文章基本信息

标题：Evaluation of Bisphenol A (BPA) Exposures on Prostate Stem Cell Homeostasis and Prostate Cancer Risk in the NCTR-Sprague-Dawley Rat: An NIEHS/FDA CLARITY-BPA Consortium Study
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作者：Gail S. Prins ; Wen-Yang Hu ; Lishi Xie 等
期刊名称：Environmental Health Perspectives
印刷版ISSN：0091-6765
电子版ISSN：1552-9924
出版年度：2018
卷号：126
期号：11
页码：117001
DOI：10.1289/EHP3953
语种：English
出版社：OCR Subscription Services Inc
摘要：Background: Previous work determined that early life exposure to low-dose Bisphenol A (BPA) increased rat prostate cancer risk with aging. Herein, we report on prostate-specific results from CLARITY-BPA (Consortium Linking Academic and Regulatory Insights on BPA Toxicity), which aims to resolve uncertainties regarding BPA toxicity. Objectives: We sought to a ) reassess whether a range of BPA exposures drives prostate pathology and/or alters prostatic susceptibility to hormonal carcinogenesis, and b ) test whether chronic low-dose BPA targets prostate epithelial stem and progenitor cells. Methods: Sprague-Dawley rats were gavaged daily with vehicle, ethinyl estradiol (EE) or 2.5 – 25,000 μ g BPA/kg-BW during development or chronically, and prostate pathology was assessed at one year. One developmentally exposed cohort was given testosterone plus estradiol ( T + E ) implants at day 90 to promote carcinogenesis with aging. Epithelial stem and progenitor cells were isolated by prostasphere (PS) culture from dorsolateral prostates (DLP) of rats continuously exposed for six months to 2.5 – 250 μ g BPA/kg-BW. Gene expression was analyzed by quantitative real time reverse transcription polymerase chain reaction (qRT-PCR). Results: Exposure to BPA alone at any dose did not drive prostate pathology. However, rats treated with EE, 2.5, 250, or 25,000 μ g BPA/kg-BW plus T + E showed greater severity of lateral prostate intraepithelial neoplasia (PIN), and DLP ductal adenocarcinoma multiplicity was markedly elevated in tumor-bearing rats exposed to 2.5 μ g BPA / kg -BW. DLP stem cells, assessed by PS number, doubled with chronic EE and 2.5 μ g BPA / kg -BW exposures. PS size, reflecting progenitor cell proliferation, was greater at 25 and 250 μ g BPA doses, which also shifted lineage commitment toward basal progenitors while reducing luminal progenitor cells. Conclusions: Together, these results confirm and extend previous evidence using a rat model and human prostate epithelial cells that low-dose BPA augments prostate cancer susceptibility and alters adult prostate stem cell homeostasis. Therefore, we propose that BPA exposures may contribute to the increased carcinogenic risk in humans that occurs with aging.