子宫内膜异位症
组蛋白
锡尔图因
背景(考古学)
组蛋白脱乙酰基酶2
医学
表观遗传学
生物信息学
染色质
癌症研究
组蛋白脱乙酰基酶
生物
内科学
遗传学
乙酰化
基因
古生物学
作者
Iason Psilopatis,Kleio Vrettou,Florian Nima Fleckenstein,Stamatios Theocharis
出处
期刊:Cells
[MDPI AG]
日期:2023-04-23
卷期号:12 (9): 1227-1227
被引量:8
标识
DOI:10.3390/cells12091227
摘要
Endometriosis is a chronic disorder of the female reproductive system which afflicts a great number of women worldwide. Histone deacetylases (HDACs) prevent the relaxation of chromatin, thereby positively or negatively modulating gene transcription. The current review aims at studying the impact of histone modifications and their therapeutic targeting in endometriosis. In order to identify relevant studies, a literature review was conducted using the MEDLINE and LIVIVO databases. The current manuscript represents the most comprehensive, up-to-date review of the literature focusing on the particular role of HDACs and their inhibitors in the context of endometriosis. HDAC1, HDAC2, HDAC3, Sirtuin 1, and Sirtuin 3, are the five most studied HDAC enzymes which seem to, at least partly, influence the pathophysiology of endometriosis. Both well-established and novel HDACIs could possibly represent modern, efficacious anti-endometriotic drug agents. Altogether, histone modifications and their therapeutic targeting have been proven to have a strong impact on endometriosis.
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