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Stimulation of melanogenesis by scoparone in B16 melanoma cells.

Stimulation of melanogenesis by scoparone in B16 melanoma cells. Research Abstract Details 

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  • Stimulation of melanogenesis by scoparone in B16 melanoma cells. Abstract Text:

    jeong-yeh yangJeong-yeh Yang,jeung-hyun kooJeung-hyun Koo,young-gil songYoung-gil Song,kang-beom kwonKang-beom Kwon,ju-hyung leeJu-hyung Lee,hee-sook sohnHee-sook Sohn,byung-hyun parkByung-hyun Park,eun-chung jheeEun-chung Jhee,jin-woo parkJin-woo Park,jeong-yeh yangJeong-yeh Yang,jeung-hyun kooJeung-hyun Koo,young-gil songYoung-gil Song,kang-beom kwonKang-beom Kwon,ju-hyung leeJu-hyung Lee,hee-sook sohnHee-sook Sohn,byung-hyun parkByung-hyun Park,eun-chung jheeEun-chung Jhee,jin-woo parkJin-woo Park,

    AIM: The effect of coumarin derivatives on melanogenesis was investigated in B16 murine melanoma cells. METHODS: Melanin content and tyrosinase activity were analyzed spectrophotometrically. The expression of tyrosinase, tyrosinase-related protein-1 (TRP-1) and tyrosinase-related protein-2 (TRP-2) were measured either by reverse transcription-polymerase chain reaction (RT-PCR) or Western blot. RESULTS: Among the coumarin derivatives studied, scoparone (6,7- dimethoxycoumarin) was the most potent; the 6- or 7-methoxy group was found to be essential for the stimulation of melanogenesis. The melanin content was greatly increased by scoparone in a dose-dependent manner; there was no cytotoxicity at the effective concentrations. Scoparone increased enzyme activity as well as protein and mRNA expression of tyrosinase. In addition, mRNA of TRP-1 and TRP-2 were also increased after treatment with scoparone. H-89, an inhibitor of protein kinase A (PKA), completely inhibited the scoparone-induced increase of melanogenesis and the tyrosinase protein. CONCLUSION: These results suggest that scoparone-induced stimulation of melanogenesis is likely to occur at the transcriptional level of melanogenesis-related enzymes through PKA signaling.

    Stimulation of melanogenesis by scoparone in B16 melanoma cells. Publishing Authors By Initials

    jy yangJY Yang,jh kooJH Koo,yg songYG Song,kb kwonKB Kwon,jh leeJH Lee,hs sohnHS Sohn,bh parkBH Park,ec jheeEC Jhee,jw parkJW Park,jy yangJY Yang,jh kooJH Koo,yg songYG Song,kb kwonKB Kwon,jh leeJH Lee,hs sohnHS Sohn,bh parkBH Park,ec jheeEC Jhee,jw parkJW Park,

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    PUBMED ID PMID:

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    Stimulation of melanogenesis by scoparone in B16 melanoma cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Acta pharmacologica Sinica

    VOLUME: 27

    Page Numbers: 1467-73

    Journal Abbreviation: Acta Pharmacol. Sin.

    ISSN: 1671-4083

    DAY: 19

    MONTH: Nov

    YEAR: 2006

    Stimulation of melanogenesis by scoparone in B16 melanoma cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100956087

    Stimulation of melanogenesis by scoparone in B16 melanoma cells. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Stimulation of melanogenesis by scoparone in B16 melanoma cells. Information

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    Grant and Affiliation Information for Stimulation of melanogenesis by scoparone in B16 melanoma cells.

    AFFILIATION: Department of Biochemistry, Dental School, Chonbuk National University, Jeonju 561-756, Korea.

    Country: China

    China Research PublicationChina Research Publication

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    MEDLINETA: Acta Pharmacol Sin

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