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EZH2 作为癌症治疗的潜在靶点。

EZH2 as a potential target in cancer therapy.

机构信息

Cancer Epigenetics Discovery Performance Unit, Oncology R&D, GlaxoSmithKline, 1250 S. Collegeville Road, Collegeville, PA 19426, USA.

出版信息

Epigenomics. 2014 Jun;6(3):341-51. doi: 10.2217/epi.14.23.

Abstract

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.

摘要

在过去的几年中,人们已经认识到包括 DNA 和组蛋白甲基化在内的表观遗传机制的失调是癌症的一个标志。在许多癌症类型中,已经报道了表观遗传调节剂本身的改变,包括组蛋白赖氨酸甲基转移酶 EZH2。随着 EZH2 的小分子抑制剂的发现,我们现在可以开始评估 EZH2 在癌症中的治疗靶点。本文将概述 EZH2 在癌症中的失调、抑制 EZH2 活性的可能机制以及目前可用的 EZH2 抑制剂的临床前活性。

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