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dc.contributor.author이정한-
dc.date.accessioned2018-04-16T04:53:38Z-
dc.date.available2018-04-16T04:53:38Z-
dc.date.issued2012-03-
dc.identifier.citationInternational Urogynecology Journal, Vol.23, No.3 [2012], p349–355en_US
dc.identifier.issn0937-3462-
dc.identifier.urihttp://link.springer.com/article/10.1007%2Fs00192-011-1567-0-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/67895-
dc.description.abstractIntroduction and hypothesisWe hypothesize that the abnormal extracellular matrix (ECM) turnover in pelvic tissues of women with prolapse may be attenuated by raloxifene. We examine the effect of raloxifene on ECM protein expression in pelvic fibroblasts.MethodsPelvic fibroblasts were isolated from cases (N = 6) and controls (N = 3). Cells were treated with raloxifene. Dose–response analyses were performed by ANOVA. mRNA and protein expression of collagen I, III, MMPs, and TIMPs were determined by RT-PCR and Western blot. MMP activity was analyzed by zymography.ResultsThe mRNA expression of TIMP-3 and protein expression of TIMP-1 and TIMP-3 were significantly increased by raloxifene in fibroblasts from both cases and controls (P < 0.05). Collagen I, III, and MMP mRNA and protein expressions were not affected.ConclusionsRaloxifene selectively attenuates abnormal matrix degradation by increasing inhibitors of proteases, TIMPs, in pelvic fibroblasts. This opens the possibility for SERMs to be used as preventive therapy for pelvic floor disorders.en_US
dc.description.sponsorshipThis work was supported by the National Institute of Aging at the National Institutes of Health [RO1 AG01790] and the Mary Lake Polan Transition Fund of the Stanford University School of Medicine.en_US
dc.language.isoenen_US
dc.publisherSpringer Science + Business Mediaen_US
dc.subjectCollagenen_US
dc.subjectMMPen_US
dc.subjectPelvic organ prolapseen_US
dc.subjectRaloxifeneen_US
dc.subjectTIMPen_US
dc.subjectPelvic floor disorderen_US
dc.titleThe effect of raloxifene, a SERM, on extracellular matrix protein expression of pelvic fibroblastsen_US
dc.typeArticleen_US
dc.relation.no3-
dc.relation.volume23-
dc.identifier.doi10.1007/s00192-011-1567-0-
dc.relation.page349-355-
dc.relation.journalINTERNATIONAL UROGYNECOLOGY JOURNAL-
dc.contributor.googleauthorLee, J. H.-
dc.contributor.googleauthorWen, Y.-
dc.contributor.googleauthorPolan, M. L.-
dc.contributor.googleauthorChen, B.-
dc.relation.code2012213338-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidobgyleejh-
dc.identifier.researcherID36065969600-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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