CHI Yu-gang,ZHONG Ling,WU Xia,WANG Yong.Grape seed proanthocyanidin extract inhibits proliferation and promotes apoptosis of ovary cancer cell line SKOV3[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(23):2203-2206.
CHI Yu-gang,ZHONG Ling,WU Xia,WANG Yong.Grape seed proanthocyanidin extract inhibits proliferation and promotes apoptosis of ovary cancer cell line SKOV3[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(23):2203-2206.DOI:
Western blot检测SKOV3细胞survivin在蛋白水平的表达。 结果 不同浓度(25、50、100、200、400 μg/ml)原花青素对SKOV3细胞作用48 h 的细胞增殖抑制率分别为48.67%、53.85%、67.03%、73.78%、77.39%。流式细胞和TUNEL检测经25 μg/ml原花青素处理24、48 h后SKOV3细胞凋亡率分别为31.98%、45.78%。葡萄籽原花青素还可以明显降低survivin的mRNA和蛋白水平的表达。这些作用均随原花青素浓度和作用时间的延长而增强。 结论 原花青素可能通过降低survivin的表达,在体外抑制SKOV3细胞增殖,并促进其凋亡。
Abstract
Objective To study the biological effects of grape seed proanthocyanidin extract (GSPE) on human ovary cancer cells and to explore the molecular mechanism. Methods Human ovary cancer cell line SKOV3 were co-cultured with GSPE solution of the terminal concentrations of 25
50
100
200
400 μg/ml respectively in 96-well plate. At 24
48
72 h after coculture
the following parameters were detected: cell growth curve
the inhibition rate of SKOV3 cells by MTT assay
DNA cycle by FCM
the apoptosis of SKOV3 by TUNEL and Annexin-V labeling method
the mRNA and protein expressions of survivin by semi-quantitative RT-PCR and Western blotting
respectively. Results GSPE dose-dependently inhibited the proliferation of the SKOV3 cells. Treated by GSPE
the progress of SKOV3 cells at S stage into G/M stage was inhibited. TUNEL showed that treated by 25 μg/ml GSPE for 24
48 h
the apoptotic rates of SKOV3 cells were 31.98%
45.78% respectively. Annexin-V showed that after incubation with 25 μg/ml GSPE for 24 h
the apoptotic rate was 14.68%. The survivin mRNA and protein expressions were both down-regulated. Conclusion GSPE inhibits the proliferation of malignant human ovary cancer cells and induces their apoptosis. Expression of survivin mRNA and protein may be related to cell growth inhibition and to the apoptosis mediated by GSPE in vitro.