The Mechanism Underlying the Regulation of Long Non-coding RNA MEG3 in Cerebral Ischemic Stroke

被引:8
作者
Zhao, Yanfang [1 ]
Liu, Yingying [2 ]
Zhang, Qili [1 ]
Liu, Hongliang [1 ]
Xu, Jianing [1 ]
机构
[1] Shandong Univ Technol, Zibo Key Lab New Drug Dev Neurodegenerat Dis, Shandong Prov Res Ctr Bioinformat Engn & Tech, Inst Biomed Res,Sch Life Sci & Med, Zibo, Peoples R China
[2] Hangzhou Normal Univ, Affiliated Hosp, Inst Translat Med, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
LncRNA; MEG3; Cerebral ischemic stroke; Neuronal cell death; Angiogenesis; LNCRNA MEG3; TRANSCRIPTOMIC PROFILES; NEURONAL APOPTOSIS; REPERFUSION INJURY; BRAIN; ANGIOGENESIS; CELLS; GENE; IMPAIRMENT; INFARCTION;
D O I
10.1007/s10571-021-01176-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cerebral ischemic stroke is one of the leading causes of morbidity and mortality worldwide, and rapidly increasing annually with no more effective therapeutic measures. Thus, the novel diagnostic and prognostic biomarkers are urgent to be identified for prevention and therapy of ischemic stroke. Recently, long noncoding RNAs (lncRNAs), a major family of noncoding RNAs with more than 200 nucleotides, have been considered as new targets for modulating pathological process of ischemic stroke. In this review, we summarized that the lncRNA-maternally expressed gene 3 (MEG3) played a critical role in promotion of neuronal cell death and inhibition of angiogenesis in response to hypoxia or ischemia condition, and further described the challenge of overcrossing blood-brain barrier (BBB) and determination of optimal carrier for delivering lncRNA' drugs into the specific brain regions. In brief, MEG3 will be a potential diagnostic biomarker and drug target in treatment and therapy of ischemic stroke in the future.
引用
收藏
页码:69 / 78
页数:10
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