma and relapsed peripheral T-cell lymphoma. Proc Am Soc Clin Oncol (2004) 23 Abs 3028.
    • (2004) Proc. Am. Soc. Clin. Oncol. , vol.23
    • Piekarz, R.1    Frye, R.2    Turner, B.M.3    Wright, J.4    Leonard, J.5    Allen, S.6    Bates, S.7
  • 121
    • 0009759670 scopus 로고    scopus 로고
    • Pivanex activity in refractory nonsmall cell lung cancer, a phase II study
    • Abs 1253
    • Keer H, Raid T, Sreedharan S: Pivanex activity in refractory nonsmall cell lung cancer, a phase II study. Proc Am Soc Clin Oncol (2002) 21:Abs 1253.
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Keer, H.1    Raid, T.2    Sreedharan, S.3
  • 124
    • 0034885248 scopus 로고    scopus 로고
    • A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies
    • Gilbert J, Baker SD, Bowling MK, Grochow L, Figg WD, Zabelina Y, Donehower RC, Carducci MA: A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies. Clin Cancer Res (2001) 7 8):2292-2300.
    • (2001) Clin. Cancer Res. , vol.7 , Issue.8 , pp. 2292-2300
    • Gilbert, J.1    Baker, S.D.2    Bowling, M.K.3    Grochow, L.4    Figg, W.D.5    Zabelina, Y.6    Donehower, R.C.7    Carducci, M.A.8
  • 125
    • 79957865372 scopus 로고    scopus 로고
    • Methyltransferase (MT) activity and gene expression in tumor biopsies from patients enrolled in a phase I study of the MT inhibitor, 5-azacytidine (5AC), and the histone deacetylase inhibitor, phenylbutyrate (PB), in refractory solid tumors
    • Abs 343
    • Gilbert J, Baker SD, Donehower RC, Herman JG, DeMarzo A, Carducci M: Methyltransferase (MT) activity and gene expression in tumor biopsies from patients enrolled in a phase I study of the MT inhibitor, 5-azacytidine (5AC), and the histone deacetylase inhibitor, phenylbutyrate (PB), in refractory solid tumors. Proc Am Soc Clin Oncol (2001) 20(87a):Abs 343.
    • (2001) Proc. Am. Soc. Clin. Oncol. , vol.20 , Issue.87 a
    • Gilbert, J.1    Baker, S.D.2    Donehower, R.C.3    Herman, J.G.4    DeMarzo, A.5    Carducci, M.6
  • 128
    • 34248663408 scopus 로고    scopus 로고
    • Effects of the histone deacetylase inhibitor (HDACI) LAQ-824 on histone acetylation, Hsp70 and c-Raf in peripheral blood lymphocytes from patients with advanced solid tumours enrolled in a phase I clinical trial
    • Abs 3023
    • Kristeleit RS, Tandy D, Atadja P, Patnaik A, Scott J, DeBono JS, Judson I, Kaye SB, Workman P, Aherne W: Effects of the histone deacetylase inhibitor (HDACI) LAQ-824 on histone acetylation, Hsp70 and c-Raf in peripheral blood lymphocytes from patients with advanced solid tumours enrolled in a phase I clinical trial. Proc Am Soc Clin Oncol (2004) 23:Abs 3023.
    • (2004) Proc. Am. Soc. Clin. Oncol. , vol.23
    • Kristeleit, R.S.1    Tandy, D.2    Atadja, P.3    Patnaik, A.4    Scott, J.5    DeBono, J.S.6    Judson, I.7    Kaye, S.B.8    Workman, P.9    Aherne, W.10


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