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作 者:郭银霞[1] 曾位森[1] 刘亚伟[2] 李煜生[2] 林俊[1] 熊静波[1] 罗深秋[1]
机构地区:[1]南方医科大学细胞生物学教研室,广东广州510515 [2]南方医科大学病理生理学教研室,广东广州510515
出 处:《南方医科大学学报》2008年第7期1157-1160,1164,共5页Journal of Southern Medical University
基 金:国家自然科学基金(30470673);广东省自然科学基金(040203064)~~
摘 要:目的研究BRCA1能否在乳腺癌细胞中调节黄体酮受体A和B的表达。方法在乳腺癌细胞MCF-7中,用lipofectamine 2000转染含有野生型BRCA1 cDNA的pFlag-CMV2-BRCA1 wt质粒或BRCA1特异性的小干扰RNA,过表达BRCA1或敲低BRCA1的表达。转染24h以后,加入含有100 nmol/L黄体酮完全培养基刺激24h。提取全细胞蛋白或总RNA,进行Western blotting和RT-PCR检测BRCA1、黄体酮受体A(PRA)和黄体酮受体B(PRB)在蛋白质水平和mRNA水平的表达。结果在MCF-7细胞中过表达BRCA1,PRA和PRB蛋白的表达下降,而PRA和PRB在mRNA水平无变化;BRCA1的表达被敲低后,PRA和PRB的表达升高。结论在乳腺癌细胞中,外源性和内源性BRCA1都可以下调PRA和PRB蛋白的表达。Objective To study the regulatory role of BRCAI in the expression of progesterone receptors A and B (PRA and PRB) in breast cancer cells. Methods Breast cancer MCF-7 cells were transfected with pFIag-CMV2-BRCA1 wt plasmid containing a full-length BRCAI cDNA or with BRCA1-specific siRNA via lipofectamine 2000 to induce overexpression or suppressed expression of BRCA1, respectively. Twenty-four hours after the transfection, the cells were incubated in flesh culture medium containing 100 nmol/L progesterone for 24 h. The total RNA extract or whole cell lysate was prepared for detecting BRCAI, PRA and PRB expressions using RT-PCR and Western blotting. Results The protein expressions of PRA and PRB were significantly decreased whereas their mRNA expressions remained unchanged in MCF-7 cells overexpressing BRCAI. In MCF-7 cells with BRCA1 knock-down, in contrast, the PRA and PRB protein expressions were markedly increased. Conclusion In breast cancer cells, exogenous and endogenous BRCA1 can both down-regulate the expressions of PRA and PRB at the protein level.
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