小RNA
阿佩林
串扰
信号转导
血管紧张素II
MAPK/ERK通路
血压
生物
生物信息学
受体
医学
细胞生物学
内分泌学
遗传学
基因
光学
物理
作者
Farman Ali,Aling Shen,Waqar Islam,Muhammad Zubair Saleem,Ragunath Muthu,Qiurong Xie,Meizhu Wu,Ying Cheng,Jiangfeng Chu,Wei Lin,Jun Peng
标识
DOI:10.1016/j.micpath.2021.105361
摘要
Hypertension is controlled via the alteration of microRNAs (miRNAs), their therapeutic targets angiotensin II type I receptor (AT1R) and cross talk of signaling pathways. The stimulation of the Ang II/AT1R pathway by deregulation of miRNAs, has also been linked to cardiac remodeling as well as the pathophysiology of high blood pressure. As miRNAs have been associated to ACE2/Apelin and Mitogen-activated protein kinases (MAPK) signaling, it has revealed an utmost protective impact over hypertension and cardiovascular system. The ACE2-coupled intermodulation between RAAS, Apelin system, MAPK signaling pathways, and miRNAs reveal the practicalities of high blood pressure. The research of miRNAs may ultimately lead to the expansion of an innovative treatment strategy for hypertension, which indicates the need to explore them further at the molecular level. Therefore, here we have focused on the mechanistic importance of miRNAs in hypertension, ACE2/Apelin signaling as well as their biological functions, with a focus on interplay and crosstalk between ACE2/Apelin signaling, miRNAs, and hypertension, and the progress in miRNA-based diagnostic techniques with the goal of facilitating the development of new hypertension-controlling therapeutics.
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