Ginsenoside-Rg5 induces apoptosis and DNA damage in human cervical cancer cells

被引:97
作者
Liang, Li-Dan [1 ]
He, Tao [1 ]
Du, Ting-Wei [1 ]
Fan, Yong-Gang [1 ]
Chen, Dian-Sen [1 ]
Wang, Yan [1 ]
机构
[1] Henan Univ Sci & Technol, Affiliated Hosp 1, Dept Obstet & Gynecol, Luoyang 471003, Henan, Peoples R China
关键词
cervical cancer; ginsenoside-Rg5; DNA damage; apoptosis; TRADITIONAL CHINESE MEDICINE; SK-HEP-1; CELLS; BREAST-CANCER; COMET ASSAY; GINSENG; DEATH; RG5; MITOCHONDRIA; MANAGEMENT; MICE;
D O I
10.3892/mmr.2014.2821
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Panax ginseng is traditionally used as a remedy for cancer, inflammation, stress and aging, and ginsenoside-Rg5 is a major bioactive constituent of steamed ginseng. The present study aimed to evaluate whether ginsenoside-Rg5 had any marked cytotoxic, apoptotic or DNA-damaging effects in human cervical cancer cells. Five human cervical cancer cell lines (He La, MS751, C33A, Me180 and HT-3) were used to investigate the cytotoxicity of ginsenoside-Rg5 using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Additionally, the effects of ginsenoside-Rg5 on the apoptosis of He La and MS751 cells were detected using DNA ladder assays and flow cytometry. DNA damage was assessed in the He La and MS751 cells using alkaline comet assays and by detection of gamma H2AX focus formation. The He La and MS751 cells were significantly more sensitive to ginsenoside-Rg5 treatment compared with the C-33A, HT-3 and Me180 cells. As expected, ginsenoside-Rg5 induced significant concentration- and time-dependent increases in apoptosis. In addition, ginsenoside-Rg5 induced significant concentration-dependent increases in the level of DNA damage compared with the negative control. Consistent with the comet assay data, the percentage of gamma H2AX-positive He La and MS751 cells also revealed that ginsenoside-Rg5 caused DNA double-strands to break in a concentration-dependent manner. In conclusion, ginsenoside-Rg5 had marked genotoxic effects in the He La and MS751 cells and, thus, demonstrates potential as a genotoxic or cytotoxic drug for the treatment of cervical cancer.
引用
收藏
页码:940 / 946
页数:7
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