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[微小RNA-21-5p通过靶向基因调控自噬的研究进展]

[Advance in research of microRNA-21-5p regulate autophagy by targeting gene].

作者信息

Liu Xinxin, Chen Miao, Chen Bowen, Feng Banghai

机构信息

Department of Critical Care Medicine, Affiliated Hospital of Zunyi Medical University, Zunyi 563000, Guizhou, China. Corresponding author: Chen Miao, Email:

出版信息

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2020 Jan;32(1):112-117. doi: 10.3760/cma.j.cn121430-20190925-00021.

Abstract

Autophagy is a dynamic process that degrades intracellular proteins and damaged organelles, and maintains environmental stability within the cell and provides good conditions for cell survival. Hyperoxic acute lung injury (HALI) is one of the serious complications of clinical oxygen therapy. The pathogenesis of HALI is still unclear. There are studies having shown that autophagy is involved in the pathogenesis of HALI. There are many pathway mechanisms that regulate autophagy, including phosphatidylinositol-3-kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR) signaling pathway, mitogen-activated protein kinase/extracellular signaling-regulated protein kinase (MAPK/ERK) signaling pathway, adenosine 5'-monophosphate-activated protein kinase/unc-51 like autophagy activating kinase 1 (AMPK/ULK1) signaling pathway, transforming growth factor β (TGF-β) and forkhead box O1 (FoxO1) and Ras guanosine triphosphatease superfamily member Rab11a, each of which is referred to as microRNA-21-5p (miR-21-5p) target gene having a role in regulating autophagy activity in many diseases. In this paper, the above-mentioned signaling pathways of miRNA-21-5p target genes regulating autophagy were reviewed in order to find clues about the mechanism of miRNA-21-5p regulating autophagy in HALI and provide a theoretical basis for subsequent basic research.

摘要

自噬是一个动态过程,可降解细胞内蛋白质和受损细胞器,维持细胞内环境稳定,为细胞存活提供良好条件。高氧急性肺损伤(HALI)是临床氧疗的严重并发症之一。HALI的发病机制尚不清楚。有研究表明自噬参与了HALI的发病机制。调节自噬的途径机制有很多,包括磷脂酰肌醇-3-激酶/蛋白激酶B/雷帕霉素靶蛋白(PI3K/Akt/mTOR)信号通路、丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)信号通路、5'-单磷酸腺苷激活蛋白激酶/类unc-51自噬激活激酶1(AMPK/ULK1)信号通路、转化生长因子β(TGF-β)和叉头框O1(FoxO1)以及Ras鸟苷三磷酸酶超家族成员Rab11a,它们各自被称为微小RNA-21-5p(miR-21-5p)的靶基因,在许多疾病中对调节自噬活性起作用。本文对上述miR-21-5p靶基因调节自噬的信号通路进行综述,以期找到miR-21-5p在HALI中调节自噬机制的线索,为后续基础研究提供理论依据。

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