Helmholtz Centre for Environmental Research - UFZ, 04318, Leipzig, Germany.
Institut de Génétique Humaine UMR 9002 CNRS-Université de Montpellier, 34396, Montpellier Cedex 5, France.
Arch Toxicol. 2020 Feb;94(2):371-388. doi: 10.1007/s00204-020-02656-y. Epub 2020 Feb 8.
Exposure of cells or organisms to chemicals can trigger a series of effects at the regulatory pathway level, which involve changes of levels, interactions, and feedback loops of biomolecules of different types. A single-omics technique, e.g., transcriptomics, will detect biomolecules of one type and thus can only capture changes in a small subset of the biological cascade. Therefore, although applying single-omics analyses can lead to the identification of biomarkers for certain exposures, they cannot provide a systemic understanding of toxicity pathways or adverse outcome pathways. Integration of multiple omics data sets promises a substantial improvement in detecting this pathway response to a toxicant, by an increase of information as such and especially by a systemic understanding. Here, we report the findings of a thorough evaluation of the prospects and challenges of multi-omics data integration in toxicological research. We review the availability of such data, discuss options for experimental design, evaluate methods for integration and analysis of multi-omics data, discuss best practices, and identify knowledge gaps. Re-analyzing published data, we demonstrate that multi-omics data integration can considerably improve the confidence in detecting a pathway response. Finally, we argue that more data need to be generated from studies with a multi-omics-focused design, to define which omics layers contribute most to the identification of a pathway response to a toxicant.
细胞或生物体暴露于化学物质会在调控通路层面引发一系列效应,其中涉及不同类型生物分子的水平变化、相互作用和反馈环。单一组学技术,如转录组学,只能检测到一种类型的生物分子,因此只能捕捉到生物级联反应中的一小部分变化。因此,尽管应用单一组学分析可以识别某些暴露的生物标志物,但它们不能提供对毒性通路或不良结局通路的系统理解。整合多个组学数据集有望通过增加信息量,特别是通过系统理解,极大地提高对毒物的通路反应的检测能力。在这里,我们报告了对毒理学研究中多组学数据整合的前景和挑战进行全面评估的结果。我们回顾了这些数据的可用性,讨论了实验设计的选择,评估了整合和分析多组学数据的方法,讨论了最佳实践,并确定了知识空白。我们重新分析了已发表的数据,证明了多组学数据的整合可以大大提高检测通路反应的置信度。最后,我们认为需要从具有多组学重点设计的研究中生成更多的数据,以确定哪些组学层对识别毒物的通路反应最有贡献。