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机构地区:[1]淮阴卫生高等职业技术学校,江苏淮安223300
出 处:《现代肿瘤医学》2014年第3期516-518,共3页Journal of Modern Oncology
基 金:淮安市科技基金项目(编号:2009002-4)
摘 要:目的:体外观察低剂量人参皂甙Rh2(ginsenoside Rh2,GS-Rh2)对抗肿瘤药顺铂(cisplatin,DDP)杀伤人食管癌细胞株Eca109的影响,并探讨其可能的作用机制。方法:人食管癌细胞Eca109经培养符合条件后,分别加用0.3μg/ml DDP(A组)、20μmol/ml GS-Rh2(B组)、0.3μg/ml DDP+20μmol/ml GS-Rh2(C组)、对照组(D组)处理48小时。流式细胞仪检测各组细胞凋亡率和死亡率。高效液相色谱检测各组细胞内DDP的药物浓度。蛋白质印迹法检测各组细胞中p53表达。结果:细胞凋亡率和死亡率C组显著高于A、B两组(P<0.05);C组细胞内DDP的药物浓度显著高于A组细胞(P<0.05);C组细胞p53表达水平低于A组(P<0.05)。结论:体外低剂量GS-Rh2能增强DDP对人食管癌细胞Eca109的杀伤作用,其作用机制可能与降低细胞内p53表达有关。Objective:To observe the effect of cisplatin on Eea109 cells by treatment with low dose of ginsenoside Rh2,and explore the preliminary mechanisms. Methods:The apoptosis was assayed by flow cytometry. HPLC was used to determine DDP. The expression of p53 was detected by Western blot. Results:The cell apoptosis and mortality in group C was significantly higher than A, B groups (P 〈 0.05). Drug concentration of DDP within cells in group C was significantly higher than A two groups (P 〈 0.05). But the p53 expression of group C was lower than A group (P 〈 0.05). Conclusion: Eca109 cells with GS - RH2 increased the killing effect of DDP,and the mechanism is related to inhibiting the expression of p53 glycoprotein inside the cells.
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