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Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction

The rapid rise of type II diabetes mellitus and its accompanying vascular complications call for novel approaches in unravelling its pathophysiological mechanisms and designing new treatment modalities. Noncoding RNAs represent a class of previously unknown molecular modulators of this disease. The...

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Detalles Bibliográficos
Autores principales: Eken, Suzanne M., Jin, Hong, Chernogubova, Ekaterina, Maegdefessel, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863503/
https://www.ncbi.nlm.nih.gov/pubmed/24369540
http://dx.doi.org/10.1155/2013/834727
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author Eken, Suzanne M.
Jin, Hong
Chernogubova, Ekaterina
Maegdefessel, Lars
author_facet Eken, Suzanne M.
Jin, Hong
Chernogubova, Ekaterina
Maegdefessel, Lars
author_sort Eken, Suzanne M.
collection PubMed
description The rapid rise of type II diabetes mellitus and its accompanying vascular complications call for novel approaches in unravelling its pathophysiological mechanisms and designing new treatment modalities. Noncoding RNAs represent a class of previously unknown molecular modulators of this disease. The most important features of diabetes-induced vascular disease, which include metabolic deregulation, increased oxidative stress, release of inflammatory mediators like adipokines, and pathologic changes in vascular cells, all are depicted and governed by a certain set of noncoding RNAs. While these mechanisms are being unravelled, new diagnostic and therapeutic opportunities to treat diabetes-induced vascular disease emerge.
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spelling pubmed-38635032013-12-25 Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction Eken, Suzanne M. Jin, Hong Chernogubova, Ekaterina Maegdefessel, Lars J Diabetes Res Review Article The rapid rise of type II diabetes mellitus and its accompanying vascular complications call for novel approaches in unravelling its pathophysiological mechanisms and designing new treatment modalities. Noncoding RNAs represent a class of previously unknown molecular modulators of this disease. The most important features of diabetes-induced vascular disease, which include metabolic deregulation, increased oxidative stress, release of inflammatory mediators like adipokines, and pathologic changes in vascular cells, all are depicted and governed by a certain set of noncoding RNAs. While these mechanisms are being unravelled, new diagnostic and therapeutic opportunities to treat diabetes-induced vascular disease emerge. Hindawi Publishing Corporation 2013 2013-11-27 /pmc/articles/PMC3863503/ /pubmed/24369540 http://dx.doi.org/10.1155/2013/834727 Text en Copyright © 2013 Suzanne M. Eken et al. 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
Eken, Suzanne M.
Jin, Hong
Chernogubova, Ekaterina
Maegdefessel, Lars
Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title_full Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title_fullStr Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title_full_unstemmed Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title_short Making Sense in Antisense: Therapeutic Potential of Noncoding RNAs in Diabetes-Induced Vascular Dysfunction
title_sort making sense in antisense: therapeutic potential of noncoding rnas in diabetes-induced vascular dysfunction
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863503/
https://www.ncbi.nlm.nih.gov/pubmed/24369540
http://dx.doi.org/10.1155/2013/834727
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