Non-coding RNAs participate in the ischemia-reperfusion injury

被引:95
作者
Ghafouri-Fard, Soudeh [1 ]
Shoorei, Hamed [2 ]
Taheri, Mohammad [3 ]
机构
[1] Shahid Beheshti Univ Med Sci, Dept Med Genet, Tehran, Iran
[2] Birjand Univ Med Sci, Fac Med, Dept Anat Sci, Birjand, Iran
[3] Shahid Beheshti Univ Med Sci, Urogenital Stem Cell Res Ctr, Tehran, Iran
关键词
miRNA; lncRNA; Ischemia-reperfusion injury; MYOCARDIAL ISCHEMIA/REPERFUSION INJURY; NF-KAPPA-B; SIGNALING PATHWAY; DOWN-REGULATION; CELL APOPTOSIS; PROTECTS NEURONS; UP-REGULATION; RAT MODEL; CARDIOMYOCYTES; PI3K/AKT;
D O I
10.1016/j.biopha.2020.110419
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Ischemia, being defined as blood supply deficiency is involved in the pathogenesis of a number of life-threatening conditions such as myocardial infarction and cerebral stroke. Assessment of the molecular pathology of these conditions has led to identification of the role of reperfusion in induction and aggravation of tissue injury and necrosis. Thus, the term "ischemia/reperfusion (I/R) injury" has been introduced. This process involves aberrant regulation of the mitochondrial function, apoptotic and autophagic pathways and signal transducers. More recently, non-coding RNAs including long non-coding RNAs (lncRNAs) ad microRNAs (miRNAs) have been shown to influence I/R injury. Animal studies and clinical investigations have shown up-/down-regulation of tens of lncRNAs and miRNAs in this process. In the current study, we summarize the role of these transcripts in the pathophysiology of I/R injury and their potential as biomarkers for detection of extent of tissue injury.
引用
收藏
页数:15
相关论文
共 148 条
[1]
Bulkley G B, 1987, Br J Cancer Suppl, V8, P66
[2]
Knockdown of lncRNA Gm11974 protect against cerebral ischemic reperfusion through miR-766-3p/NR3C2 axis [J].
Cai, Jiangping ;
Shangguan, Shina ;
Li, Guoqian ;
Cai, Yazhen ;
Chen, Yuanjie ;
Ma, Gaoting ;
Miao, Zhongrong ;
Liu, Lian ;
Deng, Yiming .
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2019, 47 (01) :3847-3853
[3]
Chen Hong, 2019, Exp Mol Pathol, P104298, DOI 10.1016/j.yexmp.2019.104298
[4]
Upregulation of miR-1306-5p decreases cerebral ischemia/reperfusion injury in vitro by targeting BIK [J].
Chen, Xuelin ;
Li, Caixia ;
Li, Jianghao ;
Sheng, Luoping ;
Liu, Xianglu .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2019, 83 (12) :2230-2237
[5]
The role of microRNA-146a in regulating the expression of IRAK1 in cerebral ischemia-reperfusion injury [J].
Chu, Bo ;
Zhou, Yadong ;
Zhai, Heng ;
Li, Lei ;
Sun, Li ;
Li, Yun .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2018, 96 (06) :611-617
[6]
Suppression of Mouse AApoAII Amyloidosis Progression by Daily Supplementation with Oxidative Stress Inhibitors [J].
Dai, Jian ;
Ding, Xin ;
Miyahara, Hiroki ;
Xu, Zhe ;
Cui, Xiaoran ;
Igarashi, Yuichi ;
Sawashitaw, Jinko ;
Mori, Masayuki ;
Higuchi, Keiichi .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2019, 2019
[7]
miR-146a is essential for lipopolysaccharide (LPS)-induced cross-tolerance against kidney ischemia/reperfusion injury in mice [J].
Dai, Yan ;
Jia, Ping ;
Fang, Yi ;
Liu, Hong ;
Jiao, Xiaoyan ;
He, John C. ;
Ding, Xiaoqiang .
SCIENTIFIC REPORTS, 2016, 6
[8]
Di YF, 2017, AM J TRANSL RES, V9, P656
[9]
Inhibiting MicroRNA-29a Protects Myocardial Ischemia-Reperfusion Injury by Targeting SIRT1 and Suppressing Oxidative Stress and NLRP3-Mediated Pyroptosis Pathway [J].
Ding, Shoukun ;
Liu, Donghai ;
Wang, Lixia ;
Wang, Guanggong ;
Zhu, Yaobin .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2020, 372 (01) :128-135
[10]
Inhibition of Smurf2 translation by miR-322/503 protects from ischemia-reperfusion injury by modulating EZH2/Akt/GSK3β signaling [J].
Dong, Wei ;
Xie, Fei ;
Chen, Xuan-Ying ;
Huang, Wei-Lin ;
Zhang, Yu-Zhen ;
Luo, Wen-Bo ;
Chen, Jin ;
Xie, Ming-Tuan ;
Peng, Xiao-Ping .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2019, 317 (02) :C253-C261