Rao V N, Shao N, Ahmad M, Reddy E S
Department of Microbiology and Immunology, Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107-5541, USA.
Oncogene. 1996 Feb 1;12(3):523-8.
Recently, BRCA1, a familial breast and ovarian cancer susceptible gene has been cloned and shown to be either lost or mutated in families with breast and ovarian cancers. BRCA1 has been postulated to encode a tumor suppressor, a protein that acts as a negative regulator of tumor growth. We have characterized the BRCA1 gene products by Western blot and immunoprecipitation analysis in mouse and tumor cells. Multiple BRCA1 polypeptides of approximately 225, 185, 160, 145, 100, 52 and 38 kD were identified in these cells. BRCA1 proteins were found to be localized mainly in the nucleus of normal Rat1 cells and human breast cancer cells. In order to understand the role of BRCA1 in cell transformation, we have established a stable NIH3T3 cell line expressing BRCA1 antisense RNA. The inhibition of expression of endogenous BRCA1 protein was detected in NIH3T3 transfectants by Western blot analysis. The antisense BRCA1 expressing NIH3T3 cells showed accelerated growth rate, anchorage independent growth and tumorigenicity in nude mice unlike the parental and sense transfectants. These results provide the first direct biological evidence for the possible function of BRCA1 as a tumor suppressor gene.
最近,一种家族性乳腺癌和卵巢癌易感基因BRCA1已被克隆,并且发现在患有乳腺癌和卵巢癌的家族中该基因要么缺失要么发生突变。BRCA1被推测编码一种肿瘤抑制因子,即一种作为肿瘤生长负调节因子的蛋白质。我们已通过蛋白质免疫印迹法和免疫沉淀分析在小鼠和肿瘤细胞中对BRCA1基因产物进行了表征。在这些细胞中鉴定出了多种分子量约为225、185、160、145、100、52和38千道尔顿的BRCA1多肽。发现BRCA1蛋白主要定位于正常大鼠1细胞和人乳腺癌细胞的细胞核中。为了了解BRCA1在细胞转化中的作用,我们建立了一个表达BRCA1反义RNA的稳定的NIH3T3细胞系。通过蛋白质免疫印迹分析在NIH3T3转染细胞中检测到内源性BRCA1蛋白表达受到抑制。与亲代细胞和正义转染细胞不同,表达反义BRCA1的NIH3T3细胞在裸鼠中显示出加速的生长速度、不依赖贴壁生长和致瘤性。这些结果为BRCA1作为肿瘤抑制基因的可能功能提供了首个直接的生物学证据。