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将邻苯二甲酸二(2-乙基)己酯映射到人类女性生殖毒性的不良结局途径网络中。

Mapping DEHP to the adverse outcome pathway network for human female reproductive toxicity.

机构信息

Department of Biology and Ecology, Faculty of Sciences, University of Novi Sad, Trg Dositeja Obradovica 2, 21000, Novi Sad, Serbia.

出版信息

Arch Toxicol. 2022 Oct;96(10):2799-2813. doi: 10.1007/s00204-022-03333-y. Epub 2022 Jul 5.

Abstract

Adverse outcome pathways (AOPs) and AOP networks are tools for mechanistic presentation of toxicological effects across different levels of biological organization. These tools are used to better understand how chemicals impact human health. In this study, a four-step workflow was used to derive the AOP network of human female reproductive toxicity (HFRT-AOP) from five AOPs available in the AOP-Wiki and ten AOPs obtained from the literature. Standard network analysis identified key events (KEs) that are point of convergence and divergence, upstream and downstream KEs, and bottlenecks across the network. To map di-(2-ethylhexyl) phthalate (DEHP) to the HFRT-AOP network, we extracted DEHP target genes and proteins from the Comparative Toxicogenomic and the CompTox Chemicals Dashboard databases. Enriched GO terms analysis was used to identify relevant biological processes in the ovary that are DEHP targets, whereas screening of scientific literature was performed manually and automatically using AOP-helpFinder. We combined this information to map DEHP to HFRT-AOP network to provide insight on the KEs and system-level perturbations caused by this endocrine disruptor and the emergent paths. This approach can enable better understanding of the toxic mechanism of DEHP-induced human female reproductive toxicity and reveal potential novel DEHP female reproductive targets for experimental studies.

摘要

不良结局途径 (AOPs) 和 AOP 网络是在不同层次的生物组织中呈现毒理学效应的机制工具。这些工具用于更好地了解化学物质如何影响人类健康。在这项研究中,使用四步工作流程从 AOP-Wiki 中提供的五个 AOP 和文献中获得的十个 AOP 中得出人类雌性生殖毒性 (HFRT-AOP) 的 AOP 网络。标准网络分析确定了关键事件 (KEs),这些 KEs 是汇聚和发散的点、上游和下游 KEs 以及网络中的瓶颈。为了将邻苯二甲酸二-(2-乙基己基)酯 (DEHP) 映射到 HFRT-AOP 网络,我们从比较毒理学基因组学和 CompTox 化学物质仪表板数据库中提取 DEHP 靶基因和蛋白质。使用富集的 GO 术语分析来识别卵巢中 DEHP 靶标相关的生物学过程,而使用 AOP-helpFinder 手动和自动筛选科学文献。我们将这些信息结合起来,将 DEHP 映射到 HFRT-AOP 网络,以了解这种内分泌干扰物引起的关键事件和系统水平扰动以及新兴路径。这种方法可以更好地理解 DEHP 诱导的人类雌性生殖毒性的毒性机制,并揭示潜在的新的 DEHP 雌性生殖靶标,用于实验研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/562c/9352620/32282ac9d079/204_2022_3333_Fig1_HTML.jpg

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