Role and therapeutic potential of microRNAs in diabetes.

Détails

ID Serval
serval:BIB_4107378202ED
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Role and therapeutic potential of microRNAs in diabetes.
Périodique
Diabetes, Obesity & Metabolism
Auteur⸱e⸱s
Kolfschoten I.G., Roggli E., Nesca V., Regazzi R.
ISSN
1463-1326[electronic]
Statut éditorial
Publié
Date de publication
2009
Volume
11
Numéro
Suppl. 4
Pages
118-129
Langue
anglais
Résumé
The discovery in mammalian cells of hundreds of small RNA molecules, called microRNAs, with the potential to modulate the expression of the majority of the protein-coding genes has revolutionized many areas of biomedical research, including the diabetes field. MicroRNAs function as translational repressors and are emerging as key regulators of most, if not all, physiological processes. Moreover, alterations in the level or function of microRNAs are associated with an increasing number of diseases. Here, we describe the mechanisms governing the biogenesis and activities of microRNAs. We present evidence for the involvement of microRNAs in diabetes mellitus, by outlining the contribution of these small RNA molecules in the control of pancreatic beta-cell functions and by reviewing recent studies reporting changes in microRNA expression in tissues isolated from diabetes animal models. MicroRNAs hold great potential as therapeutic targets. We describe the strategies developed for the delivery of molecules mimicking or blocking the function of these tiny regulators of gene expression in living animals. In addition, because changes in serum microRNA profiles have been shown to occur in association with different human diseases, we also discuss the potential use of microRNAs as blood biomarkers for prevention and management of diabetes.
Mots-clé
Diabetes, Gene expression, Insulin, Pancreatic islet, Rma, Pancreatic beta-cells, Messenger-rnas, Systematic identification, Adipocyte differentiation, Insulin-secretion, Human cancer, C. Elegans, In-vivo, Expression, Targets
Pubmed
Web of science
Open Access
Oui
Création de la notice
29/10/2009 10:42
Dernière modification de la notice
20/08/2019 14:40
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