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Volumn 4, Issue 2, 2005, Pages 83-85

Early clinical data and potential clinical utility of novel histone deacetylase inhibitors in prostate cancer

(1)  Reddy, G Kesava a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

17 ALLYLAMINO 17 DEMETHOXYGELDANAMYCIN; 2 MORPHOLINO 8 PHENYLCHROMONE; 3 PHENYLSULFAMOYLCINNAMOHYDROXAMIC ACID; 6 (2,6 DICHLOROPHENYL) 2 (4 FLUORO 3 METHYLANILINO) 8 METHYL 8H PYRIDO[2,3 D]PYRIMIDIN 7 ONE; ANTINEOPLASTIC AGENT; BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; BEVACIZUMAB; BORTEZOMIB; BUTYRIC ACID; DEPSIPEPTIDE; DEXAMETHASONE; DNA DEMETHYLATING AGENT; DOCETAXEL; EPOTHILONE B; ETOPOSIDE; FLAVOPIRIDOL; FLUDARABINE; GEMCITABINE; HISTONE DEACETYLASE INHIBITOR; IMATINIB; IMMUNOMODULATING AGENT; ISOTRETINOIN; LBH 589; N (2 AMINOPHENYL) 4 (3 PYRIDINYLMETHOXYCARBONYLAMINOMETHYL)BENZAMIDE; RETINOIC ACID; THALIDOMIDE DERIVATIVE; TRIBUTRIN; TUMOR NECROSIS FACTOR RELATED APOPTOSIS INDUCING LIGAND; UNCLASSIFIED DRUG; UNINDEXED DRUG; VALPROIC ACID; VORINOSTAT;

EID: 26944438280     PISSN: 15400352     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1540-0352(11)70115-9     Document Type: Article
Times cited : (2)

References (14)
  • 1
    • 13744264091 scopus 로고    scopus 로고
    • Epigenetic changes in prostate cancer: Implication for diagnosis and treatment
    • Li LC, Carroll PR, Dahiya R. Epigenetic changes in prostate cancer: implication for diagnosis and treatment. J Natl Cancer Inst 2005; 97:103-115.
    • (2005) J Natl Cancer Inst , vol.97 , pp. 103-115
    • Li, L.C.1    Carroll, P.R.2    Dahiya, R.3
  • 2
    • 0035755974 scopus 로고    scopus 로고
    • Histone deacetylases and cancer: Causes and therapies
    • Marks P, Rifkind RA, Richon VM, et al. Histone deacetylases and cancer: causes and therapies. Nat Rev Cancer 2001; 1:194-202.
    • (2001) Nat Rev Cancer , vol.1 , pp. 194-202
    • Marks, P.1    Rifkind, R.A.2    Richon, V.M.3
  • 3
    • 13844309711 scopus 로고    scopus 로고
    • Clinical development of histone deacetylase inhibitors as anticancer agents
    • Drummond DC, Noble CO, Kirpotin DB, et al. Clinical development of histone deacetylase inhibitors as anticancer agents. Annu Rev Pharmacol Toxicol 2005; 45:495-528.
    • (2005) Annu Rev Pharmacol Toxicol , vol.45 , pp. 495-528
    • Drummond, D.C.1    Noble, C.O.2    Kirpotin, D.B.3
  • 4
    • 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 Discov 2002; 1:287-99.
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 287-299
    • Johnstone, R.W.1
  • 5
  • 6
    • 0033551152 scopus 로고    scopus 로고
    • A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo and tumor activity against human tumors
    • Saito A, Yamashita T., Mariko Y, et al. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo and tumor activity against human tumors. Proc Natl Acad Sci USA 1999; 96:4592-4597.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 4592-4597
    • Saito, A.1    Yamashita, T.2    Mariko, Y.3
  • 7
    • 26944471480 scopus 로고    scopus 로고
    • Pharmacologic evaluations of MS-275 (NSC706995), a novel benzamide structure with a unique spectrum of antitumor activity
    • Abstract #4976
    • Sausville EA, Alley MC, Pacula-Cox CM et al: Pharmacologic evaluations of MS-275 (NSC706995), a novel benzamide structure with a unique spectrum of antitumor activity. Proc Am Assoc Cancer Res 2001; 42:927 (Abstract #4976)
    • (2001) Proc Am Assoc Cancer Res , vol.42 , pp. 927
    • Sausville, E.A.1    Alley, M.C.2    Pacula-Cox, C.M.3
  • 8
    • 21244458052 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma
    • Ryan QC, Headlee D, Acharya M, et al. Phase I and pharmacokinetic study of MS-275, a histone deacetylase inhibitor, in patients with advanced and refractory solid tumors or lymphoma. J Clin Oncol 2005; 23:3912-3922.
    • (2005) J Clin Oncol , vol.23 , pp. 3912-3922
    • Ryan, Q.C.1    Headlee, D.2    Acharya, M.3
  • 9
    • 85036802385 scopus 로고    scopus 로고
    • Phase I pharmacokinetic-pharmacodynamic trial of weekly MS-275, an oral histone deacetylase inhibitor
    • Abstract #3904
    • Donovan EA, Ryan Q, Acharya M, et al. Phase I pharmacokinetic- pharmacodynamic trial of weekly MS-275, an oral histone deacetylase inhibitor. J Clin Oncol 2005; 23(16 suppl):204s (Abstract #3904).
    • (2005) J Clin Oncol , vol.23 , Issue.16 SUPPL.
    • Donovan, E.A.1    Ryan, Q.2    Acharya, M.3
  • 10
    • 25144499136 scopus 로고    scopus 로고
    • Updated results from a phase I trial of the histone deacetylase (HDAC) inhibitor MS-275 in patients with refractory solid tumors
    • Abstract #3026
    • Gore L, Holden SN, Basche M, et al. Updated results from a phase I trial of the histone deacetylase (HDAC) inhibitor MS-275 in patients with refractory solid tumors. Proc Am Soc Clin Oncol 2004; 23:201 (Abstract #3026).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 201
    • Gore, L.1    Holden, S.N.2    Basche, M.3
  • 11
    • 0036828101 scopus 로고    scopus 로고
    • MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors
    • Jaboin J, Wild J, Hamidi H, et al. MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors. Cancer Res 2002; 62:6108-6115.
    • (2002) Cancer Res , vol.62 , pp. 6108-6115
    • Jaboin, J.1    Wild, J.2    Hamidi, H.3
  • 12
    • 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 2005; 23:3923-3931.
    • (2005) J Clin Oncol , vol.23 , pp. 3923-3931
    • Kelly, W.K.1    O'Connor, O.A.2    Krug, L.M.3
  • 13
    • 12444321545 scopus 로고    scopus 로고
    • Phase I clinical trial of histone deacetylase inhibitor: Suberoylanilide hydroxamic acid administered intravenously
    • Kelly WK, Richon VM, O'Connor O, et al. Phase I clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res 2003; 9:3578-3588.
    • (2003) Clin Cancer Res , vol.9 , pp. 3578-3588
    • Kelly, W.K.1    Richon, V.M.2    O'Connor, O.3
  • 14
    • 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 PTK787/ZK222584
    • Qian DZ, Wang X, Kachhap SK, et al. 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 PTK787/ZK222584. Cancer Res 2004; 64:6626-6634.
    • (2004) Cancer Res , vol.64 , pp. 6626-6634
    • Qian, D.Z.1    Wang, X.2    Kachhap, S.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.