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机构地区:[1]广州医科大学病理教研室,广东广州510182
出 处:《现代肿瘤医学》2015年第2期162-165,共4页Journal of Modern Oncology
基 金:教育部博士点基金博导类课题(编号:20134423110001);广东省自然科学基金(编号:S2012010010181);广州市科技计划项目(编号:2014Y2-001 71);广州市教育系统创新学术团队项目(编号:13C06);广州市属高校科研项目(编号:2012C135)
摘 要:目的:研究肺癌细胞A549在顺铂(DDP)间歇性干预后肿瘤干细胞(CSC)标志物(CD133)和上皮细胞间质转化(EMT)标志物(E-cadherin、β-catenin、Vimentin和Fibronectin)表达的变化,探讨肺癌耐药和CSC及EMT之间的相关性。方法:应用CCK-8法检测A549细胞对DDP的敏感性,DDP IC50间歇性处理A549细胞,采用Western blot法检测CD133蛋白表达变化,RT-q PCR法测定A549细胞处理前后E-cadherin、β-catenin、Vimentin和Fibronectin mRNA的表达。结果:肺腺癌细胞A549经DDP间歇性干预后,CSC标记物CD133蛋白表达增高,E-cadherin和β-catenin mRNA的相对表达量均显著降低,Vimentin mRNA的相对表达量显著增高。结论:A549细胞经DDP间歇性干预后有CSC标志物的表达,并表现出EMT的特性。Objective:To observe the impacts of intermittent cisplatin (DDP) on expression of cancer stem cell marker(CD133) and EMT markers (E-cadherin,β-catenin,Vimentin and Fibronectin) in lung cancer A549 cell lines,and explore the correlations of drug resistance,cancer sternness and EMT.Methods:The drugs sensitivity of A549 cells to cisplatin was detected by CCK-8.A549 cells were treated with cisplatin IC5o using interval-inactivation methods,CD133 protein expression of A549 cells in pre-and post-chemotherapy was detected by Western blot,and the expression of E-cadherin,β-catenin,Vimentin and Fibronectin was detected by Real-time PCR.Results:After treatment with intermittent cisplatin,the expression of CD133 in A549 cells was significantly enhanced,the relative expression of E-cadherin,β-catenin mRNA was significantly decreased,while the relative expression of Vimentin mRNA was significantly increased.Conclusion:After interval treatment with cisplatin,there is expression of cancer stem cell markers in A549 cells,which exhibit characteristics of EMT.
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