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The activation of melanogenesis by p-CREB and MITF signaling with extremely low-frequency electromagnetic fields on B16F10 melanoma

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dc.contributor.authorKim, Yu-Mi-
dc.contributor.authorCho, Sang-Eun-
dc.contributor.authorSeo, Young-Kwon-
dc.date.accessioned2024-08-08T01:02:10Z-
dc.date.available2024-08-08T01:02:10Z-
dc.date.issued2016-10-01-
dc.identifier.issn0024-3205-
dc.identifier.issn1879-0631-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/14928-
dc.description.abstractMelanin in the skin determines the skin color, and decreased melanin causes many hypopigmentation disorders and increased damage to skin by ultraviolet B (UVB) light irradiation. Here, we stimulate melanogenesis in B16F10 melanoma cells by using specific frequencies of ELF-EMFs. In this study, we focus on the melanogenesis of EMF-ELFs and find that 60-75 Hz ELF-EMFs upregulate melanin synthesis by stimulated expression of tyrosinase and TRP-1 through inhibition of phosphorylation ERK, activation of CREB, and MITF up-regulation in B16F10 melanoma cells. The results show that 60-75 Hz ELF-EMFs significantly increase secreted melanin, cellular melanin content, and tyrosinase activity, and the cell mitochondria activity, cell viability, and cell membrane condition are unchanged. Furthermore, the protein expression level of MITF and p-CREB signaling pathway are significantly increased. Moreover, 60 Hz ELF-EMFs reduce the phosphorylate of ERK in B16F10 melanoma cells. These findings indicate that stimulation of melanogenesis by using ELF-EMFs has therapeutic potential for treating hypopigmentation disorders such as vitiligo. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleThe activation of melanogenesis by p-CREB and MITF signaling with extremely low-frequency electromagnetic fields on B16F10 melanoma-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.lfs.2016.08.015-
dc.identifier.scopusid2-s2.0-84984633264-
dc.identifier.wosid000384632100004-
dc.identifier.bibliographicCitationLIFE SCIENCES, v.162, pp 25 - 32-
dc.citation.titleLIFE SCIENCES-
dc.citation.volume162-
dc.citation.startPage25-
dc.citation.endPage32-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
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.keywordPlusMESENCHYMAL STEM-CELLS-
dc.subject.keywordPlusERK ACTIVATION-
dc.subject.keywordPlusNEURAL DIFFERENTIATION-
dc.subject.keywordPlusALPHA-MSH-
dc.subject.keywordPlusTYROSINASE-
dc.subject.keywordPlusEXPOSURE-
dc.subject.keywordPlusEXTRACT-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROMOTER-
dc.subject.keywordAuthorExtremely low-frequency electromagnetic fields (ELF-EMFs)-
dc.subject.keywordAuthorMelanogenesis-
dc.subject.keywordAuthorp-CREB-
dc.subject.keywordAuthorMITF-
dc.subject.keywordAuthorB16F10 melanoma-
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