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Inhibitory effect of 5-iodotubercidin on pigmentation

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dc.contributor.authorKim, Kyung-Il-
dc.contributor.authorJeong, Hae Bong-
dc.contributor.authorRo, Hyunju-
dc.contributor.authorLee, Jeung-Hoon-
dc.contributor.authorKim, Chang Deok-
dc.contributor.authorYoon, Tae-Jin-
dc.date.accessioned2022-12-26T18:33:07Z-
dc.date.available2022-12-26T18:33:07Z-
dc.date.issued2017-09-02-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13486-
dc.description.abstractMelanin pigments are the primary contributors for the skin color. They are produced in melanocytes and then transferred to keratinocytes, eventually giving various colors on skin surface. Although many depigmenting and/or skin-lightening agents have been developed, there is still a growing demand on materials for reducing pigmentation. We attempted to find materials for depigmentation and/or skin lightening using the small molecule compounds commercially available, and found that 5-iodotubercidin had inhibitory potential on pigmentation. When HM3KO melanoma cells were treated with 5-iodotubercidin, pigmentation was dramatically reduced. The 5-iodotubercidin decreased the protein level for pigmentation-related molecules such as MITF, tyrosinase, and TRP1. In addition, 5-iodotubercidin decreased the phosphorylation of CREB, while increased the phosphorylation of ART and ERR. These data suggest that 5-iodotubercidin inhibits melanogenesis via the regulation of intracellular signaling related with pigmentation. Finally, 5-iodotubercidin markedly inhibited the melanogenesis of zebrafish embryos, an in vivo evaluation model for pigmentation. Together, these data suggest that 5-iodotubercidin can be developed as a depigmenting and/or skin-lightening agent. (C) 2017 Elsevier Inc. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleInhibitory effect of 5-iodotubercidin on pigmentation-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2017.07.008-
dc.identifier.scopusid2-s2.0-85021751258-
dc.identifier.wosid000407528800024-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.490, no.4, pp 1282 - 1286-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume490-
dc.citation.number4-
dc.citation.startPage1282-
dc.citation.endPage1286-
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.keywordPlusMELANOGENESIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusZEBRAFISH-
dc.subject.keywordPlusSKIN-
dc.subject.keywordPlusMELANOCYTES-
dc.subject.keywordPlusMELANOMA-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordAuthor5-lodotubercidin-
dc.subject.keywordAuthorPigmentation-
dc.subject.keywordAuthorCREB-
dc.subject.keywordAuthorAKT-
dc.subject.keywordAuthorERK-
dc.subject.keywordAuthorZebrafish-
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