非那雄胺
小眼畸形相关转录因子
酪氨酸酶
黑色素
黑素皮质素1受体
黑素细胞
腺苷酸激酶
化学
黑素皮质素
内分泌学
黑色素瘤
内科学
癌症研究
药理学
生物
受体
激素
酶
前列腺
生物化学
医学
癌症
基因
等位基因
作者
Jae Ok Seo,Silvia Yumnam,Kwang Won Jeong,Sun Yeou Kim
标识
DOI:10.1007/s12272-018-1002-x
摘要
Finasteride is a well-known 5α-reductase inhibitor used for treatment of alopecia and prostate cancer. But the effect of finasteride in regulating melanogenesis is still unclear. In the present study the role of finasteride on melanogenesis was investigated. Finasteride decrease melanin level in melanocyte melan-a cells and B16F10 melanoma cells without inducing cytotoxicity. MC1R (melanocortin 1 receptor) protein expression was also inhibited by finasteride thereby decreasing the expression of adenylate cyclase, MITF (Melanogenesis associated transcription factor), tyrosinases, TRP (tyrosinase-related protein) -1 and -2. Thus our study suggest that finasteride inhibits melanogenesis in melanocyte and melanoma cells by inhibiting MC1R.
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