机构地区:[1]Division of Life Science,Korea Basic Science Institute,Daejeon 305-333,Korea [2]East-West Cancer Center,Dunsan Oriental Hospital of Daejeon University,Daejeon 302-122,Korea [3]Graduate School of Analytical Science and Technology,Chungnam National University,Daejeon 305-764,Korea
出 处:《Chinese Journal of Integrative Medicine》2016年第5期344-352,共9页中国结合医学杂志(英文版)
基 金:financially supported bythe Korea Basic Science Institute grant(D33403);partly by University-Institute Cooperation Program grant of the National Research Foundation funded by the Korean Government(MEST)
摘 要:Objective: To investigate the effect of three major ginsenosides from mountain ginseng as anti- cancer substance and explore the underlying mechanism involved in lung cancer. Methods: The inhibitory proliferation of lung cancer by major five ginsenosides (Rbl, Rb2, Rgl, Rc, and Re) was examined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Calculated 50% inhibition (IC50) values of five ginsenosides were determined and compared each other. Apoptosis by the treatment of single ginsenoside was performed by fluorescence-assisted cytometric spectroscopy. The alterations of apoptosis-related proteins were evaluated by Western blot analysis. Results: The abundance of ginsenosides in butanol extract of mountain ginseng (BX-MG) was revealed in the order of Rbl, Rgl, Re, Rc and Rb2. Among them, Rbl was the most effective to lung cancer cell, followed by Rb2 and Rgl on the basis of relative IC50 values of IMR90 versus A549 cell. The alterations of apoptotic proteins were confirmed in lung cancer A549 cells according to the administration of Rbl, Rb2 and Rgl. The expression levels of caspase-3 and caspase-8 were increased upon the treatment of three ginsenosides, however, the levels of caspase-9 and anti-apoptotic protein Bax were not changed. Conclusion: Major ginsenosides such as Rbl, Rb2 and Rgl comprising BX-MG induced apoptosis in lung cancer cells via extrinsic apoptotic pathway rather than intrinsic mitochondrial pathway.Objective: To investigate the effect of three major ginsenosides from mountain ginseng as anti- cancer substance and explore the underlying mechanism involved in lung cancer. Methods: The inhibitory proliferation of lung cancer by major five ginsenosides (Rbl, Rb2, Rgl, Rc, and Re) was examined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Calculated 50% inhibition (IC50) values of five ginsenosides were determined and compared each other. Apoptosis by the treatment of single ginsenoside was performed by fluorescence-assisted cytometric spectroscopy. The alterations of apoptosis-related proteins were evaluated by Western blot analysis. Results: The abundance of ginsenosides in butanol extract of mountain ginseng (BX-MG) was revealed in the order of Rbl, Rgl, Re, Rc and Rb2. Among them, Rbl was the most effective to lung cancer cell, followed by Rb2 and Rgl on the basis of relative IC50 values of IMR90 versus A549 cell. The alterations of apoptotic proteins were confirmed in lung cancer A549 cells according to the administration of Rbl, Rb2 and Rgl. The expression levels of caspase-3 and caspase-8 were increased upon the treatment of three ginsenosides, however, the levels of caspase-9 and anti-apoptotic protein Bax were not changed. Conclusion: Major ginsenosides such as Rbl, Rb2 and Rgl comprising BX-MG induced apoptosis in lung cancer cells via extrinsic apoptotic pathway rather than intrinsic mitochondrial pathway.
关 键 词:Butanol extract of mountain ginseng ginsenoside lung cancer apoptosis
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