TY - JOUR
T1 - Advancing chemical safety assessment through an omics-based characterization of the test system-chemical interaction
AU - del Giudice, Giusy
AU - Migliaccio, Giorgia
AU - D’Alessandro, Nicoletta
AU - Saarimäki, Laura Aliisa
AU - Torres Maia, Marcella
AU - Annala, Maria Emilia
AU - Leppänen, Jenni
AU - Möbus, Lena
AU - Pavel, Alisa
AU - Vaani, Maaret
AU - Vallius, Anna
AU - Ylä-Outinen, Laura
AU - Greco, Dario
AU - Serra, Angela
N1 - Publisher Copyright:
Copyright © 2023 del Giudice, Migliaccio, D’Alessandro, Saarimäki, Torres Maia, Annala, Leppänen, Mӧbus, Pavel, Vaani, Vallius, Ylä‐Outinen, Greco and Serra.
PY - 2023
Y1 - 2023
N2 - Assessing chemical safety is essential to evaluate the potential risks of chemical exposure to human health and the environment. Traditional methods relying on animal testing are being replaced by 3R (reduction, refinement, and replacement) principle-based alternatives, mainly depending on in vitro test methods and the Adverse Outcome Pathway framework. However, these approaches often focus on the properties of the compound, missing the broader chemical-biological interaction perspective. Currently, the lack of comprehensive molecular characterization of the in vitro test system results in limited real-world representation and contextualization of the toxicological effect under study. Leveraging omics data strengthens the understanding of the responses of different biological systems, emphasizing holistic chemical-biological interactions when developing in vitro methods. Here, we discuss the relevance of meticulous test system characterization on two safety assessment relevant scenarios and how omics-based, data-driven approaches can improve the future generation of alternative methods.
AB - Assessing chemical safety is essential to evaluate the potential risks of chemical exposure to human health and the environment. Traditional methods relying on animal testing are being replaced by 3R (reduction, refinement, and replacement) principle-based alternatives, mainly depending on in vitro test methods and the Adverse Outcome Pathway framework. However, these approaches often focus on the properties of the compound, missing the broader chemical-biological interaction perspective. Currently, the lack of comprehensive molecular characterization of the in vitro test system results in limited real-world representation and contextualization of the toxicological effect under study. Leveraging omics data strengthens the understanding of the responses of different biological systems, emphasizing holistic chemical-biological interactions when developing in vitro methods. Here, we discuss the relevance of meticulous test system characterization on two safety assessment relevant scenarios and how omics-based, data-driven approaches can improve the future generation of alternative methods.
KW - AOP
KW - chemical safety assessment
KW - chemical-biological interaction
KW - mechanism of action
KW - nanosafety
KW - new approach methodologies
KW - test system characterization
KW - toxicogenomics
U2 - 10.3389/ftox.2023.1294780
DO - 10.3389/ftox.2023.1294780
M3 - Article
AN - SCOPUS:85177688278
SN - 2673-3080
VL - 5
JO - Frontiers in Toxicology
JF - Frontiers in Toxicology
M1 - 1294780
ER -