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用于抗癌的表观遗传药物:从化学到癌症治疗,前路漫漫。

Epi-drugs to fight cancer: from chemistry to cancer treatment, the road ahead.

作者信息

Mai Antonello, Altucci Lucia

机构信息

Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza Università di Roma, 00185 Roma, IT, Italy.

出版信息

Int J Biochem Cell Biol. 2009 Jan;41(1):199-213. doi: 10.1016/j.biocel.2008.08.020. Epub 2008 Aug 22.

Abstract

In addition to genetic events, a variety of epigenetic events have been widely reported to contribute to the onset of many diseases including cancer. DNA methylation and histone modifications (such as acetylation, methylation, sumoylation, and phosphorylation) involving chromatin remodelling are among the most studied epigenetic mechanisms for regulation of gene expression leading, when altered, to some diseases. Epigenetic therapy tries to reverse the aberrations followed to the disruption of the balance of the epigenetic signalling ways through the use of both natural compounds and synthetic molecules, active on specific epi-targets. Such epi-drugs are, for example, inhibitors of DNA methyltransferases, histone deacetylases, histone acetyltransferases, histone methyltransferases, and histone demethylases. In this review we will focus on the chemical aspects of such molecules, joined to their effective (or potential) application in cancer therapy.

摘要

除了基因事件外,多种表观遗传事件也被广泛报道与包括癌症在内的许多疾病的发生有关。涉及染色质重塑的DNA甲基化和组蛋白修饰(如乙酰化、甲基化、SUMO化和磷酸化)是调控基因表达时研究最多的表观遗传机制,当这些机制发生改变时会导致一些疾病。表观遗传疗法试图通过使用对特定表观靶点有活性的天然化合物和合成分子来逆转表观遗传信号通路平衡被破坏后出现的异常。这类表观遗传药物例如有DNA甲基转移酶抑制剂、组蛋白去乙酰化酶抑制剂、组蛋白乙酰转移酶抑制剂、组蛋白甲基转移酶抑制剂和组蛋白去甲基化酶抑制剂。在本综述中,我们将重点关注这类分子的化学方面,以及它们在癌症治疗中的有效(或潜在)应用。

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