Inhibition of c-Kit signaling by diosmetin isolated from Chrysanthemum morifolium

The interaction of stem cell factor (SCF) with its cognate receptor c-Kit is closely associated with the survival and maturation of melanocytes. To investigate novel depigmentation agents, we screened 2,000 plant extracts for c-Kit inhibitors to identify active small molecules by using time-resolved...

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Published inArchives of pharmacal research Vol. 37; no. 2; pp. 175 - 185
Main Authors Lee, Seong Jin, Jung, Tae-Hoon, Kim, Hojeong, Jeong, Daeyoung, Choi, Gildon, Park, Woo-Kyu, Kong, Jae Yang, Jin, Mu-Hyun, Cho, Heeyeong
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.02.2014
대한약학회
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ISSN0253-6269
1976-3786
1976-3786
DOI10.1007/s12272-013-0158-7

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Summary:The interaction of stem cell factor (SCF) with its cognate receptor c-Kit is closely associated with the survival and maturation of melanocytes. To investigate novel depigmentation agents, we screened 2,000 plant extracts for c-Kit inhibitors to identify active small molecules by using time-resolved fluorescence enzyme assays. For the active extracts identified as inhibitors of c-Kit enzyme, we evaluated the effects of the active extracts and isolated flavonoids on c-Kit phosphorylation in MO7e/melanocytes. Anti-melanogenic activity was also examined in melanocytes and melanoderm model. The flavonoids such as diosmetin, apigenin, acacetin and luteolin isolated from Chrysanthemum morifolium were found to be active in inhibiting c-Kit both at enzyme and cellular levels. In addition, these flavonoids attenuated SCF-induced proliferation of human primary melanocytes without toxicity and suppressed ultraviolet (UV) B irradiation-mediated melanin synthesis significantly. Among the active flavonoids, diosmetin was found to inhibit SCF-induced melanogenesis in a human melanoderm model. These results strongly suggest that C. morifolium extract and diosmetin have potential to suppress SCF-/UVB-induced melanogenesis, and could be developed as anti-pigmentation agents.
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G704-000010.2014.37.2.015
ISSN:0253-6269
1976-3786
1976-3786
DOI:10.1007/s12272-013-0158-7