肺动脉高压微rna通路损伤初期的DNA损伤

F. Potus, M. Leguen, S. Provencher, J. Meloche, S. Bonnet
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引用次数: 1

摘要

在过去的几年里,小的非编码microrna (mirna)已经成为PAH病因学的核心参与者。PAH患者的肺和右心室(RV)均出现较强的miRNA表达紊乱,分别导致肺动脉远端血管重构和右心室衰竭。另一方面,随着DNA损伤和DNA损伤反应(DDR)在该疾病中的作用,我们对多环芳烃生理病理的理解最近有所增加。有趣的是,DDR被描述为健康和病理条件下miRNA加工的调节因子。在这篇综述中,我们将首先总结PAH患者肺和右心室的miRNA表达受损,然后我们将提供证据,证明DDR可能是肺动脉高压中观察到的miRNA通路缺陷的起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DNA damage at the dawn of micro-RNA pathway impairment in pulmonary arterial hypertension
Over the last years, small non-coding microRNAs (miRNAs) have emerged as central actors of PAH etiology. Strong miRNA expression disorders occur in lungs as well as in right ventricle (RV) of PAH patients, which respectively lead to vascular remodeling of the distal pulmonary arteries and to RV failure. On the other hand, our understanding of PAH physiopathology has recently increased with the implication of DNA damage and DNA damage response (DDR) in this disease. Interestingly, DDR was described as a regulator of miRNA processing in both healthy and pathological conditions. In this review, we will first summarize miRNA expression impaired in lung and RV of PAH patients, then we will provide evidence that DDR could be at origin of miRNA pathway defects observed in pulmonary hypertension.
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