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Cited 16 time in webofscience Cited 18 time in scopus
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Inhibitory effect of cucurbitacin B on imiquimod-induced skin inflammation

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dc.contributor.authorLi, Zheng Jun-
dc.contributor.authorShin, Jung-Min-
dc.contributor.authorChoi, Dae-Kyoung-
dc.contributor.authorLim, Seul Ki-
dc.contributor.authorYoon, Tae-Jin-
dc.contributor.authorLee, Young Ho-
dc.contributor.authorSohn, Kyung-Cheol-
dc.contributor.authorIm, Myung-
dc.contributor.authorLee, Young-
dc.contributor.authorSeo, Young-Joon-
dc.contributor.authorKim, Chang Deok-
dc.contributor.authorLee, Jeung-Hoon-
dc.date.accessioned2022-12-26T21:47:02Z-
dc.date.available2022-12-26T21:47:02Z-
dc.date.issued2015-04-17-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/17294-
dc.description.abstractPsoriasis is a common skin disease, of which pathogenesis involves the increase of inflammatory reaction in epidermal cells. In an attempt to find therapeutics for psoriasis, we found that cucurbitacin B has an inhibitory potential on imiquimod-induced inflammation of keratinocytes. Cucurbitacin B significantly inhibited imiquimod-induced expression of crucial psoriatic cytokines, such as IL-8 and CCL20, via down-regulation of NF-kappa B and STAT3 signaling pathway in human keratinocytes. In addition, keratinocyte proliferation was markedly inhibited by cucurbitacin B. The potential beneficial effect of cucurbitacin B on psoriasis was further validated in imiquimod-induced psoriasiform dermatitis of experimental animal. Topical application of cucurbitacin B resulted in significant reduction of epidermal hyperplasia and inflammatory cytokines production, and ameliorated the psoriatic symptom. Taken together, these results suggest that cucurbitacin B may be a potential candidate for the treatment of psoriasis. (C) 2015 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleInhibitory effect of cucurbitacin B on imiquimod-induced skin inflammation-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2015.03.001-
dc.identifier.scopusid2-s2.0-84930702940-
dc.identifier.wosid000352922200019-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.459, no.4, pp 673 - 678-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume459-
dc.citation.number4-
dc.citation.startPage673-
dc.citation.endPage678-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusTOLL-LIKE RECEPTORS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusINNATE IMMUNITY-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusPSORIASIS-
dc.subject.keywordPlusKERATINOCYTES-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusDEFENSE-
dc.subject.keywordAuthorCucurbitacin B-
dc.subject.keywordAuthorImiquimod-
dc.subject.keywordAuthorKeratinocytes-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorSTAT3-
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