为不良后果途径开发数据丰富的关键事件关系的方法,以雄激素受体活性降低与肛门距离缩短的关系为例。

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-07-08 DOI:10.1016/j.reprotox.2024.108662
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引用次数: 0

摘要

不良后果途径(AOP)框架作为一种辅助化学危害评估的工具,已被毒理学学科广泛接受。尽管 AOP 的开发活动日益活跃,但大量完全认可的 AOP 进展缓慢,部分原因是根据《AOP 开发者手册》构建完整的 AOP 是一项具有挑战性的任务。为了促进开源AOP-wiki平台吸收更多新的知识单元,最近提出了一种务实的方法。这种方法包括通过系统方法考虑关键事件关系 (KER),因为它们代表了基本的知识单元,可以从低复杂性测试数据中推断出完整生物体不良结果的因果关系。不过,最好能更广泛地采用统一的 KER 开发方法。以《AOP 开发者手册》为指导,我们开发了一种将 "雄激素受体(AR)活性降低 "与 "雌雄生殖器距离(AGD)缩短 "联系起来的 KER,以展示一种适用于未来开发需要系统文献检索方法的 KER 的方法。
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Methodology for developing data-rich Key Event Relationships for Adverse Outcome Pathways exemplified by linking decreased androgen receptor activity with decreased anogenital distance

The Adverse Outcome Pathway (AOP) framework has gained widespread acceptance in toxicological disciplines as a tool for aiding chemical hazard assessment. Despite increased activity in AOP development, progress towards a high volume of fully endorsed AOPs has been slow, partly due to the challenging task of constructing complete AOPs according to the AOP Developer’s Handbook. To facilitate greater uptake of new knowledge units onto the open-source AOP-wiki platform, a pragmatic approach was recently proposed. This approach involves considering Key Event Relationships (KERs) for individual development through systematic approaches, as they represent essential units of knowledge from which causality can be inferred; from low complexity test data to adverse outcomes in intact organisms. However, more broadly adopted harmonized methodologies for KER development would be desirable. Using the AOP Developer’s Handbook as a guide, a KER linking 'decreased androgen receptor (AR) activity' with 'reduced anogenital distance (AGD)' was developed to demonstrate a methodology applicable for future developments of KERs requiring systematic literature retrieval approaches.

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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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