靶向组蛋白赖氨酸去甲基酶家族的化学抑制剂与潜在的药物发现。

IF 2.5 Q3 GENETICS & HEREDITY Epigenomes Pub Date : 2023-03-11 DOI:10.3390/epigenomes7010007
Nando Dulal Das, Hideaki Niwa, Takashi Umehara
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引用次数: 1

摘要

组蛋白甲基化和去甲基化的动态调控在基因表达调控中起着重要作用。组蛋白赖氨酸去甲基化酶的异常表达与包括难治性癌症在内的多种疾病有关,因此赖氨酸去甲基化酶是有希望的治疗靶点。近年来,表观基因组学和化学生物学的研究导致了一系列小分子去甲基酶抑制剂的发展,这些抑制剂是有效的,特异性的,并且在体内有效。在这篇综述中,我们重点介绍了针对组蛋白赖氨酸去甲基化酶的新出现的小分子抑制剂及其在药物发现方面的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Chemical Inhibitors Targeting the Histone Lysine Demethylase Families with Potential for Drug Discovery.

The dynamic regulation of histone methylation and demethylation plays an important role in the regulation of gene expression. Aberrant expression of histone lysine demethylases has been implicated in various diseases including intractable cancers, and thus lysine demethylases serve as promising therapeutic targets. Recent studies in epigenomics and chemical biology have led to the development of a series of small-molecule demethylase inhibitors that are potent, specific, and have in vivo efficacy. In this review, we highlight emerging small-molecule inhibitors targeting the histone lysine demethylases and their progress toward drug discovery.

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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
期刊最新文献
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