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作 者:肖集文[1] 庄英帜[1] 曹建国[2] 尹婵[1] 陈雪莲[1] 柳娜[1]
机构地区:[1]南华大学附属第一医院肿瘤科,湖南衡阳421001 [2]南华大学肿瘤研究所,湖南衡阳421001
出 处:《中华肿瘤防治杂志》2009年第3期175-178,共4页Chinese Journal of Cancer Prevention and Treatment
摘 要:目的:研究黄荆子提取物EVn-50对人乳腺癌MCF-7细胞生长抑制和凋亡的诱导作用。方法:在体外培养人乳腺癌MCF-7细胞,采用表柔比星、他莫西芬和不同浓度的EVn-50处理MCF-7细胞,软琼脂和平皿克隆法测定EVn-50抑制MCF-7细胞增殖的量-效关系,TUNEL法、流式细胞术分析其细胞凋亡率和周期分布。结果:EVn-50对MCF-7细胞增殖的抑制作用随药物浓度的提高而更加明显,而在低浓度时却表现出轻微促细胞增殖现象(<10.0μg/mL),100.0μg/mL时抑制率为48.68%,实验组与对照组比较,差异有统计学意义,P<0.01。TUNEL法和流式细胞术分析结果表明,高浓度的EVn-50能诱导MCF-7细胞凋亡,阻滞细胞于G2/M期,降低细胞增殖指数,且也存在量-效关系。结论:EVn-50在高浓度时可抑制人乳腺癌MCF-7细胞增殖并诱导其凋亡,具有明显的抗肿瘤作用。OBJECTIVE: To investigate the effects of Semen Viticis negundo extract (EVn 50) on cell proliferation and apoptosis of human breast cancer cell line MCF-7. METHODS: Human breast cancer cell line MCF-7 was treated with ADM, tamoxifen and different con centration of Semen Viticis negundo extract (EVn-50). The capacityactivity relationship of inhibit MCF-7 cell proliferation was detected by soft agar cloning and plate cloning formation assay. The rate of apop tosis and the distribution of cell cycle in MCF-7 cells were investigated by TUNEL and flow cytometry. RESULTS: Soft agar cloning and plate cloning formation assay showed that the proliferation of MCF-7 cells in vitro was inhibited by EVn-50 in concentration-dependent manners. But it could promote the proliferation in low concentration (〈10.0 μg/mL). and it was 48. 68 % when the density of EVn-50 was 100.0 μg/mL. It was found that there was a significant difference between the experiment groups and control group, P〈0.01. TUNEL method and flow cytometry analysis showed that high concentrations of EVn-50 can induce apoptosis in MCF-7 cells, the cell block at the G2/M phase, the lower the index of cell proliferation, and also the volumeactivity relationship. CONCLUSION: The Semen Viticis ne gundo extract (EVn 50) has the effect of anti tumor for it can inhibit the proliferation and induce the cell apoptosis of MCF-7 cells.
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