Biology of PXR

dc.contributor.authorWang, Jing
dc.contributor.authorDai, Shu
dc.contributor.authorGuo, Yan
dc.contributor.authorXie, Wen
dc.contributor.authorZhai, Yonggong
dc.date.accessioned2014-11-27T12:41:07Z
dc.date.available2014-11-27T12:41:07Z
dc.date.issued2014-07-07
dc.description.abstractHormonal homeostasis is essential for a variety of physiological and pathological processes. Elimination and detoxification of xenobiotics, such as drugs introduced into the human body, could disrupt the balance of hormones due to the induction of drug metabolizing enzymes (DMEs) and transporters. Pregnane X receptor (PXR, NR1I2) functions as a master xenobiotic receptor involved in drug metabolism and drug-drug interactions by its coordinated transcriptional regulation of phase I and phase II DMEs and transporters. Recently, increasing evidences indicate that PXR can also mediate the endocrine disrupt or function and thus impact the integrity of the endocrine system. This review focuses primarily on the recent advances in our understanding of the function of PXR in glucocorticoid, mineralocorticoid, androgen and estrogen homeostasis. The elucidation of PXR-mediated drug-hormone interactions might have important therapeutic implications in dealing with hormone-dependent diseases and safety assessment of drugs.en
dc.identifier.issn1611-2156
dc.identifier.urihttp://hdl.handle.net/2003/33729
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-6707
dc.language.isoen
dc.relation.ispartofseriesEXCLI Journal ; Vol. 13, 2014en
dc.subjectPXRen
dc.subjecthormone homeostasisen
dc.subjectxenobiotic receptoren
dc.subjectdrug-hormone interactionsen
dc.subject.ddc610
dc.titleBiology of PXRen
dc.title.alternativeRole in drug-hormone interactionsen
dc.typeText
dc.type.publicationtypearticle
dcterms.accessRightsopen access
eldorado.dnb.zdberstkatid2132560-1

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