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组蛋白去乙酰化酶抑制剂介导的癌细胞毒性:作用机制及潜在临床意义

Cytotoxicity mediated by histone deacetylase inhibitors in cancer cells: mechanisms and potential clinical implications.

作者信息

Schrump David S

机构信息

Thoracic Oncology Section, Surgery Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892-1201, USA.

出版信息

Clin Cancer Res. 2009 Jun 15;15(12):3947-57. doi: 10.1158/1078-0432.CCR-08-2787. Epub 2009 Jun 9.

Abstract

Aberrant expression of epigenetic regulators of gene expression contributes to initiation and progression of cancer. During recent years, considerable research efforts have focused on the role of histone acetyltransferases (HATs) and histone deacetylases (HDACs) in cancer cells, and the identification of pharmacologic agents that modulate gene expression via inhibition of HDACs. The following review highlights recent studies pertaining to HDAC expression in cancer cells, the plieotropic mechanisms by which HDAC inhibitors (HDACi) mediate antitumor activity, and the potential clinical implications of HDAC inhibition as a strategy for cancer therapy.

摘要

基因表达的表观遗传调控因子的异常表达促进了癌症的发生和发展。近年来,大量研究工作聚焦于组蛋白乙酰转移酶(HATs)和组蛋白去乙酰化酶(HDACs)在癌细胞中的作用,以及通过抑制HDACs来调节基因表达的药物制剂的鉴定。以下综述重点介绍了有关癌细胞中HDAC表达的最新研究、HDAC抑制剂(HDACi)介导抗肿瘤活性的多效性机制,以及HDAC抑制作为癌症治疗策略的潜在临床意义。

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