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靶向组蛋白甲基转移酶的癌症药物发现:最新进展

Cancer drug discovery targeting histone methyltransferases: an update.

作者信息

Zhao Hongyu, Wang Ying, Li Huanqiu

机构信息

Research and Development, AbbVie Inc. 1 North Waukegan Road, North Chicago, IL60064, USA.

出版信息

Curr Med Chem. 2015;22(17):2075-86. doi: 10.2174/0929867322666150408111900.

Abstract

Epigenetic dysregulation has been recognized as an important contributor to cancer initiation and progression as most tumors harbor both genetic and epigenetic abnormalities. Inhibiting epigenetic proteins represents a novel approach in cancer drug discovery and more profound efficacy and less resistance are expected since multiple signaling pathways can be modulated as a result of inhibiting a single epigenetic target. Histone methyl transferases (HMTs) are an important component in epigenome and HMT inhibitors are being pursued intensely by both pharmaceutical industry and academic institutions. In this article we will provide an update on the drug discovery effort on several key HMTs.

摘要

表观遗传失调已被认为是癌症发生和进展的重要因素,因为大多数肿瘤都存在遗传和表观遗传异常。抑制表观遗传蛋白是癌症药物研发中的一种新方法,由于抑制单个表观遗传靶点可调节多种信号通路,因此有望获得更显著的疗效和更低的耐药性。组蛋白甲基转移酶(HMTs)是表观基因组的重要组成部分,制药行业和学术机构都在积极研发HMT抑制剂。在本文中,我们将提供关于几种关键HMTs药物研发工作的最新进展。

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