Evaluating the performance of multi-omics integration: a thyroid toxicity case study

Multi-omics data integration has been repeatedly discussed as the way forward to more comprehensively cover the molecular responses of cells or organisms to chemical exposure in systems toxicology and regulatory risk assessment. In Canzler et al. (Arch Toxicol 94(2):371-388. https://doi.org/10.1007/s00204-020-02656-y ), we reviewed the state of the art in applying multi-omics approaches in toxicological research and chemical risk assessment. We developed best practices for the experimental design of multi-omics studies, omics data acquisition, and subsequent omics data integration. We found that multi-omics data sets for toxicological research questions were generally rare, with no data sets comprising more than two omics layers adhering to these best practices. Due to these limitations, we could not fully assess the benefits of different data integration approaches or quantitatively evaluate the contribution of various omics layers for toxicological research questions. Here, we report on a multi-omics study on thyroid toxicity that we conducted in compliance with these best practices. We induced direct and indirect thyroid toxicity through Propylthiouracil (PTU) and Phenytoin, respectively, in a 28-day plus 14-day recovery oral rat toxicity study. We collected clinical and histopathological data and six omics layers, including the long and short transcriptome, proteome, phosphoproteome, and metabolome from plasma, thyroid, and liver. We demonstrate that the multi-omics approach is superior to single-omics in detecting responses at the regulatory pathway level. We also show how combining omics data with clinical and histopathological parameters facilitates the interpretation of the data. Furthermore, we illustrate how multi-omics integration can hint at the involvement of non-coding RNAs in post-transcriptional regulation. Also, we show that multi-omics facilitates grouping, and we assess how much information individual and combinations of omics layers contribute to this approach.

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Publication Details

Journal
Archives of Toxicology
Published
2024-10-23
DOI
https://doi.org/10.1007/s00204-024-03876-2
Citations
5
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
1.17

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article

Evaluating the performance of multi-omics integration: a thyroid toxicity case study

Hervé Seitz, Roland Buesen, Sebastian Canzler, Sophie Mockly et al.
5 citations
Archives of Toxicology
Bioinformatics and Genomic Networks
1.17
article

Evaluating the performance of multi-omics integration: a thyroid toxicity case study

Hervé Seitz, Roland Buesen, Sebastian Canzler, Sophie Mockly, Ulrike Elisabeth Rolle-Kampczyk, Kristin Schubert, Volker Haake, Hennicke Kamp, Maike Huisinga, S Schreiber, Jörg Hackermüller, Zhipeng Wang, Martin von Bergen
article en
5 citations

Abstract

Multi-omics data integration has been repeatedly discussed as the way forward to more comprehensively cover the molecular responses of cells or organisms to chemical exposure in systems toxicology and regulatory risk assessment. In Canzler et al. (Arch Toxicol 94(2):371-388. https://doi.org/10.1007/s00204-020-02656-y ), we reviewed the state of the art in applying multi-omics approaches in toxicological research and chemical risk assessment. We developed best practices for the experimental design of multi-omics studies, omics data acquisition, and subsequent omics data integration. We found that multi-omics data sets for toxicological research questions were generally rare, with no data sets comprising more than two omics layers adhering to these best practices. Due to these limitations, we could not fully assess the benefits of different data integration approaches or quantitatively evaluate the contribution of various omics layers for toxicological research questions. Here, we report on a multi-omics study on thyroid toxicity that we conducted in compliance with these best practices. We induced direct and indirect thyroid toxicity through Propylthiouracil (PTU) and Phenytoin, respectively, in a 28-day plus 14-day recovery oral rat toxicity study. We collected clinical and histopathological data and six omics layers, including the long and short transcriptome, proteome, phosphoproteome, and metabolome from plasma, thyroid, and liver. We demonstrate that the multi-omics approach is superior to single-omics in detecting responses at the regulatory pathway level. We also show how combining omics data with clinical and histopathological parameters facilitates the interpretation of the data. Furthermore, we illustrate how multi-omics integration can hint at the involvement of non-coding RNAs in post-transcriptional regulation. Also, we show that multi-omics facilitates grouping, and we assess how much information individual and combinations of omics layers contribute to this approach.

Archives of ToxicologyVol. 99(1)
Centre National de la Recherche Scientifique (FR), Helmholtz Centre for Environmental Research (DE), Université de Montpellier (FR), BASF (Germany) (DE), Biobyte Solutions (Germany) (DE), Institut de Génétique Humaine (FR)
European Chemical Industry Council, European Commission, HORIZON EUROPE Framework Programme
Good health and well-being
Openalex Percentile: Top 21%
Bioinformatics and Genomic Networks
1.17
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