Literature DB >> 27544699

MicroRNAs in heart failure: Non-coding regulators of metabolic function.

Xiaokan Zhang1, P Christian Schulze2.   

Abstract

Heart failure (HF) is the inability of the heart to provide sufficient cardiac output for the energy demands of the body. Over the last decades, our understanding of the role of microRNAs (miRNAs), a class of small non-coding RNA regulators of gene expression at the post-transcriptional level, in cardiovascular diseases has expanded at a rapid rate. Importantly, multiple miRNAs have been specifically implicated in the progression of HF. Growing evidence suggests that miRNAs regulate central metabolic pathways and thus are highly implicated in the maintenance of energy homeostasis. In this review, we highlight recent discoveries of the mechanistic role of miRNAs in regulating metabolic functions in HF, with specific focus on the implication of miRNAs in metabolic rearrangements, discuss the potential value of miRNA profiles as novel HF biomarkers, and summarize the recent investigations on therapeutic approaches using miRNAs in heart disease. This article is part of a Special Issue entitled: The role of post-translational protein modifications on heart and vascular metabolism edited by Jason R.B. Dyck & Jan F.C. Glatz.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Heart failure; Metabolism; MicroRNA

Mesh:

Substances:

Year:  2016        PMID: 27544699      PMCID: PMC5376502          DOI: 10.1016/j.bbadis.2016.08.009

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  171 in total

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2.  Hepatic SREBP-2 and cholesterol biosynthesis are regulated by FoxO3 and Sirt6.

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3.  SIRT3 deacetylates ATP synthase F1 complex proteins in response to nutrient- and exercise-induced stress.

Authors:  Athanassios Vassilopoulos; J Daniel Pennington; Thorkell Andresson; David M Rees; Allen D Bosley; Ian M Fearnley; Amy Ham; Charles Robb Flynn; Salisha Hill; Kristie Lindsey Rose; Hyun-Seok Kim; Chu-Xia Deng; John E Walker; David Gius
Journal:  Antioxid Redox Signal       Date:  2014-03-06       Impact factor: 8.401

4.  MicroRNAs in metabolism and metabolic diseases.

Authors:  V Rottiers; S H Najafi-Shoushtari; F Kristo; S Gurumurthy; L Zhong; Y Li; D E Cohen; R E Gerszten; N Bardeesy; R Mostoslavsky; A M Näär
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2011-12-12

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7.  Control of mitochondrial metabolism and systemic energy homeostasis by microRNAs 378 and 378*.

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10.  The hypoxia-inducible microRNA cluster miR-199a∼214 targets myocardial PPARδ and impairs mitochondrial fatty acid oxidation.

Authors:  Hamid el Azzouzi; Stefanos Leptidis; Ellen Dirkx; Joris Hoeks; Bianca van Bree; Karl Brand; Elizabeth A McClellan; Ella Poels; Judith C Sluimer; Maarten M G van den Hoogenhof; Anne-Sophie Armand; Xiaoke Yin; Sarah Langley; Meriem Bourajjaj; Serve Olieslagers; Jaya Krishnan; Marc Vooijs; Hiroki Kurihara; Andrew Stubbs; Yigal M Pinto; Wilhelm Krek; Manuel Mayr; Paula A da Costa Martins; Patrick Schrauwen; Leon J De Windt
Journal:  Cell Metab       Date:  2013-09-03       Impact factor: 27.287

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4.  Circulating MicroRNAs and myocardial involvement severity in chronic Chagas cardiomyopathy.

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Review 6.  Regulating microRNA expression: at the heart of diabetes mellitus and the mitochondrion.

Authors:  Quincy A Hathaway; Mark V Pinti; Andrya J Durr; Shanawar Waris; Danielle L Shepherd; John M Hollander
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7.  Differential Expression Profiles of Mitogenome Associated MicroRNAs Among Colorectal Adenomatous Polyps.

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8.  The Profiling and Role of miRNAs in Diabetes Mellitus.

Authors:  Michael Kim; Xiaokan Zhang
Journal:  J Diabetes Clin Res       Date:  2019

9.  Circulating miR-499a and miR-125b as Potential Predictors of Left Ventricular Ejection Fraction Improvement after Cardiac Resynchronization Therapy.

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  9 in total

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