miR-210: The Master Hypoxamir

被引:350
作者
Chan, Yuk C. [1 ]
Banerjee, Jaideep [1 ]
Choi, Sang Yong [1 ]
Sen, Chandan K. [1 ]
机构
[1] Ohio State Univ, Dept Surg, Davis Heart & Lung Res Inst, Med Ctr, Columbus, OH 43210 USA
关键词
miR-210; hypoxamiRs; microRNAs; tissue repair; GROWTH-FACTOR RECEPTOR; CYTOCHROME-C-OXIDASE; ARTERY BYPASS; CELL-CYCLE; INFRAINGUINAL BYPASS; CIRCULATING MIR-210; PROGNOSTIC-FACTOR; PERONEAL BYPASS; GENE-EXPRESSION; LIMB SALVAGE;
D O I
10.1111/j.1549-8719.2011.00154.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
MicroRNAs are small non-coding RNAs implicated mainly in post-transcriptional gene silencing by interacting with the untranslated region of the transcript. miR-210 represents major hypoxia-inducible miRs, also known as hypoxamirs, which is ubiquitously expressed in a wide range of cells, serving versatile functions. This review article summarizes the current progress on biogenesis of miR-210 and its physiological roles including arrest of cell proliferation, repression of mitochondrial respiration, arrest of DNA repair, vascular biology, and angiogenesis. Given the fact that miR-210 is aberrantly expressed in a number of diseases such as tumor progression, myocardial infarction and cutaneous ischemic wounds, miR-210 could serve as an excellent candidate for prognostic purposes and therapeutic intervention. With the advancement of computational prediction, high-throughput target validation methodology, sequencing, proteomic analysis, and microarray, it is anticipated that more down-stream targets of miR-210 and its associated biological consequences under hypoxia will be unveiled establishing miR-210 as a major hub in the biology of hypoxia-response.
引用
收藏
页码:215 / 223
页数:9
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