The use of systems biology in chemical risk assessment

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The use of systems biology in chemical risk assessment. / Aguayo-Orozco, Alejandro; Taboureau, Olivier; Brunak, Søren.

In: Current Opinion in Toxicology, Vol. 15, 2019, p. 48-54.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Aguayo-Orozco, A, Taboureau, O & Brunak, S 2019, 'The use of systems biology in chemical risk assessment', Current Opinion in Toxicology, vol. 15, pp. 48-54. https://doi.org/10.1016/j.cotox.2019.03.003

APA

Aguayo-Orozco, A., Taboureau, O., & Brunak, S. (2019). The use of systems biology in chemical risk assessment. Current Opinion in Toxicology, 15, 48-54. https://doi.org/10.1016/j.cotox.2019.03.003

Vancouver

Aguayo-Orozco A, Taboureau O, Brunak S. The use of systems biology in chemical risk assessment. Current Opinion in Toxicology. 2019;15:48-54. https://doi.org/10.1016/j.cotox.2019.03.003

Author

Aguayo-Orozco, Alejandro ; Taboureau, Olivier ; Brunak, Søren. / The use of systems biology in chemical risk assessment. In: Current Opinion in Toxicology. 2019 ; Vol. 15. pp. 48-54.

Bibtex

@article{9409b53faf0d4bd9ab0bfe9a800a42a9,
title = "The use of systems biology in chemical risk assessment",
abstract = "Risk assessment of toxicological compounds has traditionally relied upon animal experimentation. Omics technologies, especially genomics and proteomics, generate large amounts of data on genome-wide gene expression profiles, protein expression, and protein interaction with xenobiotics (notably toxic ones), enabling the study of chemical action across multiple scales of complexity from molecular to systems levels. This allows detailed exploration of the mechanisms of toxicity. Although all omics technologies may contribute to better understanding of the toxicological impact of chemicals, their application in chemical risk assessment has not yet been recommended for regulatory purposes. With the recent development of the adverse outcome pathway concept, the combination of the modular framework of adverse outcome pathway, together with the network organisation within systems biology, offers an opportunity to shift the paradigm of chemical risk assessment towards a better understanding of chemical toxicology mechanisms. In this review, we discuss the advantages of the use of systems biology tools in chemical risk assessment, as well as the challenges they present, such as model over-parametrisation in quantitative modelling, data gap management in poorly studied substances and the lack of expertise in bridging the new approaches to regulatory levels.",
keywords = "Adverse outcome pathway, Chemical risk assessment, Integrated approaches to testing and assessment, Read across, Systems biology, Systems toxicology",
author = "Alejandro Aguayo-Orozco and Olivier Taboureau and S{\o}ren Brunak",
year = "2019",
doi = "10.1016/j.cotox.2019.03.003",
language = "English",
volume = "15",
pages = "48--54",
journal = "Current Opinion in Toxicology",
issn = "2468-2020",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - The use of systems biology in chemical risk assessment

AU - Aguayo-Orozco, Alejandro

AU - Taboureau, Olivier

AU - Brunak, Søren

PY - 2019

Y1 - 2019

N2 - Risk assessment of toxicological compounds has traditionally relied upon animal experimentation. Omics technologies, especially genomics and proteomics, generate large amounts of data on genome-wide gene expression profiles, protein expression, and protein interaction with xenobiotics (notably toxic ones), enabling the study of chemical action across multiple scales of complexity from molecular to systems levels. This allows detailed exploration of the mechanisms of toxicity. Although all omics technologies may contribute to better understanding of the toxicological impact of chemicals, their application in chemical risk assessment has not yet been recommended for regulatory purposes. With the recent development of the adverse outcome pathway concept, the combination of the modular framework of adverse outcome pathway, together with the network organisation within systems biology, offers an opportunity to shift the paradigm of chemical risk assessment towards a better understanding of chemical toxicology mechanisms. In this review, we discuss the advantages of the use of systems biology tools in chemical risk assessment, as well as the challenges they present, such as model over-parametrisation in quantitative modelling, data gap management in poorly studied substances and the lack of expertise in bridging the new approaches to regulatory levels.

AB - Risk assessment of toxicological compounds has traditionally relied upon animal experimentation. Omics technologies, especially genomics and proteomics, generate large amounts of data on genome-wide gene expression profiles, protein expression, and protein interaction with xenobiotics (notably toxic ones), enabling the study of chemical action across multiple scales of complexity from molecular to systems levels. This allows detailed exploration of the mechanisms of toxicity. Although all omics technologies may contribute to better understanding of the toxicological impact of chemicals, their application in chemical risk assessment has not yet been recommended for regulatory purposes. With the recent development of the adverse outcome pathway concept, the combination of the modular framework of adverse outcome pathway, together with the network organisation within systems biology, offers an opportunity to shift the paradigm of chemical risk assessment towards a better understanding of chemical toxicology mechanisms. In this review, we discuss the advantages of the use of systems biology tools in chemical risk assessment, as well as the challenges they present, such as model over-parametrisation in quantitative modelling, data gap management in poorly studied substances and the lack of expertise in bridging the new approaches to regulatory levels.

KW - Adverse outcome pathway

KW - Chemical risk assessment

KW - Integrated approaches to testing and assessment

KW - Read across

KW - Systems biology

KW - Systems toxicology

U2 - 10.1016/j.cotox.2019.03.003

DO - 10.1016/j.cotox.2019.03.003

M3 - Review

AN - SCOPUS:85066997271

VL - 15

SP - 48

EP - 54

JO - Current Opinion in Toxicology

JF - Current Opinion in Toxicology

SN - 2468-2020

ER -

ID: 228150650