Department of Pharmacology and Experimental Therapeutics, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.
Toxicol Lett. 2010 Dec 15;199(3):261-8. doi: 10.1016/j.toxlet.2010.09.008. Epub 2010 Sep 22.
Humans are chronically exposed to the plasticizer, Bisphenol A (BPA), that can adversely affect the normal hormonal regulation of cellular functions by mimicking the actions of estrogen. This biological response to BPA may vary according to an individual's genetic characteristics (e.g., BRCA1 mutations or deletion). In this study, both cell culture and mouse models were used to elucidate whether the loss of BRCA1 function could affect BPA-mediated cell proliferation. In studies using BPA levels comparable to human exposures, we found that loss of BRCA1 enhances BPA-induced cell proliferation in both systems. In vitro, we found that loss of BRCA1 enhances BPA-induced ERα signaling. In vivo, we found that BPA administration stimulates mammary gland epithelial tissue/cell proliferation leading to hyperplasia in Brca1 mutant mice compared to wild-type control mice. These results suggest that the biological responses in BRCA1-deficient cells may depend on environmental exposures, specifically BPA.
人类长期接触塑化剂双酚 A(BPA),BPA 可以通过模拟雌激素的作用,对细胞功能的正常激素调节产生不利影响。这种对 BPA 的生物学反应可能因个体的遗传特征(例如,BRCA1 突变或缺失)而异。在这项研究中,使用细胞培养和小鼠模型来阐明 BRCA1 功能的丧失是否会影响 BPA 介导的细胞增殖。在使用与人类暴露相当的 BPA 水平的研究中,我们发现 BRCA1 的缺失增强了这两个系统中 BPA 诱导的细胞增殖。在体外,我们发现 BRCA1 的缺失增强了 BPA 诱导的 ERα 信号。在体内,我们发现 BPA 给药刺激乳腺上皮组织/细胞增殖,导致 Brca1 突变小鼠的增生与野生型对照小鼠相比。这些结果表明,BRCA1 缺陷细胞中的生物学反应可能取决于环境暴露,特别是 BPA。