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作 者:刘传亮[1] 王辉[2] 陈伟娟[3] 王晓杰[3] 李洪利[4] 赵修世[3] 李文通[3]
机构地区:[1]潍坊市人民医院保健三科 [2]潍坊医学院药理学教研室 [3]潍坊医学院病理学教研室 [4]潍坊医学院医学中心实验室,山东潍坊261041
出 处:《中国药理学通报》2010年第1期87-90,共4页Chinese Pharmacological Bulletin
基 金:山东省自然科学基金资助项目(NoY2008C75)
摘 要:目的探讨乳腺癌细胞中Snail过表达与P-gp之间的关系,揭示EMT对乳腺癌细胞多药耐药的影响。方法构建Snail真核表达载体pCDNA3.1-Snail,将载体转染人乳腺癌细胞MCF-7后用阿霉素对细胞进行诱导。利用细胞毒性实验(MTT)、阿霉素外排实验对耐药细胞系的耐药状况进行评价;通过流式细胞术和Real-time PCR分别测量耐药细胞系中P-gp和MDR1 mRNA,Snail mRNA的表达。结果由细胞毒性实验和阿霉素外排实验的结果显示,MCF-7/Snail细胞经阿霉素诱导后相对耐药指数升高至109.2,细胞内荧光强度降至7.1(P<0.05);Real-time PCR显示相对于MCF-7,MCF-7/Snail细胞中的MDR1 mRNA,Snail mRNA的表达明显升高与流式细胞术显示的P-gp升高相一致。结论转染Snail真核表达载体后,MCF-7/Snail细胞的耐药性较MCF-7细胞明显升高。Aim To explore the relationship between Snail and P-gp in breast cancer cell,and to reveal the effect of epithelial-mesenchymal transformation(EMT) on the multidrug-resistance ( MDR) of breast cancer cell. Methods The eukaryotic expression vector pCD-NA3. 1-Snail was constructed,and then transfected into human breast cancer cell line MCF-7 to constuct MCF-7 /Snail. Both cell lines MCF-7 and MCF-7/Snail were induced by adriamycin( ADM). Cell cytotoxicity assay and ADM efflux assay were used to measure the ability of drug resistance. The positive rate of P-gp of the two cell lines was detected by flow cytometry;the mRNA of MDR1 and Snail was evaluated by real-time PCR. Results MCF-7,the expression of MDR1 mRNA and Snail mRNA in MCF-7/Snail cell lines significantly increased;the expression of P-gp was increased too; the RR increased to 109. 2;fluorescence intensity intra-cellular was reduced to 7. 1. Conclusion After transfected the eukaryotic expression vector,the capacity of MCF-7/Snail strongly increases compared with that of MCF-7.
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