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作 者:邓菊庆[1] 刘金保[1] 温冠媚[1] 董伟华[1]
机构地区:[1]广州医学院病理生理学教研室,广州510182
出 处:《广州医学院学报》2010年第2期13-16,共4页Academic Journal of Guangzhou Medical College
基 金:国家自然科学基金(30770835);国家863计划项目(2006AA02Z4B5).
摘 要:目的:观察蛋白酶体抑制剂MG132联合使用3种化疗药物对人乳腺癌细胞MCF-7的抑制作用。方法:采用Alamar Blue^TM方法检测细胞的生长抑制效应。实验分4组:①化疗药物处理组(紫杉醇、紫苹素或阿霉素的不同浓度);②MG132组(1.25、2.5、5、10μmoL/L);③MG132联合3种化疗药物处理组;④溶剂对照组。MCF-7细胞分别使用上述药物处理40h后,加入Alamar Blue^TM孵育8h,测定OD值并计算细胞相对活力。结果:①MG1325μLmol/L及其以下浓度对MCF-7没有抑制效应;②3种化疗药物的不同浓度处理细胞后,细胞活力随药物的浓度升高明显下降,具有明显的剂量依赖效应;③选择MG1325μmol/L分别与3种化疗药物联合处理后,MCF-7细胞的活力明显下降,紫杉醇为19.10%、紫苹素19.13%,阿霉素27.17%,与化疗药物处理组比较差异有统计学意义(P〈0.05)。结论:蛋白酶体抑制剂MG132明显增强紫杉醇、紫草素和阿霉素对MCF-7细胞的抑制作用。Objective:To observe the inhibitory effects on human breast cancer cells (MCF-7) by proteasome inhibitor MG132 added to a triple-drug chemotherapy. Methods: AlamarBlueTM assay was used to detect the cell viability. MCF-7 cells ware randomly divided into four groups : chemotherapeutics treated group ( several concentrations of paclitaxel,shikonin or doxorubicin) , MGI32 treated group ( 1.25μmol/L,2.5μmol/L,5μmol/L and lOp.tool/L), MG132 plus chemotherapeuties group and solvent control group. After MCF-7 cells were treated for 40hrs, AlamarBlue^TM was added for 8 hours and the OD value was detected to calculate the relative viability of cells. Results: ①There was no significant inhibitory effect when MCF-7 cells were treated with MG132 at doses not higher than 5 μmol/L; ② Relative cell viability decreased significantly with increasing doses of 3 chemotherapeutics in an apparent dose-dependant manner;③Afier MCF-7 cells were concurrently treated with 5 μmol/L MG132 and chemotherapeutics, the relative cell viability was reduced dramatically (to 19.10% with paclitaxel, 19.13% with shikonin, and 27.17% with doxorubicin) ,compared with single use of chemotherapeutics (P 〈 0.05 ). Conclusion: The inhibitory effect of paclitaxel, shikonin and doxorubiein on MCF-7 cells was enhanced significantly by proteasome inhibitor MG132.
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