The potential of sestrins as therapeutic targets for diabetes

dc.contributor.authorDong, X. Charlie
dc.contributor.departmentDepartment of Biochemistry & Molecular Biology, IU School of Medicineen_US
dc.date.accessioned2017-06-08T14:00:30Z
dc.date.available2017-06-08T14:00:30Z
dc.date.issued2015-08
dc.description.abstractSestrins (Sesn1/2/3) belong to a small protein family that has versatile biological functions. In addition to initially characterized oxidoreductase activity, sestrins also have oxidoreductase-independent functions, including activation of AMP-activated protein kinase, inhibition of the mechanistic target of rapamycin complex 1 (mTORC1) and activation of mTORC2. As these kinases are important for metabolic regulation, sestrins have a favorable profile as potential therapeutic targets for metabolic diseases such as diabetes. Recent data are in line with such a notion. In this editorial, I have attempted to provide a brief update on the major findings in regard to sestrins in metabolism.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationDong, X. C. (2015). The Potential of Sestrins as Therapeutic Targets for Diabetes. Expert Opinion on Therapeutic Targets, 19(8), 1011–1015. http://doi.org/10.1517/14728222.2015.1044976en_US
dc.identifier.urihttps://hdl.handle.net/1805/12911
dc.language.isoen_USen_US
dc.publisherTaylor & Francisen_US
dc.relation.isversionof10.1517/14728222.2015.1044976en_US
dc.relation.journalExpert Opinion on Therapeutic Targetsen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourcePMCen_US
dc.subjectMechanistic target of rapamycin complex 1en_US
dc.subjectMechanistic target of rapamycin complex 2en_US
dc.subjectSestrinen_US
dc.subjectV-akt murine thymoma viral oncogene homologen_US
dc.titleThe potential of sestrins as therapeutic targets for diabetesen_US
dc.typeArticleen_US
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