心肌保护
小RNA
缺血
转录因子
氧化应激
再灌注损伤
生物信息学
医学
药理学
心脏病学
生物
内科学
细胞生物学
基因
遗传学
作者
András Makkos,Bence Ágg,Balázs Petrovich,Zoltán V. Varga,Anikó Görbe,Péter Ferdinandy
标识
DOI:10.1016/j.freeradbiomed.2021.04.034
摘要
Although myocardial ischemia-reperfusion injury (I/R) and its pathological consequences are the leading cause of morbidity and mortality worldwide, cardioprotective therapeutics are still not on the market. Oxidative stress, a major contributing factor to myocardial I/R, changes transcription of coding and non-coding RNAs, alters post-transcriptional modulations, and regulate protein function. MicroRNA (miRNA) expression can be altered by oxidative stress and microRNAs may also regulate cytoprotective mechanisms and exert cardioprotection againts I/R. Transcriptomic analysis of I/R and oxidative stress-induced alterations followed by microRNA-mRNA target interaction network analysis may reveal microRNAs and their mRNA targets that may play a role in cardioprotection and serve as microRNA therapeutics or novel molecular targets for further drug development. Here we provide a summary of a systematic literature review and in silico molecular network analysis to reveal important cardioprotective microRNAs and their molecular targets that may provide cardioprotection via regulation of redox signalling.
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