Planas-Silva M D, Shang Y, Donaher J L, Brown M, Weinberg R A
Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Cancer Res. 2001 May 15;61(10):3858-62.
AIB1 was isolated as a gene amplified in breast cancer and encodes a protein that acts as a steroid receptor coactivator. The role of steroid receptor coactivators such as AIB1 in breast cancer development is not clear. It is possible that AIB1 cooperates with estrogen receptor alpha in regulating estrogen-dependent cell proliferation. Ectopic expression of the estrogen receptor alpha in different cell lines does not confer estrogen-induced proliferation. This inability of the estrogen receptor to drive proliferation has been recently correlated with a lack of estrogen-dependent cyclin D1 expression in cells engineered to express the estrogen receptor. In this study, we evaluated whether high levels of AIB1 enable the estrogen receptor to direct the transcription of cyclin D1. We show here that AIB1 and other steroid receptor coactivators can enhance the functional interaction of the estrogen receptor with the cyclin D1 promoter. Increases of AIB1 levels in breast cancer cells by amplification and/or overexpression may represent one way to confer estrogen-dependent mitogenic stimulation to breast cancer cells.
AIB1最初是作为在乳腺癌中扩增的基因被分离出来的,它编码一种作为类固醇受体共激活因子的蛋白质。像AIB1这样的类固醇受体共激活因子在乳腺癌发展中的作用尚不清楚。AIB1有可能与雌激素受体α协同调节雌激素依赖性细胞增殖。在不同细胞系中异位表达雌激素受体α并不会赋予雌激素诱导的增殖能力。雌激素受体无法驱动增殖这一现象最近与在经过基因工程改造以表达雌激素受体的细胞中缺乏雌激素依赖性细胞周期蛋白D1的表达有关。在本研究中,我们评估了高水平的AIB1是否能使雌激素受体指导细胞周期蛋白D1的转录。我们在此表明,AIB1和其他类固醇受体共激活因子可以增强雌激素受体与细胞周期蛋白D1启动子的功能相互作用。通过扩增和/或过表达增加乳腺癌细胞中AIB1的水平可能是赋予乳腺癌细胞雌激素依赖性促有丝分裂刺激的一种方式。