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dc.contributor.authorMacKenzie, Louise Susan
dc.contributor.authorLione, Lisa
dc.date.accessioned2013-12-17T08:30:17Z
dc.date.available2013-12-17T08:30:17Z
dc.date.issued2013-12
dc.identifier.citationMacKenzie , L S & Lione , L 2013 , ' Harnessing the benefits of PPARβ/δ agonists ' , Life Sciences , vol. 93 , no. 25-26 , pp. 963-967 . https://doi.org/10.1016/j.lfs.2013.10.022
dc.identifier.issn0024-3205
dc.identifier.urihttp://hdl.handle.net/2299/12350
dc.description.abstractLipid mediators have complex effects on the cell; one of the key transcriptional factors that moderate proliferation and inflammatory effects is PPARβ/δ. Following highly successful clinical trials using the PPARβ/δ agonists GW501516 for treatment of diabetes, GSK announced that any further research would be discontinued due to preclinical trials in rodents which linked this drug to wide spread tumour development. In this review we outline the dual molecular functions of PPARβ/δ and connect these to the diverse results from in vitro studies, and draw parallels with the outcomes of animal and human studies. The PPARβ/δ agonists have a great potential in terms of therapy, and we hope to provide some insight into the reasons why such contrasting results have been published. The discussion presented here is important to the future development of PPARβ/δ agonists for the clinic, and for a fuller understanding for their complex regulatory roles in the cell.en
dc.format.extent339036
dc.language.isoeng
dc.relation.ispartofLife Sciences
dc.titleHarnessing the benefits of PPARβ/δ agonistsen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.contributor.institutionDepartment of Human and Environmental Sciences
dc.contributor.institutionPharmacology and Clinical Science Research
dc.contributor.institutionAgriculture, Food and Veterinary Sciences
dc.contributor.institutionCardiovascular Pathologies
dc.contributor.institutionDiabetic neuropathies
dc.contributor.institutionTRP Ion channels
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionBasic and Clinical Science Unit
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1016/j.lfs.2013.10.022
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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