Department of Pathology, Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts, USA.
Cancer Res. 2010 Feb 1;70(3):996-1005. doi: 10.1158/0008-5472.CAN-09-2842. Epub 2010 Jan 26.
BRCA1, the breast cancer- and ovarian cancer-specific tumor suppressor, can be a transcriptional repressor or a transcriptional activator, depending on the promoter context. To identify the genes activated or repressed by BRCA1, we have analyzed microarray results from cells depleted of BRCA1 and revealed a number of genes regulated by BRCA1 on the level of transcription. Among the genes repressed by BRCA1, we have identified amphiregulin (AREG) and early growth response-1 (EGR1). Results indicate that BRCA1 regulates AREG transcription directly through binding to the AREG promoter, however, we could not detect BRCA1 on the EGR1 promoter, suggesting that EGR1 is indirectly regulated by BRCA1. In an attempt to identify the mechanism of the AREG transcriptional repression by BRCA1, we have mapped two independent BRCA1 response elements on the AREG located at positions -202/-182 and +19/+122. BRCA1 depletion leads to induction of the AREG protein. Taken together, our data build the connection between BRCA1 loss of function and AREG upregulation-a change in gene expression often observed in breast cancer.
BRCA1 是一种乳腺癌和卵巢癌特异性肿瘤抑制因子,它可以作为转录抑制剂或转录激活剂,具体取决于启动子的上下文。为了确定 BRCA1 激活或抑制的基因,我们分析了 BRCA1 缺失细胞的微阵列结果,并揭示了许多受 BRCA1 转录水平调控的基因。在被 BRCA1 抑制的基因中,我们鉴定出了 Amphiregulin(AREG)和早期生长反应因子-1(EGR1)。结果表明,BRCA1 通过与 AREG 启动子结合直接调节 AREG 转录,但是,我们无法在 EGR1 启动子上检测到 BRCA1,这表明 EGR1 是由 BRCA1 间接调节的。为了试图确定 BRCA1 对 AREG 转录抑制的机制,我们在位于 -202/-182 和 +19/+122 位置的 AREG 上定位了两个独立的 BRCA1 反应元件。BRCA1 缺失会导致 AREG 蛋白的诱导。总之,我们的数据将 BRCA1 功能丧失与 AREG 上调联系起来——这是乳腺癌中经常观察到的基因表达变化。