Leidos, Research Triangle Park, NC, USA.
Center for Computational Toxicology and Exposure, U.S. Environmental Protection Agency, Research Triangle Park, NC, USA.
ALTEX. 2023;40(2):217–236. doi: 10.14573/altex.2202231. Epub 2022 Jun 23.
Evaluating chemicals for potential in vivo toxicity based on their in vitro bioactivity profile is an important step toward animal- free testing. A compendium of reference chemicals and data describing their bioactivity on specific molecular targets, cellular pathways, and biological processes is needed to bolster confidence in the predictive value of in vitro hazard detection. Endogenous signaling by all-trans retinoic acid (ATRA) is an important pathway in developmental processes and toxicities. Employing data extraction methods and advanced literature extraction tools, we assembled a set of candidate reference chemicals with demonstrated activity on ten protein family targets in the retinoid system. The compendium was culled from Protein Data Bank, ChEMBL, ToxCast/Tox21, and the biomedical literature in PubMed. Finally, we performed a case study on one chemical in our collection, citral, an inhibitor of endogenous ATRA production, to determine whether the literature supports an adverse outcome pathway explaining the compound’s developmental toxicity initiated by disruption of the retinoid pathway. We also deliver an updated Abstract Sifter tool populated with these reference compounds and complex search terms designed to query the literature for the downstream consequences to support concordance with targeted retinoid pathway disruption.
基于体外生物活性谱评估化学品的体内潜在毒性是实现无动物测试的重要步骤。需要编制参考化学品纲要,并提供描述其对特定分子靶标、细胞途径和生物过程的生物活性的数据,以增强对体外危害检测的预测价值的信心。全反式视黄酸 (ATRA) 的内源性信号传导是发育过程和毒性中的重要途径。我们采用数据提取方法和先进的文献提取工具,在视黄醇系统的十个蛋白家族靶标上汇集了一组具有活性的候选参考化学品。该纲要从蛋白数据库、ChEMBL、ToxCast/Tox21 和 PubMed 中的生物医学文献中筛选而来。最后,我们对我们收集的一种化学物质柠檬醛进行了案例研究,柠檬醛是内源性 ATRA 产生的抑制剂,以确定文献是否支持一种不良结局途径,解释该化合物通过破坏视黄醇途径引发的发育毒性。我们还提供了一个更新的 Abstract Sifter 工具,其中填充了这些参考化合物和复杂的搜索词,旨在查询文献以支持与靶向视黄醇途径破坏的一致性。