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MicroRNA Regulation of Cholesterol Metabolism

Disruption of cellular cholesterol balance results in pathologic processes including atherosclerosis, metabolic syndrome, type II diabetes and Alzheimer's disease. Maintenance of cholesterol homeostasis requires constant metabolic adjustment, achieved partly through the fine regulation of the c...

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Detalles Bibliográficos
Autores principales: Rotllan, Noemi, Fernández-Hernando, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420088/
https://www.ncbi.nlm.nih.gov/pubmed/22919472
http://dx.doi.org/10.1155/2012/847849
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author Rotllan, Noemi
Fernández-Hernando, Carlos
author_facet Rotllan, Noemi
Fernández-Hernando, Carlos
author_sort Rotllan, Noemi
collection PubMed
description Disruption of cellular cholesterol balance results in pathologic processes including atherosclerosis, metabolic syndrome, type II diabetes and Alzheimer's disease. Maintenance of cholesterol homeostasis requires constant metabolic adjustment, achieved partly through the fine regulation of the classical transcription factors (e.g., by SREBP and LXR), but also through members of a class of noncoding RNAs termed miRNAs. Some miRNAs have now been identified to be potent post-transcriptional regulators of lipid metabolism genes, including miR-122, miR-33, miR-758, and miR-106b. Different strategies have been developed to modulate miRNA effects for therapeutic purposes. The promise demonstrated by the use of anti-miRs in human preclinical studies, in the case of miR-122, raises the possibility that miR-33, miR-758, and miR-106b may become viable therapeutic targets in future. This review summarizes the evidence for a critical role of some miRNAs in regulating cholesterol metabolism and suggests novel ways to manage dyslipidemias and cardiovascular diseases.
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spelling pubmed-34200882012-08-23 MicroRNA Regulation of Cholesterol Metabolism Rotllan, Noemi Fernández-Hernando, Carlos Cholesterol Review Article Disruption of cellular cholesterol balance results in pathologic processes including atherosclerosis, metabolic syndrome, type II diabetes and Alzheimer's disease. Maintenance of cholesterol homeostasis requires constant metabolic adjustment, achieved partly through the fine regulation of the classical transcription factors (e.g., by SREBP and LXR), but also through members of a class of noncoding RNAs termed miRNAs. Some miRNAs have now been identified to be potent post-transcriptional regulators of lipid metabolism genes, including miR-122, miR-33, miR-758, and miR-106b. Different strategies have been developed to modulate miRNA effects for therapeutic purposes. The promise demonstrated by the use of anti-miRs in human preclinical studies, in the case of miR-122, raises the possibility that miR-33, miR-758, and miR-106b may become viable therapeutic targets in future. This review summarizes the evidence for a critical role of some miRNAs in regulating cholesterol metabolism and suggests novel ways to manage dyslipidemias and cardiovascular diseases. Hindawi Publishing Corporation 2012 2012-08-05 /pmc/articles/PMC3420088/ /pubmed/22919472 http://dx.doi.org/10.1155/2012/847849 Text en Copyright © 2012 N. Rotllan and C. Fernández-Hernando. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Rotllan, Noemi
Fernández-Hernando, Carlos
MicroRNA Regulation of Cholesterol Metabolism
title MicroRNA Regulation of Cholesterol Metabolism
title_full MicroRNA Regulation of Cholesterol Metabolism
title_fullStr MicroRNA Regulation of Cholesterol Metabolism
title_full_unstemmed MicroRNA Regulation of Cholesterol Metabolism
title_short MicroRNA Regulation of Cholesterol Metabolism
title_sort microrna regulation of cholesterol metabolism
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420088/
https://www.ncbi.nlm.nih.gov/pubmed/22919472
http://dx.doi.org/10.1155/2012/847849
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