Literature DB >> 24053126

HypoxamiR regulation and function in ischemic cardiovascular diseases.

Simona Greco1, Carlo Gaetano, Fabio Martelli.   

Abstract

SIGNIFICANCE: MicroRNAs (miRNAs) are deregulated and play a causal role in numerous cardiovascular diseases, including myocardial infarction, coronary artery disease, hypertension, heart failure, stroke, peripheral artery disease, kidney ischemia-reperfusion. RECENT ADVANCES: One crucial component of ischemic cardiovascular diseases is represented by hypoxia. Indeed, hypoxia is a powerful stimulus regulating the expression of a specific subset of miRNAs, named hypoxia-induced miRNAs (hypoxamiR). These miRNAs are fundamental regulators of the cell responses to decreased oxygen tension. Certain hypoxamiRs seem to have a particularly pervasive role, such as miR-210 that is virtually induced in all ischemic diseases tested so far. However, its specific function may change according to the physiopathological context. CRITICAL ISSUES: The discovery of HypoxamiR dates back 6 years. Thus, despite a rapid growth in knowledge and attention, a deeper insight of the molecular mechanisms underpinning hypoxamiR regulation and function is needed. FUTURE DIRECTIONS: An extended understanding of the function of hypoxamiR in gene regulatory networks associated with cardiovascular diseases will allow the identification of novel molecular mechanisms of disease and indicate the development of innovative therapeutic approaches.

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Year:  2013        PMID: 24053126      PMCID: PMC4142792          DOI: 10.1089/ars.2013.5403

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  161 in total

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Review 2.  Oxygen sensing, homeostasis, and disease.

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4.  Increased microRNA-1 and microRNA-133a levels in serum of patients with cardiovascular disease indicate myocardial damage.

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Journal:  Circ Cardiovasc Genet       Date:  2011-06-02

5.  Hypoxia potentiates microRNA-mediated gene silencing through posttranslational modification of Argonaute2.

Authors:  Connie Wu; Jessica So; Brandi N Davis-Dusenbery; Hank H Qi; Donald B Bloch; Yang Shi; Giorgio Lagna; Akiko Hata
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6.  MicroRNA-155 promotes resolution of hypoxia-inducible factor 1alpha activity during prolonged hypoxia.

Authors:  Ulrike Bruning; Luca Cerone; Zoltan Neufeld; Susan F Fitzpatrick; Alex Cheong; Carsten C Scholz; David A Simpson; Martin O Leonard; Murtaza M Tambuwala; Eoin P Cummins; Cormac T Taylor
Journal:  Mol Cell Biol       Date:  2011-08-01       Impact factor: 4.272

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8.  microRNA-210 is upregulated in hypoxic cardiomyocytes through Akt- and p53-dependent pathways and exerts cytoprotective effects.

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Authors:  A Magenta; C Cencioni; P Fasanaro; G Zaccagnini; S Greco; G Sarra-Ferraris; A Antonini; F Martelli; M C Capogrossi
Journal:  Cell Death Differ       Date:  2011-04-29       Impact factor: 15.828

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  42 in total

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2.  Involvement of the miR-462/731 cluster in hypoxia response in Megalobrama amblycephala.

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Review 3.  The epigenetic landscape related to reactive oxygen species formation in the cardiovascular system.

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Journal:  Br J Pharmacol       Date:  2017-05-10       Impact factor: 8.739

4.  miR-200b downregulates Kruppel Like Factor 2 (KLF2) during acute hypoxia in human endothelial cells.

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5.  The hypoxia-inducible miR-429 regulates hypoxia-inducible factor-1α expression in human endothelial cells through a negative feedback loop.

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7.  Circulating MicroRNAs as Potential Biomarkers for Ischemic Stroke in Patients with Asymptomatic Intracranial Artery Stenosis.

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Review 8.  MicroRNAs in endothelial cell homeostasis and vascular disease.

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9.  MiR-221-3p targets Hif-1α to inhibit angiogenesis in heart failure.

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10.  miR-210 Enhances the Therapeutic Potential of Bone-Marrow-Derived Circulating Proangiogenic Cells in the Setting of Limb Ischemia.

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Journal:  Mol Ther       Date:  2018-06-15       Impact factor: 11.454

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