摘要: |
目的观察山竹提取物(GME)对人胃癌细胞SGC-7901增殖情况的影响,探讨其作用机制。方法采用新型四氮唑盐法(MTS)检测GME对SGC-7901细胞增殖的影响;采用流式细胞仪检测GME对SGC-7901细胞凋亡和诱导活性氧(ROS)水平的影响;采用Westernblot检测不同浓度GME对BGC-7901细胞的PTEN、Bax、Bcl-2表达的影响。结果GME显著抑制SGC-7901细胞的增殖(P<0.05),与阳性对照组5-氟尿嘧啶(5-FU)相比抑制率也较高(P<0.05),其半数抑制浓度为:7.89滋g/ml。经5、7.5滋g/ml的GME处理24h后,可有效促进SGC-7901细胞凋亡(P<0.05),ROS水平的累积;GME相同方式处理后,SGC-7901细胞中PTEN和Bax的蛋白表达量上调,Bcl-2蛋白表达量降低(P<0.05)。结论GME能够显著抑制胃癌SGC-7901细胞的增殖,能够诱导SGC-7901细胞ROS水平的累积,并通过影响PTEN、Bax和Bcl-2蛋白的表达,促进其凋亡。 |
关键词: 山竹提取物 增殖 胃癌 SGC-7901 细胞 |
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基金项目:浙江省中医药优秀青年人才基金 |
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Effect of Garcinia mangostana extract on proliferation of gastric cancer SGC-7901 cells in vitro |
WANG Rongguo,LI Kaiqiang,ZHANG Zhijian,WANG Qiang
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Taizhou First People's Hospital
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Abstract: |
Objective To investigate the effect of Garcinia mangostana Extract (GME) on proliferation of gastric cancer SGC-7901 cells. Methods Human gastric cancer SGC-7901 cells were treated with 5滋g/ml and 7.5滋g/ml GME for 24h. SGC-7901 cell proliferation was determined by tetrazolium salt reduction method (MTS), cell apoptosis and reactive oxygen species (ROS) were measured by flow cytometry, PTEN, Bax and Bcl-2 protein expressions in SGC-7901 cells were detected by Western blot. Results GME significantly inhibited the proliferation of SGC-7901 cells(P<0.05) witha 50% inhibitory concentrations
of 7.89滋g/ml, the inhibition rate was higher than that of 5-fluorouracil (5-FU)(P<0.05). After treated with 5 μg/ml and 7.5滋g/ml of GME for 24h, apoptosis of SGC-7901 cells was increased (P<0.05 ), and the cell ROS levels was also increased; the expressions of PTEN and Bax proteins in SGC-7901 cells were increased, while Bcl-2 expression levels were reduced (P<0.05). Conclusion This study suggests that GME can significantly inhibit proliferation of SGC-7901 cells, enhance ROS levels, and promote apoptosis of SGC-7901 cells, which is associated with up-regulation of PTEN, Bax and down-regulation of Bcl-2 expression. |
Key words: Garcinia mangostana extract Proliferation Gastric cancer SGC-7901 cell line |