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作 者:谭波宇[1] 韦鸿雁[1] 陈丽[1] 刘文[1] 邓楠[1] TAN Bo-vu, WEI Hone-van, CHEN Li,et al.(The First Affiliated Hospital of Hunan Normal University,Hunan Provincial People's Hospital, Changsha 410002, China)
机构地区:[1]湖南师范大学附属第一医院,湖南省人民医院药学部
出 处:《中国肿瘤》2018年第4期316-320,共5页China Cancer
基 金:湖南省药学会科研资助项目生物专项(xy2015007)
摘 要:[目的]探讨人血清白蛋白(HSA)联用顺铂(DDP)对MCF7细胞耐药的影响。[方法]不同浓度DDP干预MCF7细胞72h,CCK8检验细胞增殖抑制率。选用DDP的IC50浓度分别与10、20μmol/L HSA联用,进一步检测联合用药对MCF7细胞的增殖抑制率。样品分为空白对照组、顺铂组、HSA组、顺铂联合HSA治疗组(10或20μmol/L)。各组处理MCF7细胞72h,实时荧光定量PCR(q RT-PCR)和免疫印迹法检测ERCC1 mRNA和蛋白表达。[结果]DDP联用10或20μmol/L HSA对MCF7的增殖抑制率分别为(50.97±1.50)%、(45.15±2.10)%,单独用药组DDP对MCF7的增殖抑制率为(55.60±5.20)%。q RT-PCR和Western blot检测表明DDP联用HSA(20μmol/L)显著增强ERCC1 m RNA和蛋白的表达。[结论 ]DDP联合使用高浓度HSA可通过上调ERCC1表达诱导化疗药物耐药。[Purpose] To investigate the effect of human serum albumin(HSA)combined with cisplatin(DDP)on the resistance of MCF7 cells. [Methods] MCF7 cells were intervened with DDP at different concentrations,and the inhibition rate of cell proliferation was examined by CCK8 after72 h treatment. The IC50 concentration of DDP was selected to be combined with 10 or 20μmol/L HSA respectively,and the inhibition rate of MCF7 cell proliferation by combined administration was further detected. The samples were divided into blank control group,DDP group,HSA group,DDP combined with HAS(10 or 20μmol/L)treatment group. Each group treated MCF7 cells for72 h and the expression of ERCC1 were detected by real-time quantitative PCR(q RT-PCR)and Western blot. [Results] DDP combined with 10 or 20 umol/L HSA on MCF7 proliferation inhibition rate were(50.97±1.50)% and(45.15±2.10)% respectively. The inhibition rate of DDP alone was(55.60±5.20)%. q RT-PCR and Western blot assays showed that DDP combined with HSA(20μmol/L)significantly enhanced ERCC1 m RNA and protein expression. [Conclusion] DDP combined with high concentration of HSA can induce resistance to chemotherapeutic drugs by upregulation of ERCC1 expression.
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