Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.
KMID : 0352720110350010086
Journal of Ginseng Research
2011 Volume.35 No. 1 p.86 ~ p.91
Ginsenoside F1 Modulates Cellular Responses of Skin Melanoma Cells
Yoo Dae-Sung

Rho Ho-Sik
Lee Yong-Gyu
Yeom Myung-Hun
Kim Duck-Hee
Lee Sang-Jin
Hong Sung-Youl
Lee Jae-Hwi
Cho Jae-Youl
Abstract
Ginsenoside (G)-F1 is an enzymatic metabolite generated from G-Rg1. Although this metabolite has been reported to suppress platelet aggregation and to reduce gap junction-mediated intercellular communication, the modulatory activity of G-F1 on the functional role of skin-derived cells has not yet been elucidated. In this study, we evaluated the regulatory role of G-F1 on the cellular responses of B16 melanoma cells. G-F1 strongly suppressed the proliferation of B16 cells up to 60% at 200 ¥ìg/mL, while only diminishing the viability of HEK293 cells up to 30%. Furthermore, G-F1 remarkably induced morphological change and clustering of B16 melanoma cells. The melanin production of B16 cells was also significantly blocked by G-F1 up to 70%. Interestingly, intracellular signaling events involved in cell proliferation, migration, and morphological change were up-regulated at 1 h incubation but down-regulated at 12 h. Therefore, our results suggest that G-F1 can be applied as a novel anti?skin cancer drug with anti-proliferative and anti-migration features.
KEYWORD
Panax ginseng, Ginsenoside F1, Experimental melanoma, Proliferation, Morphological change, Melanin production
FullTexts / Linksout information
Listed journal information
ÇмúÁøÈïÀç´Ü(KCI)