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DNA 甲基转移酶抑制剂在癌症治疗中的应用:化学和治疗专利概述及部分临床研究

DNA methyltransferase inhibitors in cancer: a chemical and therapeutic patent overview and selected clinical studies.

机构信息

USR 3388 Epigenetic Targeting of Cancer, CNRS-Pierre Fabre, CRDPF, BP 13562, 3 avenue Hubert Curien, 31 035 Toulouse CEDEX 01, France.

出版信息

Expert Opin Ther Pat. 2012 Dec;22(12):1427-42. doi: 10.1517/13543776.2012.729579. Epub 2012 Oct 3.

Abstract

INTRODUCTION

DNA methylation is an epigenetic modification that modulates gene expression without altering the DNA base sequence. It plays a crucial role in cancer by silencing tumor suppressor genes (TSG). The DNA methyltransferases (DNMT) are the enzymes that catalyze DNA methylation and they are interesting therapeutical targets since DNA methylation is reversible such that an aberrant hypermethylation of DNA can be reverted by inhibition of DNMTs. Today, two drugs are on the market for the treatment of myelodysplastic syndrome, azacitidine and decitabine.

AREAS COVERED

Here, we present a review of the patents describing the chemistry and biological activities of novel DNMT inhibitors and discuss select clinical studies.

EXPERT OPINION

DNMT inhibitors have shown efficacy in clinics. However, highly efficient and specific DNMT inhibitors have not yet been identified. Improving methods will certainly lead to the prediction of novel directly binding inhibitors in the future.

摘要

简介

DNA 甲基化是一种表观遗传修饰,它在不改变 DNA 碱基序列的情况下调节基因表达。它通过沉默肿瘤抑制基因(TSG)在癌症中起着至关重要的作用。DNA 甲基转移酶(DNMT)是催化 DNA 甲基化的酶,由于 DNA 甲基化是可逆的,因此异常的 DNA 高甲基化可以通过抑制 DNMT 来逆转,因此它们是有趣的治疗靶点。如今,有两种药物上市用于治疗骨髓增生异常综合征,阿扎胞苷和地西他滨。

涵盖领域

在这里,我们回顾了描述新型 DNMT 抑制剂的化学和生物学活性的专利,并讨论了一些临床研究。

专家意见

DNMT 抑制剂在临床上已显示出疗效。然而,尚未发现高效和特异性的 DNMT 抑制剂。改进方法肯定会导致未来新型直接结合抑制剂的预测。

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