Azorsa D O, Cunliffe H E, Meltzer P S
Cancer Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, MD 20892-4470, USA.
Breast Cancer Res Treat. 2001 Nov;70(2):89-101. doi: 10.1023/a:1012972808558.
The steroid receptor coactivator AIB1 (amplified in breast cancer-1) is a transcriptional coactivator which has been found to be amplified in breast cancer. We have now investigated the role of the AIB1 protein in breast cancer cell lines. Although detectable levels of AIB1 were present in most cell lines, high levels of AIB1 expression were observed only in the ER-positive cell lines MCF-7 and BT-474 by western blot analysis. Newly developed monoclonal antibodies (mAbs) were used in several assays to show an association between AIBI and estrogen receptor-alpha (ER). AIB1 and ER co-localized to the nucleus of ER positive cell lines as shown by immunofluorescence microscopy, and a functional association of native AIB1 and ER in MCF-7 nuclear extracts was shown by EMSA. Recombinant ER also recruited AIB1 protein from nuclear extracts, shown by EMSA and by precipitation of ER-complex proteins bound to a biotinylated-ERE DNA target. Additionally, anti-AIB1 mAbs were able to immunoprecipitate ER from nuclear extracts of chemically cross-linked cells but not from uncross-linked cells. Both immunoprecipitation and oligonucleotide precipitation studies demonstrated the presence of p300 and CBP as part of the ER transcriptional complex. These results suggest that AIB1 and ER do associate physically in ER-positive breast cancer cell lines. We propose that in AIB1 amplified breast cancers, a heightened AIB1/ER association may play a crucial role in the progression of these tumors.
类固醇受体辅激活因子AIB1(乳腺癌-1中扩增)是一种转录辅激活因子,已发现其在乳腺癌中发生扩增。我们现在研究了AIB1蛋白在乳腺癌细胞系中的作用。虽然在大多数细胞系中都能检测到AIB1水平,但通过蛋白质免疫印迹分析仅在雌激素受体(ER)阳性细胞系MCF-7和BT-474中观察到高水平的AIB1表达。新开发的单克隆抗体(mAb)用于多项检测,以显示AIB1与雌激素受体α(ER)之间的关联。免疫荧光显微镜显示,AIB1和ER共定位于ER阳性细胞系的细胞核,电泳迁移率变动分析(EMSA)显示MCF-7核提取物中天然AIB1与ER存在功能关联。EMSA以及与生物素化雌激素反应元件(ERE)DNA靶点结合的ER复合蛋白沉淀结果表明,重组ER也从核提取物中募集AIB1蛋白。此外,抗AIB1 mAb能够从化学交联细胞的核提取物中免疫沉淀ER,但不能从未交联细胞中免疫沉淀ER。免疫沉淀和寡核苷酸沉淀研究均表明,p300和CBP作为ER转录复合物的一部分存在。这些结果表明,在ER阳性乳腺癌细胞系中,AIB1与ER确实存在物理关联。我们提出,在AIB1扩增的乳腺癌中,增强的AIB1/ER关联可能在这些肿瘤的进展中起关键作用。