基于组学的污染物高通量毒理学筛查与风险评估

Translated title of the contribution: Omics-based high throughput toxicity screening and risk assessment of pollutants

Lu Yan, Xiao Gou, Pu Xia, Ruize Gao, Huimin Ji, Wei Shi, Hongxia Yu, Xiaowei Zhang*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Screening priority pollutants with high toxicity and risk potential from a large number of environmental chemical pollutants is the prerequisite for prevention and control of environmental risks. After entering the living system, toxic pollutants can induce adverse outcomes through a series of disturbed molecular targets and biological pathways. Existing high-throughput toxicity screening methods rely on few and isolated cellular or molecular endpoints, making it difficult to capture the key biological processes that cause toxicity and to determine the direct relationship between chemical pollutants and disease. Meanwhile, the awareness is increasing that we are exposed to a true cocktail of chemicals, among which only a fraction has been identified through analytical methods. Integrated bioanalytical approaches, such as effect-directed analysis and toxicity identification evaluation (TIE), have been used to identify risk drivers in complex mixture pollutants. However, it is still difficult to elucidate the molecular toxicological drivers of chemical stress in the environment.

Toxicogenomics take advantage of genome-wide coverage, high throughput, and big data capacity that are associated with omics technologies to achieve technology innovation in screening and risk assessment of chemical pollutants. We reviewed the technical advantages and the recent progress of toxicogenomic methodology in high-throughput toxicological screening and risk assessment of chemical pollutants from four aspects with specific research cases. To identify the molecular events initiated by toxic pollutants, toxicogenomics could uncover a large number of molecular events and pathways potentially disturbed at the early development stage of toxicity. Dose-dependent transcriptomes for high-throughput chemical testing have been developed to quantitatively assess responses induced by chemical pollutants at the molecular level, which improve the sensitivity of identifying bioactivity by 1–3 orders of magnitude. To uncover the biological pathways of adverse health outcome by chemical pollutants, systemic toxicological assessment by omics strategies provide mechanistic information for chemical pollution screening and health risk assessment at multiple biological levels. Through biological pathway enrichment analysis, such as the gene ontology (GO) and kyoto encyclopedia of genes and genomes (KEGG) pathway, the molecular mechanistic information of toxicity could be captured. Moreover, multi-omics integration allows for multi-scale, comprehensive biological network analysis, which provide a systematic understanding of toxicity pathways or adverse outcome pathways (AOPs) to guide ecological and human health risk assessments.

For human diseases diagnostics, functional genomics provide a new tool to explore mechanisms of individual disease risk and susceptibility under toxic pollutants exposure. Variations of individual susceptibility to toxicant-induced disease are largely due to genetic susceptibility across different populations. The direct relationship among pollutants, genes and adverse outcomes could be established by combining functional genomics and molecular epidemiological approaches.

Finally, for risk management of complex mixture pollutants, it is important to assess the overall toxicity effects of the pool of pollutants and identify the key toxic pollutant. The combination of high-throughput bioassays and chemical analysis can be used to identify the highly bioactive fraction and to screen the key chemical pollutant that pose ecological and health risks. Recently, progresses have been made in integrating transcriptomic techniques with molecular toxicity identification and evaluation (mTIE) to assess the overall effects of mixtures and distinguish the key pollutants in inducing the corresponding biological responses. Particularly, dose-response transcriptome could be used to quantitatively evaluate the overall toxic effects and to guide the key toxicant identification by high mechanistic resolution.

In summary, the development of omics-based high-throughput toxicity screening technologies will strongly support accurate environmental risk assessment of conventional and new pollutants in the future.

Translated title of the contributionOmics-based high throughput toxicity screening and risk assessment of pollutants
Original languageChinese
Pages (from-to)4159-4169
Number of pages11
JournalKexue Tongbao/Chinese Science Bulletin
Volume67
Issue number35
DOIs
Publication statusPublished - 13 Oct 2022

Bibliographical note

Publisher Copyright:
© 2022 Chinese Academy of Sciences. All rights reserved.

Keywords

  • biological pathways
  • chemical pollutants
  • human diseases
  • mixture pollutants
  • molecular targets
  • toxicogenomics

ASJC Scopus subject areas

  • General

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