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dc.contributor.authorSun, Xiaoyan-
dc.contributor.authorKim, Yang-Hyun-
dc.contributor.authorTrong Nhat Phan-
dc.contributor.authorYang, Beom-Seok-
dc.date.accessioned2024-01-20T08:31:59Z-
dc.date.available2024-01-20T08:31:59Z-
dc.date.created2022-01-10-
dc.date.issued2014-11-02-
dc.identifier.issn0916-8451-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/126140-
dc.description.abstractBurn scar contracture that follows the healing of deep dermal burns causes severe deformation and functional impairment. However, its current therapeutic interventions are limited with unsatisfactory outcomes. When we treated deep second-degree burns in rat skin with activin-like kinase 5 (ALK5) inhibitor A-83-01, it reduced wound contraction and enhanced the area of re-epithelialization so that the overall time for wound closing was not altered. In addition, it reduced myofibroblast population in the dermis of burn scar with a diminished deposition of its biomarker proteins such as alpha-SMA and collagen. Treatment of rat dermal fibroblast with A-83-01 inhibited transforming growth factor-beta 1 (TGF-beta 1)-dependent induction of alpha-SMA and collagen type I. Taken together, these results suggest that topical application of ALK5 inhibitor A-83-01 could be effective in preventing the contraction of burn wound without delaying the wound closure by virtue of its inhibitory activity against the TGF-beta-induced increase of myofibroblast population.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectGROWTH-FACTOR-BETA-
dc.subjectMUSCLE ACTIN EXPRESSION-
dc.subjectI-RECEPTOR KINASE-
dc.subjectTGF-BETA-
dc.subjectSIGNALING PATHWAY-
dc.subjectBREAST-CANCER-
dc.subjectTISSUE-REPAIR-
dc.subjectFIBROSIS-
dc.subjectCELLS-
dc.subjectLUNG-
dc.titleTopical application of ALK5 inhibitor A-83-01 reduces burn wound contraction in rats by suppressing myofibroblast population-
dc.typeArticle-
dc.identifier.doi10.1080/09168451.2014.932666-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, v.78, no.11, pp.1805 - 1812-
dc.citation.titleBIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY-
dc.citation.volume78-
dc.citation.number11-
dc.citation.startPage1805-
dc.citation.endPage1812-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000343816500001-
dc.identifier.scopusid2-s2.0-84938524268-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.type.docTypeArticle-
dc.subject.keywordPlusGROWTH-FACTOR-BETA-
dc.subject.keywordPlusMUSCLE ACTIN EXPRESSION-
dc.subject.keywordPlusI-RECEPTOR KINASE-
dc.subject.keywordPlusTGF-BETA-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusTISSUE-REPAIR-
dc.subject.keywordPlusFIBROSIS-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusLUNG-
dc.subject.keywordAuthorALK5 inhibitor-
dc.subject.keywordAuthormyofibroblast-
dc.subject.keywordAuthorTGF-beta signaling-
dc.subject.keywordAuthorA-83-01-
dc.subject.keywordAuthorburn wound contraction-
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