Literature DB >> 26869447

miRNAs and High-Density Lipoprotein metabolism.

Ángel Baldán1, Thomas Q de Aguiar Vallim2.   

Abstract

Altered lipoprotein metabolism plays a key role during atherogenesis. For over 50years, epidemiological data have fueled the proposal that HDL-cholesterol (HDL-c) in circulation is inversely correlated to cardiovascular risk. However, the atheroprotective role of HDL is currently the focus of much debate and remains an active field of research. The emerging picture from research in the past decade suggests that HDL function, rather than HDL-c content, is important in disease. Recent developments demonstrate that miRNAs play an important role in fine-tuning the expression of key genes involved in HDL biogenesis, lipidation, and clearance, as well as in determining the amounts of HDL-c in circulation. Thus, it has been proposed that miRNAs that affect HDL metabolism might be exploited therapeutically in patients. Whether HDL-based therapies, alone or in combination with LDL-based treatments (e.g. statins), provide superior outcomes in patients has been recently questioned by human genetics studies and clinical trials. The switch in focus from "HDL-cholesterol" to "HDL function" opens a new paradigm to understand the physiology and therapeutic potential of HDL, and to find novel modulators of cardiovascular risk. In this review we summarize the current knowledge on the regulation of HDL metabolism and function by miRNAs. This article is part of a Special Issue entitled: MicroRNAs and lipid/energy metabolism and related diseases edited by Carlos Fernández-Hernando and Yajaira Suárez.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Atherosclerosis; Cardiovascular disease; Cholesterol; HDL; Lipoproteins; miRNA

Mesh:

Substances:

Year:  2016        PMID: 26869447      PMCID: PMC4980286          DOI: 10.1016/j.bbalip.2016.01.021

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


  112 in total

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Review 6.  Transcriptional integration of metabolism by the nuclear sterol-activated receptors LXR and FXR.

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7.  Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia.

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Authors:  Thomas Q de Aguiar Vallim; Elizabeth J Tarling; Peter A Edwards
Journal:  Cell Metab       Date:  2013-04-18       Impact factor: 27.287

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Authors:  Noam Zelcer; Cynthia Hong; Rima Boyadjian; Peter Tontonoz
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4.  Profiling of circulating chromosome 21-encoded microRNAs, miR-155, and let-7c, in down syndrome.

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