Premium
Melochia corchorifolia extract inhibits melanogenesis in B16F10 mouse melanoma cells via activation of the ERK signaling
Author(s) -
Yuan XingHua,
Tian YuDan,
Oh JangHee,
Bach Tran The,
Chung Jin Ho,
Jin ZheHu
Publication year - 2020
Publication title -
journal of cosmetic dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.626
H-Index - 44
eISSN - 1473-2165
pISSN - 1473-2130
DOI - 10.1111/jocd.13282
Subject(s) - microphthalmia associated transcription factor , tyrosinase , mapk/erk pathway , melanin , blot , signal transduction , chemistry , phosphorylation , viability assay , protein kinase b , protein kinase a , kinase , melanoma , microbiology and biotechnology , biochemistry , biology , cell , cancer research , enzyme , gene
Background Numerous researches have focused on discovering available inhibitors of melanogenesis from natural medicinal plants with stable efficacy and safety to resolve cutaneous hyperpigmentary problems. Melochia corchorifolia Linn. (MC) has been used as folk medicine to treat various diseases. However, the effect of MC on melanogenesis remains unknown. Aim In this study, we investigated the effect of MC extract on melanogenesis and its underlying mechanisms in B16F10 mouse melanoma cells. Methods B16F10 cells were treated with MC extract, and then, cell viability, melanin content, and tyrosinase activity were analyzed. The mRNA and protein expression of tyrosinase and microphthalmia‐associated transcription factor (MITF) were evaluated using real‐time quantitative polymerase chain reaction (RT‐qPCR) and Western blotting, respectively. Phosphorylated or total protein levels in MC extract‐induced signaling pathways were analyzed by Western blotting. Results Treatment of B16F10 cells with MC extract inhibited melanin synthesis and intracellular tyrosinase activity in a dose‐dependent manner with no cytotoxicity. Protein and mRNA expressions of tyrosinase and MITF were also significantly decreased by MC extract treatment. In addition, phosphorylated level of extracellular signal‐regulated kinase (ERK) was obviously increased by MC extract, but AKT pathway was not activated. Inhibited ERK phosphorylation by pretreatment with a selective ERK inhibitor PD98059 significantly reversed the decreased melanin content induced by treatment with MC extract in B16F10 cells. Conclusion MC extract inhibits melanogenesis in B16F10 mouse melanoma cells through suppression of MITF‐tyrosinase signaling pathway by ERK activation.