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作 者:李玮妮[1] 陈立涵[1] 程龙[1] 付洁[1] 林亚红[1] 刘婕[1] 张浩[1] 叶棋浓[1]
机构地区:[1]军事医学科学院生物工程研究所,北京100850
出 处:《生物技术通讯》2013年第5期624-627,共4页Letters in Biotechnology
基 金:国家重点基础研究发展计划(2011CB504200);北京市自然科学基金(7112101)
摘 要:目的:建立稳定高表达雌激素受体β(ERβ)蛋白表达的乳腺癌ZR75-1细胞株,检测其对上皮细胞间质转化(EMT)相关基因的影响。方法:将编码人ERβ的cDNA序列插入慢病毒表达载体pCDH-EF1-MCS-T2A-Puro,将其与慢病毒包装辅助质粒共转染293T细胞后收集病毒上清,感染乳腺癌ZR75-1细胞,经嘌呤霉素筛选后获得稳定高表达含Myc标签的人ERβ的混合细胞集落,以及作为对照组整合有对照慢病毒载体pCDH-EF1-MCS-T2A-Puro的混合细胞集落,提取细胞蛋白,用Myc抗体检测Myc-ERβ融合蛋白的表达,同时检测EMT相关基因Snail、E-Cadherin、N-Cadherin的表达水平和GSK-3β的磷酸化水平。结果:建立了稳定高表达Myc-ERβ融合蛋白的乳腺癌细胞株,和对照组相比,Myc-ERβ高表达抑制EMT相关蛋白N-cadherin和Snail的表达,增强E-cadherin分子的表达,抑制GSK-3β磷酸化水平。结论:建立了Myc-ERβ高表达的乳腺癌细胞株,发现ERβ高表达抑制EMT相关分子的表达,为深入研究分子在乳腺癌中调控的机制奠定了基础。Objective: To construct a breast cancer ZR75-1 cell line stably overexpressing estrogen receptor β(ERβ)and detect its effects on the expression of epithelial-mesenchymal transition(EMT)associated genes. Methods: Cloning ERβ cDNA into the lentivirus vector pCDH-EF1-MCS-T2A-Puro,which was then packaged with accessary plasmids into lentivirus in 293T cells. After infected with lentivirus and selected by puromycin, mixed ZR75-1 colonies stably expressing Myc-ERβ were obtained and the fusion Myc-ERβ expression was detected by Western blot. Meanwhile, the expression of EMT associated protein such as Snail, E-Cadherin, N-Cadherin and GSK-3β in ERβ overexpression ZR75-1 cells was compared with that in vector control cells. Results: N-cadherin and Snail expression was decreased and E-cadherin increased in ERβ overexpressing cells, Moreover, ERβ overexpression may decrease the GSK-3β phophorylation level. Conclusion: Breast cancer cell line overexpression ERβ was successfully constructed and ERβ overexpression may regulate the expression of several protein involved in EMT, which has established a good foundation for further study of the mechanism of the regulation of EMT by ERβ in breast cancer cells.
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