Post-Graduation Program in Biochemistry, Department of Biochemistry and Molecular Biology, Federal University of Ceará, Fortaleza, Brazil.
Department of Molecular Biology, Federal University of Paraíba, João Pessoa, Brazil.
Methods Mol Biol. 2024;2753:151-157. doi: 10.1007/978-1-0716-3625-1_6.
An Adverse Outcome Pathway (AOP) is an analytical model that describes, through a graphical representation, a linear sequence of biologically connected events at different levels of biological organization, causally leading to an adverse effect on human health or the environment. In general, AOPs are constructed based on five central principles: systematic development and review, chemical-agnostic, modular, networks, and living documents. Furthermore, AOPs have the potential to be used, for example, to investigate certain molecular targets; relate the regulation of specific genes or proteins among AOPs; extrapolate biological processes, pathways, or diseases from one species to another; and even predict adverse effects in particular populations. AOPs also emerge as an alternative to animal experimentation in studies of developmental malformations. It's even possible now to develop a quantitative AOP to predict teratogenic effects for some substances. However, the construction of high-quality AOPs requires standardization in the way these models are developed and reviewed, ensuring an adequate degree of flexibility and guaranteeing efficiency. The development of AOPs should strictly be based on the guidance documents developed by the OECD. Nevertheless, an important step for those developing AOPs is the choice of an apical endpoint or an initiating molecular event in order to initiate the construction of the pathway. Another crucial step is a systematic literature review based on the random combination of the blocks of information. With these two fundamental steps completed, it only remains to follow the guidance documents on Developing and Assessing Adverse Outcome Pathways and AOP Developers' Handbook supplement provided by the OECD to organize and construct an AOP. This modern approach will bring radical changes in the field of toxicity testing, regarding the prediction of apical toxic effects using molecular-level effects.
不良结局途径(AOP)是一种分析模型,通过图形表示,描述了不同生物组织层次上生物连接事件的线性序列,因果导致对人类健康或环境的不良影响。一般来说,AOP 是基于五个核心原则构建的:系统开发和审查、无化学偏见、模块化、网络和活文档。此外,AOP 有可能用于例如,研究某些分子靶标;将特定基因或蛋白质在 AOP 之间的调控联系起来;推断从一个物种到另一个物种的生物过程、途径或疾病;甚至预测特定人群中的不良影响。AOP 也在发育畸形研究中作为动物实验的替代方法出现。现在甚至有可能开发出一种定量 AOP 来预测某些物质的致畸作用。然而,高质量 AOP 的构建需要在这些模型的开发和审查方式上进行标准化,以确保足够的灵活性并保证效率。AOP 的开发应严格遵循 OECD 制定的指导文件。然而,对于那些开发 AOP 的人来说,一个重要的步骤是选择一个顶端终点或一个起始分子事件,以便开始构建途径。另一个关键步骤是基于信息块的随机组合进行系统的文献综述。完成这两个基本步骤后,只需遵循 OECD 提供的《开发和评估不良结局途径指南》和《AOP 开发者手册》补充件,即可组织和构建 AOP。这种现代方法将在毒性测试领域带来根本性的变化,即在使用分子水平的影响预测顶端毒性效应方面。