Fernandez S V, Russo J
Breast Cancer Research Laboratory, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Toxicol Pathol. 2010 Jan;38(1):110-22. doi: 10.1177/0192623309354108. Epub 2009 Nov 21.
There is growing concern that estrogenic environmental compounds that act as endocrine-disrupting chemicals might potentially have adverse effects on hormone-sensitive organs such as the breast. This concern is further fueled by evidence indicating that natural estrogens, specifically 17beta-estradiol, are important factors in the initiation and progression of breast cancer. We have developed an in vitro-in vivo model in which we have demonstrated the carcinogenicity of E2 in human breast epithelial cells MCF-10F. Hypermethylation of NRG1, STXBP6, BMP6, CSS3, SPRY1, and SNIP were found at different progression stages in this model. The use of this powerful and unique model has provided a tool for exploring whether bisphenol A and butyl benzyl phthalate have relevance in the initiation of breast cancer. These studies provide firsthand evidence that the natural estrogen 17beta-estradiol and xenoestrogenic substances like bisphenol A are able to induce neoplastic transformation in human breast epithelial cells.
人们越来越担心,作为内分泌干扰化学物质的环境雌激素化合物可能会对诸如乳房等激素敏感器官产生潜在的不利影响。有证据表明天然雌激素,特别是17β-雌二醇,是乳腺癌发生和发展的重要因素,这进一步加剧了人们的担忧。我们开发了一种体外-体内模型,在该模型中我们证明了E2在人乳腺上皮细胞MCF-10F中的致癌性。在该模型的不同进展阶段发现了NRG1、STXBP6、BMP6、CSS3、SPRY1和SNIP的高甲基化。使用这个强大而独特的模型为探索双酚A和邻苯二甲酸丁苄酯在乳腺癌发生中是否具有相关性提供了一个工具。这些研究提供了第一手证据,表明天然雌激素17β-雌二醇和双酚A等外源性雌激素物质能够诱导人乳腺上皮细胞发生肿瘤转化。