Systems Toxicology: Real World Applications and Opportunities

Thomas Hartung, Rex E FitzGerald, Paul Jennings, Gary R Mirams, Manuel C Peitsch, Amin Rostami-Hodjegan, Imran Shah, Martin F Wilks, Shana J Sturla

Research output: Contribution to JournalReview articleAcademicpeer-review

Abstract

Systems Toxicology aims to change the basis of how adverse biological effects of xenobiotics are characterized from empirical end points to describing modes of action as adverse outcome pathways and perturbed networks. Toward this aim, Systems Toxicology entails the integration of in vitro and in vivo toxicity data with computational modeling. This evolving approach depends critically on data reliability and relevance, which in turn depends on the quality of experimental models and bioanalysis techniques used to generate toxicological data. Systems Toxicology involves the use of large-scale data streams ("big data"), such as those derived from omics measurements that require computational means for obtaining informative results. Thus, integrative analysis of multiple molecular measurements, particularly acquired by omics strategies, is a key approach in Systems Toxicology. In recent years, there have been significant advances centered on in vitro test systems and bioanalytical strategies, yet a frontier challenge concerns linking observed network perturbations to phenotypes, which will require understanding pathways and networks that give rise to adverse responses. This summary perspective from a 2016 Systems Toxicology meeting, an international conference held in the Alps of Switzerland, describes the limitations and opportunities of selected emerging applications in this rapidly advancing field. Systems Toxicology aims to change the basis of how adverse biological effects of xenobiotics are characterized, from empirical end points to pathways of toxicity. This requires the integration of in vitro and in vivo data with computational modeling. Test systems and bioanalytical technologies have made significant advances, but ensuring data reliability and relevance is an ongoing concern. The major challenge facing the new pathway approach is determining how to link observed network perturbations to phenotypic toxicity.

Original languageEnglish
Pages (from-to)870-882
Number of pages13
JournalChemical Research in Toxicology
Volume30
Issue number4
Early online date31 Mar 2017
DOIs
Publication statusPublished - 17 Apr 2017

Bibliographical note

This article is part of the Systems Toxicology II special issue.

Funding

G.R.M. gratefully acknowledges support from a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (Grant Number 101222/Z/13/Z). P.J. acknowledges support of the European Union’s seventh Framework Programme (FP7/2007-2013) under grant agreement no 202222, Predict-IV. S.J.S. acknowledges support of the Swiss National Science Foundation (Grant Number 156280), the European Research Council (Grant Number 680920), and the European Union’s Horizon 2020 Program (Grant Number 633172). R.E.F. and M.F.W. are at the Swiss Centre for Applied Human Toxicology, which is funded by the Swiss Confederation and the Universities of Basel, Geneva, and Lausanne; T.H. is funded by the NIH transformative research project on “Mapping the Human Toxome by Systems Toxicology” (R01ES020750).

FundersFunder number
Swiss Confederation and the Universities of Basel, Geneva
National Institutes of Health
National Institute of Environmental Health SciencesR01ES020750
Wellcome Trust
Seventh Framework Programme202222
Royal Society101222/Z/13/Z
European Research Council680920
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung156280
Seventh Framework Programme
Horizon 2020633172
Swiss Centre for Applied Human Toxicology

    Keywords

    • Half-Life
    • Heart
    • High-Throughput Screening Assays
    • Humans
    • Journal Article
    • Kidney
    • Liver
    • Metabolomics
    • Models, Theoretical
    • Proteomics
    • Xenobiotics

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