Abstract

Targeted methods that dominated toxicological research until recently did not allow for screening of all molecular changes involved in toxic response. Therefore, it is difficult to infer if all major mechanisms of toxicity have already been discovered, or if some of them are still overlooked. We used data on 591,084 unique chemical-gene interactions to identify genes and molecular pathways most sensitive to chemical exposures. The list of identified pathways did not change significantly when analyses were done on different subsets of data with non-overlapping lists of chemical compounds indicative that our dataset is saturated enough to provide unbiased results. One of the most important findings of this study is that almost every known molecular mechanism may be affected by chemical exposures. Predictably, xenobiotic metabolism pathways, and mechanisms of cellular response to stress and damage were among the most sensitive. Additionally, we identified highly sensitive molecular pathways, which are not widely recognized as major targets of toxicants, including lipid metabolism pathways, longevity regulation cascade, and cytokine-mediated signaling. These mechanisms are relevant to significant public health problems, such as aging, cancer, metabolic and autoimmune disease. Thus, public health field will benefit from future focus of toxicological research on identified sensitive mechanisms.

Highlights

  • The total burden of disease costs associated with exposures to environmental chemicals likely exceeds 10% of the global domestic product (Grandjean and Bellanger 2017)

  • Database characteristics The database used in this study (Supplementary Data File S1) consists of 641,516 individual chemical-gene interactions reported in 2,180 original studies using high-throughput gene expression analysis only

  • This database was further split into 2 subsets defined by a purposeful design of chemicals to interact with essential molecular pathways

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Summary

Introduction

The total burden of disease costs associated with exposures to environmental chemicals likely exceeds 10% of the global domestic product (Grandjean and Bellanger 2017). The number of new chemicals is rising rapidly, with the Chemical Abstract Service Registry growing from 20 million to 156 million chemicals between 2002 and 2019 (Escher et al 2020). This situation poses a significant challenge for regulatory toxicology and requires the development of new, rapid, costefficient, and reliable methods of toxicity testing. One important component of this transformation consists in a transition from outdated animal-based tests to in-vitro tests, targeting sensitive molecular mechanisms – toxicity pathways or adverse outcome pathways (AOP) (Ankley et al 2010; Haynes 2010; NRC 2007; OECD 2017; Vinken 2013). It is difficult to infer if all major mechanisms of toxicity have already been discovered, or if some of them are still overlooked

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