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MEK-ERK-Egr-1轴及其在心血管疾病中的调控

The MEK-ERK-Egr-1 axis and its regulation in cardiovascular disease.

作者信息

Khachigian Levon M

机构信息

Vascular Biology and Translational Research, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Vascul Pharmacol. 2023 Dec;153:107232. doi: 10.1016/j.vph.2023.107232. Epub 2023 Sep 20.

Abstract

Cardiovascular disease (CVD) is the primary cause of morbidity and mortality in the Western world. Multiple molecular and cellular processes underpinning the pathogenesis of CVD are regulated by the zinc finger transcription factor and product of an immediate-early gene, early growth response-1 (Egr-1). Egr-1 regulates multiple pro-inflammatory processes that underpin the manifestation of CVD. The activity of Egr-1 itself is influenced by a range of post-translational modifications including sumoylation, ubiquitination and acetylation. Egr-1 also undergoes phosphorylation by protein kinases, such as extracellular-signal regulated kinase (ERK) which is itself phosphorylated by MEK. This article reviews recent progress on the MEK-ERK-Egr-1 cascade, notably regulation in conjunction with factors and agents such as TET2, TRIB2, MIAT, SphK1, cAMP, teneligliptin, cholinergic drugs, red wine and flavonoids, wogonin, febuxostat, docosahexaenoic acid and AT1R blockade. Such insights should provide new opportunity for therapeutic intervention in CVD.

摘要

心血管疾病(CVD)是西方世界发病和死亡的主要原因。锌指转录因子和即早基因早期生长反应-1(Egr-1)的产物调节着CVD发病机制背后的多个分子和细胞过程。Egr-1调节多种促炎过程,这些过程是CVD表现的基础。Egr-1自身的活性受一系列翻译后修饰的影响,包括SUMO化、泛素化和乙酰化。Egr-1还会被蛋白激酶磷酸化,如细胞外信号调节激酶(ERK),而ERK本身又会被MEK磷酸化。本文综述了MEK-ERK-Egr-1级联反应的最新进展,特别是与TET2、TRIB2、MIAT、SphK1、cAMP、替格列汀、胆碱能药物、红酒和类黄酮、汉黄芩素、非布司他、二十二碳六烯酸和血管紧张素II 1型受体(AT1R)阻断等因子和药物相关的调节。这些见解应为CVD的治疗干预提供新的机会。

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