MicroRNA-210 A unique and pleiotropic hypoxamir

被引:377
作者
Chan, Stephen Y. [2 ]
Loscalzo, Joseph [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc Med,Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Cardiol,Dept Med, Boston, MA USA
关键词
microRNA; hypoxia; miR-210; hypoxia inducible factor; metabolism; proliferation; angiogenesis; apoptosis; cell cycle; Pasteur effect; SULFUR CLUSTER BIOGENESIS; RECEPTOR TYROSINE KINASE; REPAIR GENE-EXPRESSION; ESCHERICHIA-COLI; MESSENGER-RNAS; NITRIC-OXIDE; DNA-REPAIR; HYPOXIA; PROTEIN; MIR-210;
D O I
10.4161/cc.9.6.11006
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Inadequate oxygen availability or hypoxia induces a complex and still incompletely understood set of adaptations that influence cellular survival and function. Many of these adaptations are directly controlled by a master transcription factor, hypoxia inducible factor-alpha (HIF-alpha). In response to hypoxia, HIF-alpha levels increase and directly induce the transcription of > 100 genes, influencing functions ranging from metabolism, survival, proliferation, migration, to angiogenesis, among others. Recently, it has been demonstrated that a specific set of microRNA molecules are upregulated by hypoxia, which we denote here as "hypoxamirs." In particular, the HIF-responsive hypoxamir microRNA-210 (miR-210) is a unique microRNA that is evolutionarily conserved and ubiquitously expressed in hypoxic cell and tissue types. A number of direct targets of miR-210 have been identified by in silico, transcriptional and biochemical methods, a subset of which have been extensively validated. As a result, miR-210 has been mechanistically linked to the control of a wide range of cellular responses known to influence normal developmental physiology as well as a number of hypoxia-dependent disease states, including tissue ischemia, inflammation and tumorigenesis. Thus, reflecting the pleiotropic actions of HIF-alpha, miR-210 appears to function as a "master microRNA" relevant for the control of diverse functions in the hypoxic state.
引用
收藏
页码:1072 / 1083
页数:12
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