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作 者:谢闺娥[1] 杜晶春[1] 董桂兰[2] 徐霞[1]
机构地区:[1]广州医科大学金域检验学院,广东广州510182 [2]广州大学门诊部,广东广州510006
出 处:《贵阳医学院学报》2016年第9期1029-1032,共4页Journal of Guiyang Medical College
基 金:国家自然科学基金(81101682);广东省公益研究与能力建设专项资金(2014A020212015)
摘 要:目的:研究扁蒴藤素对紫杉醇耐药乳腺癌细胞MCF-7/TAX生长的作用。方法:以乳腺癌细胞株MCF-7为对照,同时制作紫杉醇耐药乳腺癌细胞MCF-7/TAX;在两组细胞中分别给与7种浓度(0.25、0.5、1、2.5、5、10和20μmol/L)扁蒴藤素或紫杉醇培养48 h,用MTT法检测药物对MCF-7和MCF-7/TAX细胞作用的半数抑制浓度(IC50)值,并计算MCF-7/TAX细胞对紫杉醇或扁蒴藤素的耐药指数(RI);同时用Annexin VFITC/PI染色观察扁蒴藤素作用后MCF-7/TAX凋亡细胞比例。结果:MCF-7/TAX对紫杉醇RI达19.39,而扁蒴藤素对MCF-7/TAX细胞的生长有高效抑制作用,且呈现明显的剂量依赖性,对其作用48 h的IC50为0.52μmol/L,MCF-7/TAX对扁蒴藤素的RI仅为0.88;扁蒴藤素作用后,Annexin V染色阳性的MCF-7/TAX细胞比例较对照明显升高。结论:扁蒴藤素能抵抗紫杉醇耐药乳腺癌细胞的耐药性,激活MCF-7/TAX细胞凋亡,对其生长发挥高效抑制作用。Objective: To investigate the effect of pristimerin on the growth of taxol-resistant breast cancer cells MCF-7/TAX. Methods: The breast cancer cell line MCF-7 was the control group, and the taxol-resistant breast cancer cells line MCF-7/TAX was the observation group. In two groups of cells were cultured in 7 kinds of concentrations (0.25, 0.5, 1, 2.5, 5, 10 and 20 tool/L) pristime- rin and paclitaxel for 48 h. MTT assay was used to detect half inhibition concentration (IC50) value of drug on MCF-7 and MCF-7/tax ceils, and resistance index (RI) of cells to paclitaxel or pristimerin were calculated. At the same time Annexin V-FITC/PI staining was adopted to observe changes of pro- portion of apoptotie cells after pristimerin involvement. Results: The resistance index of MCF-7/TAX ceils to paclitaxel was 19.39. After treatment with pristimerin for 48 h, MCF-7/TAX ceils displayed markedly growth inhibition in a dose-dependent manner, and ICS0 for 48 h was 0.52 μM. The resist- ance index of MCF-7/TAX cells to pristimerin was 0. 88. After treatment with pristimerin, the propor- tion of positive MCF-7/TAX cells of Annexin V-FITC/PI staining was significantly higher than that of the control group. Conclusion: Pristimerin can resist resistance to paclitaxel resistance to breast canc-er cells, activate apoptosis of MCF-7/TAX cells, thus effectively inhibit cancer cells growth.
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