Induction of apoptosis by ginsenoside Rk1 in SK-MEL-2-human melanoma.

Abstract

Ginsenosides are active compounds isolated from Panax ginseng Meyer. Among these ginsenosides, less polar ginsenosides such as ginsenoside Rg3 and ginsenoside Rh2 have been demonstrated to have tumor inhibitory effects because of their cytotoxicity. In this study, we evaluated the apoptotic effects of ginsenoside Rk1 in SK-MEL-2 human melanoma. Ginsenoside Rk1 isolated from red ginseng is one of the novel ginsenosides that shows strong cytotoxicity compared to ginsenoside Rg3 in dose- and time-dependent manners. The results of DNA fragmentation, 4',6-diamidino-2-phenylindole staining, and flow cytometric analysis are corroborated that ginsenoside Rk1 induced apoptosis in SK-MEL-2 cells. Western blot analysis revealed up-regulation of Fas, FasL, and Bax protein expression and down-regulation of procaspase-8, procaspase-3, mutant p53 and Bcl-2 protein expression. These findings suggest that ginsenoside Rk1 might be a promising compound to induce apoptosis through both extrinsic and intrinsic pathways in SK-MEL-2 cells.

• Authors: Ji Seong Kim, Eun Ji Joo, Jaemoo Chun, Young Wan Ha, Jue-Hee Lee, Yongmoon Han, Yeong Shik Kim
• Journal: Archives of pharmacal research (Arch Pharm Res) Vol. 35 Issue 4 Pg. 717-22 (Mar 2012) ISSN: 1976-3786 [Electronic] Korea (South)
• PMID: 22553065 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents, Phytogenic
• FAS protein, human
• FASLG protein, human
• Fas Ligand Protein
• Ginsenosides
• Proto-Oncogene Proteins c-bcl-2
• fas Receptor
• ginsenoside Rk1

Topics

• Antineoplastic Agents, Phytogenic (chemistry, pharmacology)
• Apoptosis (drug effects)
• Blotting, Western
• Cell Culture Techniques
• Cell Line, Tumor
• Cell Survival (drug effects)
• DNA Fragmentation (drug effects)
• Dose-Response Relationship, Drug
• Fas Ligand Protein (biosynthesis)
• Flow Cytometry
• Ginsenosides (chemistry, pharmacology)
• Humans
• Melanoma (metabolism, pathology)
• Molecular Structure
• Proto-Oncogene Proteins c-bcl-2 (biosynthesis)
• Skin Neoplasms (metabolism, pathology)
• Time Factors
• Up-Regulation
• fas Receptor (biosynthesis)