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dc.contributor.authorGILMER, JOHNen
dc.contributor.authorMEDINA MARTIN, CARLOSen
dc.date.accessioned2015-02-16T16:14:49Z
dc.date.available2015-02-16T16:14:49Z
dc.date.issued2015en
dc.date.submitted2015en
dc.identifier.citationO'Sullivan S, Gilmer JF, Medina C, Matrix metalloproteinases in inflammatory bowel disease: an update, Mediators of Inflammation, 2015, 964131-en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractMatrix metalloproteinases (MMPs) are known to be upregulated in inflammatory bowel disease (IBD) and other inflammatory conditions, but while their involvement is clear, their role in many settings has yet to be determined. Studies of the involvement of MMPs in IBD since 2006 have revealed an array of immune and stromal cells which release the proteases in response to inflammatory cytokines and growth factors. Through digestion of the extracellular matrix and cleavage of bioactive proteins, a huge diversity of roles have been revealed for the MMPs in IBD, where they have been shown to regulate epithelial barrier function, immune response, angiogenesis, fibrosis, and wound healing. For this reason, MMPs have been recognised as potential biomarkers for disease activity in IBD and inhibition remains a huge area of interest. This review describes new roles of MMPs in the pathophysiology of IBD and suggests future directions for the development of treatment strategies in this condition.en
dc.format.extent964131en
dc.language.isoenen
dc.relation.ispartofseriesMediators of Inflammationen
dc.rightsYen
dc.subjectinflammatory cytokinesen
dc.subject.lcshinflammatory cytokinesen
dc.titleMatrix metalloproteinases in inflammatory bowel disease: an updateen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/gilmerjfen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/martinc2en
dc.identifier.rssinternalid97169en
dc.identifier.doihttp://dx.doi.org/10.1155/2015/964131en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeCanceren
dc.subject.TCDThemeImmunology, Inflammation & Infectionen
dc.identifier.urihttp://hdl.handle.net/2262/73229


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