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dc.contributor.authorAlexander, Ryan
dc.contributor.authorLodish, Harvey F.
dc.contributor.authorSun, Lei
dc.date.accessioned2014-02-07T20:13:53Z
dc.date.available2014-02-07T20:13:53Z
dc.date.issued2011-02
dc.identifier.issn1472-8222
dc.identifier.issn1744-7631
dc.identifier.urihttp://hdl.handle.net/1721.1/84704
dc.descriptionavailable in PMC 2011 October 7en_US
dc.description.abstractIntroduction: Obesity and obesity-related disease have reached pandemic proportions and are prevalent even in developing countries. Adipose tissue is increasingly being recognized as a key regulator of whole-body energy homeostasis and consequently as a prime therapeutic target for metabolic syndrome. This review discusses the roles of miRNAs, small endogenously expressed RNAs that regulate gene expression at a post-transcriptional level, in the development and function of adipose tissue and other relevant metabolic tissues impacted by obesity. Several high-throughput studies have identified hundreds of miRNAs that are differentially expressed during the development of metabolic tissues or as an indication of pathophysiology. Further investigation has functionalized the regulatory capacity of individual miRNAs and revealed putative targets for these miRNAs. Therefore, as with several other pathologies, miRNAs are emerging as feasible therapeutic targets for metabolic syndrome. Areas covered: This review provides a comprehensive view of miRNAs involved in adipogenesis, from mesenchymal stem cell lineage determination through terminal adipocyte differentiation. We also discuss the differential expression of miRNAs among adipose depots and the dysregulation of miRNAs in other metabolic tissues during metabolic pathophysiology. Finally, we discuss the therapeutic potential of targeting miRNAs in obesity and give a perspective on the challenges and advantages of miRNA-based drugs. Expert opinion: miRNAs are extensive regulators of adipocyte development and function and are viable therapeutic targets for obesity. Despite the broad-spectrum and redundancy of miRNA–target interactions, sophisticated bioinformatic approaches are making it possible to determine the most physiologically relevant miRNAs to target in disease. In vivo delivery of miRNAs for therapeutic purposes is rapidly developing and has been successful in other contexts. Additionally, miRNAs can be used as prognosis markers for disease onset and progression. Ultimately, miRNAs are prime therapeutic targets for obesity and its consequent pathologies in other metabolic tissues.en_US
dc.language.isoen_US
dc.publisherInforma Healthcareen_US
dc.relation.isversionofhttp://dx.doi.org/10.1517/14728222.2011.561317en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleMicroRNAs in adipogenesis and as therapeutic targets for obesityen_US
dc.typeArticleen_US
dc.identifier.citationAlexander, Ryan, Harvey Lodish, and Lei Sun. “MicroRNAs in adipogenesis and as therapeutic targets for obesity.” Expert Opinion on Therapeutic Targets (February 28, 2011): 1-14.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorAlexander, Ryanen_US
dc.contributor.mitauthorLodish, Harvey F.en_US
dc.contributor.mitauthorSun, Leien_US
dc.relation.journalExpert Opinion on Therapeutic Targetsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsAlexander, Ryan; Lodish, Harvey; Sun, Leien_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7029-7415
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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