长链非编码RNA H19在肺动脉高压相关右心衰中的作用

J. Omura, K. Habbout, S. Martineau, S. Breuils-bonnet, V. Nadeau, F. Potus, Stephen L. Archer, R. Paulin, S. Provencher, O. Boucherat, S. Bonnet
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引用次数: 3

摘要

背景:右心室衰竭(RVF)是肺动脉高压(PAH)的主要预后因素。最近的组学分析表明,在左心衰过程中,一些长链非编码rna (LncRNAs)被解除管制,但它们在裂谷热中的作用尚不清楚。LncRNA H19及其编码的miR-675与心脏肥大和纤维化(裂谷热的两个特征)有关,但从未在裂谷热中进行过研究。方法和结果:通过qRT-PCR,我们发现从对照供体、代偿性右心室肥大患者(CRVH, Cardiac index > 2.2)和失代偿性右心室肥大患者(DRVH,死于RVF的PAH患者)获得的人类右心室活检中,H19和miR-675特异性上调(p结论:我们首次证明H19参与了人类RVF从CRVH向DRVH的转变。循环H19是PAH患者RV功能的推定生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long Non-coding RNA H19 in Right Ventricular Failure associated with Pulmonary Arterial Hypertension
Background: Right ventricular failure (RVF) is the major prognostic factor in pulmonary arterial hypertension (PAH). Recent Omics analyses have demonstrated the deregulation of several long non-coding RNAs (LncRNAs) in left heart failure, but their role in RVF remains unknown. The LncRNA H19 and its encoded miR-675 have been implicated in both cardiac hypertrophy and fibrosis (2 features of RVF) but never been studied in RVF. Methods and Results: By qRT-PCR, we showed in human RV biopsies obtained from control donors, compensated RV hypertrophy patients (CRVH, Cardiac index > 2.2) and decompensated RV hypertrophy patients (DRVH, PAH patients that died from RVF), that H19 and miR-675 were specifically up-regulated (p Conclusions: We demonstrated for the first time that H19 is implicated in the transition from CRVH to DRVH in human RVF. Circulating H19 represents a putative biomarker of RV function in PAH patients.
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