Acharya Milin R, Sparreboom Alex, Venitz Jürgen, Figg William D
Clinical Pharmacology Research Core, National Cancer Institute, Bethesda, MD 20892, USA.
Mol Pharmacol. 2005 Oct;68(4):917-32. doi: 10.1124/mol.105.014167. Epub 2005 Jun 14.
The epigenome is defined by DNA methylation patterns and the associated post-translational modifications of histones. This histone code determines the expression status of individual genes dependent upon their localization on the chromatin. The histone deacetylases (HDACs) play a major role in keeping the balance between the acetylated and deacetylated states of chromatin and eventually regulate gene expression. Recent developments in understanding the cancer cell cycle, specifically the interplay with chromatin control, are providing opportunities for developing mechanism-based therapeutic drugs. Inhibitors of HDACs are under considerable exploration, in part because of their potential roles in reversing the silenced genes in transformed tumor cells by modulating transcriptional processes. This review is an effort to summarize the nonclinical and clinical status of HDAC inhibitors currently under development in anticancer therapy.
表观基因组由DNA甲基化模式以及相关的组蛋白翻译后修饰所定义。这种组蛋白密码决定了各个基因的表达状态,这取决于它们在染色质上的定位。组蛋白去乙酰化酶(HDACs)在维持染色质乙酰化和去乙酰化状态之间的平衡并最终调节基因表达方面发挥着主要作用。在理解癌细胞周期方面的最新进展,特别是与染色质控制的相互作用,为开发基于机制的治疗药物提供了机会。HDAC抑制剂正在进行大量研究,部分原因是它们通过调节转录过程在逆转转化肿瘤细胞中沉默基因方面的潜在作用。这篇综述旨在总结目前正在开发用于抗癌治疗的HDAC抑制剂的非临床和临床状况。