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Cited 13 time in webofscience Cited 13 time in scopus
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Inhibition of collagen synthesis by IWR-1 in normal and keloid-derived skin fibroblasts

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dc.contributor.authorZhou, Ming-Wei-
dc.contributor.authorYin, Wei-Tian-
dc.contributor.authorJiang, Ri-Hua-
dc.contributor.authorLee, Jin-Hyup-
dc.contributor.authorKim, Chang-Deok-
dc.contributor.authorLee, Jeung-Hoon-
dc.contributor.authorZhu, Ming Ji-
dc.contributor.authorYoon, Tae-Jin-
dc.date.accessioned2022-12-26T18:48:45Z-
dc.date.available2022-12-26T18:48:45Z-
dc.date.issued2017-03-15-
dc.identifier.issn0024-3205-
dc.identifier.issn1879-0631-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13816-
dc.description.abstractAims: Keloid is a benign tumor that is characterized by the hyperproliferation of dermal fibroblasts and excessive deposition of extracellular matrix (ECM) especially the collagen. Aberrant activation of Wnt/beta-catenin signaling is implicated in the pathogenesis of keloid. In this study, we investigated the effects of IWR-1, a small molecule inhibitor for Wnt/beta-catenin signaling via the inhibition of tankyrase, on production of collagen and matrix metalloproteinase (MMP) in dermal fibroblasts. Main methods: We cultured human normal skin- and keloid-derived fibroblasts, then treated with IWR-1. The effects of IWR-1 on collagen and MMP production were determined by Western blot, ELISA and zymography. Key findings: IWR-1 significantly suppressed the proliferation and migration of both the normal and keloid fibroblasts. IWR-1 also inhibited the production and secretion of type I collagen from the fibroblasts. In addition, IWR-1 significantly increased the expression of MMPs, such as MMP-1, MMP-3 and MMP-13, along with the increase of gelatinase activity. These results suggest that inhibitory effect of IWR-1 on collagen production may be related with the increased MMP activity. Significance: This study provides the possible action mechanism of IWR-1 on regulation of collagen expression, on which to base further investigation for preventing skin fibrotic diseases such as keloid. (C) 2016 Elsevier Inc. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleInhibition of collagen synthesis by IWR-1 in normal and keloid-derived skin fibroblasts-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.lfs.2016.12.003-
dc.identifier.scopusid2-s2.0-85013236890-
dc.identifier.wosid000397700900012-
dc.identifier.bibliographicCitationLIFE SCIENCES, v.173, pp 86 - 93-
dc.citation.titleLIFE SCIENCES-
dc.citation.volume173-
dc.citation.startPage86-
dc.citation.endPage93-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusEPITHELIAL-MESENCHYMAL TRANSITION-
dc.subject.keywordPlusTGF-BETA-
dc.subject.keywordPlusMATRIX METALLOPROTEINASES-
dc.subject.keywordPlusHYPERTROPHIC SCARS-
dc.subject.keywordPlusPULMONARY-FIBROSIS-
dc.subject.keywordPlusPROTEIN CBP-
dc.subject.keywordPlusCATENIN-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorCollagen-
dc.subject.keywordAuthorFibroblasts-
dc.subject.keywordAuthorIWR-1-
dc.subject.keywordAuthorKeloid-
dc.subject.keywordAuthorMatrix metalloproteinase-
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