School of Chemistry, University of Southampton, Southampton, SO17 1BJ, UK.
Curr Cancer Drug Targets. 2009 Dec;9(8):963-81. doi: 10.2174/156800909790192428.
Histone proteins are subject to a diverse range of post-translational modifications which, along with DNA methylation, play a major role in controlling gene expression, cell division, survival and differentiation. Alterations in these chromatin modifications are thought to contribute to important human diseases including cancer. Inhibition of the enzymes that introduce and remove these chromatin modifications is proving an effective approach to cancer therapy and inhibitors of histone deacetylases and DNA methyltransferases have been approved for use in haematological malignancies. Here we provide a background to the biology of chromatin modifications and review some of the evidence validating histone deacetylases and DNA methyltransferases as targets for anti-cancer drug discovery. We then focus on two of the key issues in this field; the identification of novel inhibitors to overcome shortcomings of first generation agents and the potential role of histone deacetylase and DNA methyltransferase inhibitors in combination therapies for oncology. Finally, we highlight some of the challenges that will need to addressed to further progress the development of epigenetic-based therapies for cancer.
组蛋白蛋白质会受到多种翻译后修饰的影响,这些修饰连同 DNA 甲基化一起,在控制基因表达、细胞分裂、存活和分化方面发挥着重要作用。这些染色质修饰的改变被认为是导致包括癌症在内的重要人类疾病的原因之一。抑制引入和去除这些染色质修饰的酶已被证明是癌症治疗的一种有效方法,组蛋白去乙酰化酶和 DNA 甲基转移酶的抑制剂已被批准用于血液恶性肿瘤。在这里,我们提供了染色质修饰生物学的背景知识,并回顾了一些将组蛋白去乙酰化酶和 DNA 甲基转移酶确认为抗癌药物发现靶点的证据。然后,我们将重点关注该领域的两个关键问题:确定新型抑制剂以克服第一代药物的缺点,以及组蛋白去乙酰化酶和 DNA 甲基转移酶抑制剂在肿瘤联合治疗中的潜在作用。最后,我们强调了为癌症开发基于表观遗传的治疗方法需要解决的一些挑战。