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用小分子靶向DNA甲基化:接下来会怎样?

Targeting DNA methylation with small molecules: what's next?

作者信息

Erdmann Alexandre, Halby Ludovic, Fahy Jacques, Arimondo Paola B

机构信息

Epigenetic Targeting of Cancer, USR3388 ETaC, CNRS-Pierre Fabre, 3 Avenue H. Curien, 31035 Toulouse Cedex 01, France.

出版信息

J Med Chem. 2015 Mar 26;58(6):2569-83. doi: 10.1021/jm500843d. Epub 2014 Dec 4.

Abstract

DNA methylation is a mammalian epigenetic mark that is involved in defining where and when genes are expressed, both in normal cells and in the context of diseases. Like other epigenetic marks, it is reversible and can be modulated by chemical agents. Because it plays an important role in cancer by silencing certain genes, such as tumor suppressor genes, and by reactivating other regions, such as repeated elements, it is a promising therapeutic target. Two compounds are already approved to treat hematological cancers. Many efforts have been carried out to discover new molecules that are able to efficiently inhibit DNA methylation in cancer cells. We will briefly overview the foremost of these efforts by focusing on what we have learned to this point on non-nucleoside inhibitors and on what we consider to be the features of an ideal inhibitor.

摘要

DNA甲基化是一种哺乳动物表观遗传标记,在正常细胞和疾病背景下,它都参与决定基因表达的位置和时间。与其他表观遗传标记一样,它是可逆的,并且可以被化学试剂调节。由于它通过使某些基因(如肿瘤抑制基因)沉默以及使其他区域(如重复元件)重新激活,在癌症中发挥重要作用,因此它是一个有前景的治疗靶点。已有两种化合物被批准用于治疗血液系统癌症。人们已经开展了许多工作来发现能够有效抑制癌细胞中DNA甲基化的新分子。我们将通过重点介绍我们目前对非核苷抑制剂的了解以及我们认为理想抑制剂的特征,简要概述这些最重要的工作。

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