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G × E interactions as a basis for toxicological uncertainty.
Suciu, Ilinca; Pamies, David; Peruzzo, Roberta; Wirtz, Petra H; Smirnova, Lena; Pallocca, Giorgia; Hauck, Christof; Cronin, Mark T D; Hengstler, Jan G; Brunner, Thomas; Hartung, Thomas; Amelio, Ivano; Leist, Marcel.
Afiliação
  • Suciu I; In Vitro Toxicology and Biomedicine, Department Inaugurated By the Doerenkamp-Zbinden Foundation, University of Konstanz, Universitaetsstr. 10, 78457, Constance, Germany.
  • Pamies D; Department of Biological Sciences, University of Lausanne, 1005, Lausanne, Switzerland.
  • Peruzzo R; Department of Molecular and Cell Biology, University of California, Berkeley, CA, 94720, USA.
  • Wirtz PH; Centre for the Advanced Study of Collective Behaviour, University of Konstanz, 78457, Constance, Germany.
  • Smirnova L; Biological Work and Health Psychology, Department of Psychology, University of Konstanz, 78457, Constance, Germany.
  • Pallocca G; Center for Alternatives to Animal Testing (CAAT), Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD, 21205, USA.
  • Hauck C; CAAT Europe, University of Konstanz, 78457, Constance, Germany.
  • Cronin MTD; Department of Cell Biology, University of Konstanz, 78457, Constance, Germany.
  • Hengstler JG; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool, L3 3AF, UK.
  • Brunner T; Leibniz Research Centre for Working Environment and Human Factors, Technical University Dortmund, 44139, Dortmund, Germany.
  • Hartung T; Biochemical Pharmacology, Department of Biology, University of Konstanz, 78457, Constance, Germany.
  • Amelio I; Center for Alternatives to Animal Testing (CAAT), Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD, 21205, USA.
  • Leist M; CAAT Europe, University of Konstanz, 78457, Constance, Germany.
Arch Toxicol ; 97(7): 2035-2049, 2023 07.
Article em En | MEDLINE | ID: mdl-37258688
ABSTRACT
To transfer toxicological findings from model systems, e.g. animals, to humans, standardized safety factors are applied to account for intra-species and inter-species variabilities. An alternative approach would be to measure and model the actual compound-specific uncertainties. This biological concept assumes that all observed toxicities depend not only on the exposure situation (environment = E), but also on the genetic (G) background of the model (G × E). As a quantitative discipline, toxicology needs to move beyond merely qualitative G × E concepts. Research programs are required that determine the major biological variabilities affecting toxicity and categorize their relative weights and contributions. In a complementary approach, detailed case studies need to explore the role of genetic backgrounds in the adverse effects of defined chemicals. In addition, current understanding of the selection and propagation of adverse outcome pathways (AOP) in different biological environments is very limited. To improve understanding, a particular focus is required on modulatory and counter-regulatory steps. For quantitative approaches to address uncertainties, the concept of "genetic" influence needs a more precise definition. What is usually meant by this term in the context of G × E are the protein functions encoded by the genes. Besides the gene sequence, the regulation of the gene expression and function should also be accounted for. The widened concept of past and present "gene expression" influences is summarized here as Ge. Also, the concept of "environment" needs some re-consideration in situations where exposure timing (Et) is pivotal prolonged or repeated exposure to the insult (chemical, physical, life style) affects Ge. This implies that it changes the model system. The interaction of Ge with Et might be denoted as Ge × Et. We provide here general explanations and specific examples for this concept and show how it could be applied in the context of New Approach Methodologies (NAM).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rotas de Resultados Adversos Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rotas de Resultados Adversos Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article