EZH2型
表观遗传学
生物
组蛋白甲基转移酶
组蛋白
PRC2
癌症表观遗传学
甲基转移酶
表观遗传疗法
癌症
DNA甲基化
癌症研究
甲基化
计算生物学
遗传学
DNA
基因表达
基因
作者
Michael T. McCabe,Caretha L. Creasy
出处
期刊:Epigenomics
[Future Medicine]
日期:2014-06-01
卷期号:6 (3): 341-351
被引量:86
摘要
Over the last several years, dysregulation of epigenetic mechanisms including DNA and histone methylation has been recognized as a hallmark of cancer. Alterations of epigenetic regulators themselves, including the histone lysine methyltransferase EZH2, have been reported in numerous cancer types. With the discovery of small molecule inhibitors of EZH2, we can now begin to evaluate EZH2 as a therapeutic target in cancer. This article will provide an overview of the dysregulation of EZH2 in cancer, possible mechanisms for inhibition of EZH2 activity, and the preclinical activity of currently available EZH2 inhibitors.
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