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miR-21 in ischemia/reperfusion injury: a double-edged sword?
Author(s) -
Xialian Xu,
Alison J. Kriegel,
Xiaoyan Jiao,
Hong Liu,
Xiaowen Bai,
Jessica Olson,
Mingyu Liang,
Xiaoqiang Ding
Publication year - 2014
Publication title -
physiological genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.078
H-Index - 112
eISSN - 1531-2267
pISSN - 1094-8341
DOI - 10.1152/physiolgenomics.00020.2014
Subject(s) - biology , microrna , angiogenesis , reperfusion injury , inflammation , ischemia , downregulation and upregulation , acute kidney injury , fibrosis , cancer research , immunology , bioinformatics , pathology , gene , medicine , genetics
MicroRNAs (miRNAs or miRs) are endogenous, small RNA molecules that suppress expression of targeted mRNA. miR-21, one of the most extensively studied miRNAs, is importantly involved in divergent pathophysiological processes relating to ischemia/reperfusion (I/R) injury, such as inflammation and angiogenesis. The role of miR-21 in renal I/R is complex, with both protective and pathological pathways being regulated by miR-21. Preconditioning-induced upregulation of miR-21 contributes to the protection against subsequent renal I/R injury through the targeting of genes such as the proapoptotic gene programmed cell death 4 and interactions between miR-21 and hypoxia-inducible factor. Conversely, long-term elevation of miR-21 may be detrimental to the organ by promoting the development of renal interstitial fibrosis following I/R injury. miR-21 is importantly involved in several pathophysiological processes related to I/R injury including inflammation and angiogenesis as well as the biology of stem cells that could be used to treat I/R injury; however, the effect of miR-21 on these processes in renal I/R injury remains to be studied.

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