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利用计算模型筛选具有雌激素受体生物活性的化学物质。

Screening Chemicals for Estrogen Receptor Bioactivity Using a Computational Model.

机构信息

†U.S. EPA, Office of Chemical Safety and Pollution Prevention, Washington, D.C. 20004, United States.

‡U.S. EPA, Office of Research and Development, Research Triangle Park, North Carolina 27709, United States.

出版信息

Environ Sci Technol. 2015 Jul 21;49(14):8804-14. doi: 10.1021/acs.est.5b02641. Epub 2015 Jun 26.

Abstract

The U.S. Environmental Protection Agency (EPA) is considering high-throughput and computational methods to evaluate the endocrine bioactivity of environmental chemicals. Here we describe a multistep, performance-based validation of new methods and demonstrate that these new tools are sufficiently robust to be used in the Endocrine Disruptor Screening Program (EDSP). Results from 18 estrogen receptor (ER) ToxCast high-throughput screening assays were integrated into a computational model that can discriminate bioactivity from assay-specific interference and cytotoxicity. Model scores range from 0 (no activity) to 1 (bioactivity of 17β-estradiol). ToxCast ER model performance was evaluated for reference chemicals, as well as results of EDSP Tier 1 screening assays in current practice. The ToxCast ER model accuracy was 86% to 93% when compared to reference chemicals and predicted results of EDSP Tier 1 guideline and other uterotrophic studies with 84% to 100% accuracy. The performance of high-throughput assays and ToxCast ER model predictions demonstrates that these methods correctly identify active and inactive reference chemicals, provide a measure of relative ER bioactivity, and rapidly identify chemicals with potential endocrine bioactivities for additional screening and testing. EPA is accepting ToxCast ER model data for 1812 chemicals as alternatives for EDSP Tier 1 ER binding, ER transactivation, and uterotrophic assays.

摘要

美国环境保护署(EPA)正在考虑采用高通量和计算方法来评估环境化学物质的内分泌生物活性。在这里,我们描述了一种多步骤、基于性能的新方法验证,并证明这些新工具足够强大,可以在内分泌干扰物筛选计划(EDSP)中使用。将来自 18 种雌激素受体(ER)ToxCast 高通量筛选测定的结果整合到一个计算模型中,该模型可以区分生物活性与特定于测定的干扰和细胞毒性。模型得分范围从 0(无活性)到 1(17β-雌二醇的生物活性)。ToxCast ER 模型的性能针对参考化学品以及当前实践中 EDSP 第 1 层筛选测定的结果进行了评估。当与参考化学品进行比较时,ToxCast ER 模型的准确性为 86%至 93%,并且对 EDSP 第 1 层指导方针和其他子宫增重研究的预测结果的准确性为 84%至 100%。高通量测定和 ToxCast ER 模型预测的性能表明,这些方法可以正确识别活性和非活性参考化学品,提供相对 ER 生物活性的度量,并快速识别具有潜在内分泌生物活性的化学品,以进行进一步筛选和测试。EPA 正在接受 ToxCast ER 模型对 1812 种化学物质的数据,作为 EDSP 第 1 层 ER 结合、ER 转录激活和子宫增重测定的替代方法。

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