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表观遗传机制与动脉粥样硬化中转录因子的相互作用。

Interplay between epigenetic mechanisms and transcription factors in atherosclerosis.

机构信息

Department of Diabetes, Central Clinical School, Monash University, Melbourne, Australia.

Department of Diabetes, Central Clinical School, Monash University, Melbourne, Australia; German Diabetes Centre, Leibniz Centre for Diabetes Research at the Heinrich Heine University, Dusseldorf, Germany.

出版信息

Atherosclerosis. 2024 Aug;395:117615. doi: 10.1016/j.atherosclerosis.2024.117615. Epub 2024 Jun 6.

Abstract

Cardiovascular diseases (CVD), including coronary heart disease and stroke, comprise the number one cause of mortality worldwide. A major contributor to CVD is atherosclerosis, which is a low-grade inflammatory disease of vasculature that involves a pathological build-up of plaque within the arterial walls. Studies have shown that regulation of gene expression via transcription factors and epigenetic mechanisms play a fundamental role in transcriptomic changes linked to the development of atherosclerosis. Chromatin remodeling is a reversible phenomenon and studies have supported the clinical application of chromatin-modifying agents for the prevention and treatment of CVD. In addition, pre-clinical studies have identified multiple transcription factors as potential therapeutic targets in combating atherosclerotic CVD. Although interaction between transcription factors and epigenetic mechanisms facilitate gene regulation, a limited number of studies appreciate this crosstalk in the context of CVD. Here, we reviewed this gene regulatory mechanism underappreciated in atherosclerosis, which will highlight the mechanisms underlying novel therapeutics targeting epigenetic modifiers and transcription factors in atherosclerosis.

摘要

心血管疾病(CVD),包括冠心病和中风,是全球头号死因。CVD 的一个主要诱因是动脉粥样硬化,这是一种血管的低度炎症性疾病,涉及动脉壁内斑块的病理性堆积。研究表明,转录因子和表观遗传机制对基因表达的调控在与动脉粥样硬化发展相关的转录组变化中起着至关重要的作用。染色质重塑是一种可逆的现象,研究支持使用染色质修饰剂来预防和治疗 CVD。此外,临床前研究已经确定了多种转录因子作为对抗动脉粥样硬化性 CVD 的潜在治疗靶点。尽管转录因子和表观遗传机制之间的相互作用有助于基因调控,但很少有研究在 CVD 背景下关注这种串扰。在这里,我们回顾了在动脉粥样硬化中被低估的这种基因调控机制,这将突出针对动脉粥样硬化中表观遗传修饰剂和转录因子的新型治疗方法的潜在机制。

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