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Finasteride inhibits melanogenesis through regulation of the adenylate cyclase in melanocytes and melanoma cells

Authors
Seo, Jae OkYumnam, SilviaJeong, Kwang WonKim, Sun Yeou
Issue Date
Mar-2018
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
Finasteride; Melan-a; B16F10; MC1R; Melanogenesis
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.41, no.3, pp.324 - 332
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
41
Number
3
Start Page
324
End Page
332
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3988
DOI
10.1007/s12272-018-1002-x
ISSN
0253-6269
Abstract
Finasteride is a well-known 5 alpha-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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