Histone deacetylase inhibitors: Emerging anticancer therapeutic agents?

被引:20
作者
Kristeleit, Rebecca [1 ]
Fong, Peter [1 ]
Aherne, G. Wynne [1 ]
de Bono, Johann [1 ]
机构
[1] Royal Marsden Hosp, Inst Canc Res, Ctr Canc Therapeut, Sutton SM2 5PT, Surrey, England
关键词
acetylation; depsipeptide; nuclear factor-kappa B; retinoblastoma; suberoylanilide hydroxamic acid;
D O I
10.3816/CLC.2005.s.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Histone deacetylase inhibitors are novel anticancer agents in clinical development that target the family of histone deacetylase (HDAC) enzymes responsible for deacetylating core nucleosomal histories and other proteins. The precise mechanisms resulting in the antiproliferative biologic effects of these agents are not yet known, but there are several proposed mechanistic models, including transcriptional and nontranscriptional processes. Clinical experience with these agents indicates that they are generally well tolerated, and anticancer activity has been observed in early clinical trials in several tumor types including non-small-cell lung cancer. The development of these agents continues, with an emphasis on the discovery of HDAC isoform-selective compounds. Successful future development relies on clearer understanding of the dominant mechanisms involved in the observed anti proliferative effects.
引用
收藏
页码:S19 / S30
页数:12
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