Section of Ecotoxicology and Risk Assessment , Norwegian Institute for Water Research (NIVA) , Gaustadalléen 21 , N-0349 Oslo , Norway.
Centre for Environmental Radioactivity (CERAD) , Norwegian University of Life Sciences (NMBU) , P.O. Box 5003, N-1432 Ås , Norway.
Environ Sci Technol. 2018 May 1;52(9):5479-5489. doi: 10.1021/acs.est.8b00749. Epub 2018 Apr 19.
The use of classical mixture toxicity models to predict the combined effects of environmental stressors based on toxicogenomics (OMICS) data is still in its infancy. Although several studies have made attempts to implement mixture modeling in OMICS analysis to understand the low-dose interactions of stressors, it is not clear how interactions occur at the molecular level and how results generated from such approaches can be better used to inform future studies and cumulative hazard assessment of multiple stressors. The present work was therefore conducted to propose a conceptual approach for combined effect assessment using global gene expression data, as illustrated by a case study on assessment of combined effects of gamma radiation and depleted uranium (DU) on Atlantic salmon ( Salmo salar). Implementation of the independent action (IA) model in reanalysis of a previously published microarray gene expression dataset was performed to describe gene expression patterns of combined effects and identify key gene sets and pathways that were relevant for understanding the interactive effects of these stressors. By using this approach, 3120 differentially expressed genes (DEGs) were found to display additive effects, whereas 279 (273 synergistic, 6 antagonistic) were found to deviate from additivity. Functional analysis further revealed that multiple toxicity pathways, such as oxidative stress responses, cell cycle regulation, lipid metabolism, and immune responses were enriched by DEGs showing synergistic gene expression. A key toxicity pathway of DNA damage leading to enhanced tumorigenesis signaling is highlighted and discussed in detail as an example of how to take advantage of the approach. Furthermore, a conceptual workflow describing the integration of combined effect modeling, OMICS analysis, and bioinformatics is proposed. The present study presents a conceptual framework for utilizing OMICS data in combined effect assessment and may provide novel strategies for dealing with data analysis and interpretation of molecular responses of multiple stressors.
基于毒理学基因组学(OMICS)数据,使用经典混合物毒性模型预测环境胁迫物综合效应的方法仍处于起步阶段。尽管已有几项研究试图将混合物建模应用于 OMICS 分析,以了解胁迫物的低剂量相互作用,但目前仍不清楚分子水平上的相互作用是如何发生的,以及如何更好地利用此类方法的结果来为未来的研究和多种胁迫物的累积危害评估提供信息。因此,本研究旨在提出一种使用全局基因表达数据进行综合效应评估的概念方法,并用评估γ辐射和贫铀(DU)对大西洋鲑(Salmo salar)联合效应的案例研究来说明该方法。通过对之前发表的微阵列基因表达数据集进行重新分析,实施独立作用(IA)模型来描述综合效应的基因表达模式,并确定与理解这些胁迫物交互作用相关的关键基因集和途径。通过使用这种方法,发现 3120 个差异表达基因(DEGs)表现出相加效应,而 279 个(273 个协同作用,6 个拮抗作用)偏离了相加效应。功能分析进一步表明,多个毒性途径,如氧化应激反应、细胞周期调控、脂质代谢和免疫反应,被协同表达的 DEGs 所富集。一个关键的毒性途径——导致肿瘤发生信号增强的 DNA 损伤,被作为一个例子进行了详细的讨论,说明了如何利用这种方法。此外,还提出了一个描述综合效应建模、OMICS 分析和生物信息学整合的概念性工作流程。本研究提出了一种利用 OMICS 数据进行综合效应评估的概念框架,可为处理多种胁迫物的分子反应数据分析和解释提供新策略。