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Demonstrating the reliability of in vivo metabolomics based chemical grouping: towards best practice.
Viant, Mark R; Amstalden, E; Athersuch, T; Bouhifd, M; Camuzeaux, S; Crizer, D M; Driemert, P; Ebbels, T; Ekman, D; Flick, B; Giri, V; Gómez-Romero, M; Haake, V; Herold, M; Kende, A; Lai, F; Leonards, P E G; Lim, P P; Lloyd, G R; Mosley, J; Namini, C; Rice, J R; Romano, S; Sands, C; Smith, M J; Sobanski, T; Southam, A D; Swindale, L; van Ravenzwaay, B; Walk, T; Weber, R J M; Zickgraf, F M; Kamp, H.
Afiliação
  • Viant MR; Phenome Centre Birmingham, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK. m.viant@bham.ac.uk.
  • Amstalden E; Amsterdam Institute for Life and Environment (A-LIFE), Vrije Universiteit Amsterdam, De Boelelaan 1085, 1081 HV, Amsterdam, The Netherlands.
  • Athersuch T; Division of Systems Medicine, Department of Metabolism, Digestion and Reproduction, Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.
  • Bouhifd M; European Chemicals Agency, Telakkakatu 6, FI-00121, Helsinki, Finland.
  • Camuzeaux S; Department of Metabolism, Digestion and Reproduction, National Phenome Centre, Imperial College London, London, W12 0NN, UK.
  • Crizer DM; Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
  • Driemert P; BASF Metabolome Solutions GmbH, Tegeler Weg 33, 10589, Berlin, Germany.
  • Ebbels T; Division of Systems Medicine, Department of Metabolism, Digestion and Reproduction, Imperial College London, Hammersmith Hospital, Du Cane Road, London, W12 0NN, UK.
  • Ekman D; Center for Environmental Measurement and Modeling, Environmental Protection Agency, Athens, GA, 30605, USA.
  • Flick B; BASF SE, Carl-Bosch-Str 38, 67056, Ludwigshafen, Germany.
  • Giri V; NUVISAN ICB GmbH, Toxicology, 13353, Berlin, Germany.
  • Gómez-Romero M; BASF SE, Carl-Bosch-Str 38, 67056, Ludwigshafen, Germany.
  • Haake V; Department of Metabolism, Digestion and Reproduction, National Phenome Centre, Imperial College London, London, W12 0NN, UK.
  • Herold M; BASF Metabolome Solutions GmbH, Tegeler Weg 33, 10589, Berlin, Germany.
  • Kende A; BASF Metabolome Solutions GmbH, Tegeler Weg 33, 10589, Berlin, Germany.
  • Lai F; Syngenta, Jealott's Hill International Research Centre, Bracknell, RG42 6EY, UK.
  • Leonards PEG; Syngenta, Jealott's Hill International Research Centre, Bracknell, RG42 6EY, UK.
  • Lim PP; Amsterdam Institute for Life and Environment (A-LIFE), Vrije Universiteit Amsterdam, De Boelelaan 1085, 1081 HV, Amsterdam, The Netherlands.
  • Lloyd GR; Syngenta, Jealott's Hill International Research Centre, Bracknell, RG42 6EY, UK.
  • Mosley J; Phenome Centre Birmingham, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Namini C; Center for Environmental Measurement and Modeling, Environmental Protection Agency, Athens, GA, 30605, USA.
  • Rice JR; Center for Environmental Measurement and Modeling, Environmental Protection Agency, Athens, GA, 30605, USA.
  • Romano S; Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
  • Sands C; Center for Environmental Measurement and Modeling, Environmental Protection Agency, Athens, GA, 30605, USA.
  • Smith MJ; Department of Metabolism, Digestion and Reproduction, National Phenome Centre, Imperial College London, London, W12 0NN, UK.
  • Sobanski T; Phenome Centre Birmingham, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Southam AD; European Chemicals Agency, Telakkakatu 6, FI-00121, Helsinki, Finland.
  • Swindale L; Phenome Centre Birmingham, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • van Ravenzwaay B; Syngenta, Jealott's Hill International Research Centre, Bracknell, RG42 6EY, UK.
  • Walk T; BASF SE, Carl-Bosch-Str 38, 67056, Ludwigshafen, Germany.
  • Weber RJM; Environmental Sciences Consulting, 67122, Altrip, Germany.
  • Zickgraf FM; BASF Metabolome Solutions GmbH, Tegeler Weg 33, 10589, Berlin, Germany.
  • Kamp H; Phenome Centre Birmingham, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Arch Toxicol ; 98(4): 1111-1123, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38368582
ABSTRACT
While grouping/read-across is widely used to fill data gaps, chemical registration dossiers are often rejected due to weak category justifications based on structural similarity only. Metabolomics provides a route to robust chemical categories via evidence of shared molecular effects across source and target substances. To gain international acceptance, this approach must demonstrate high reliability, and best-practice guidance is required. The MetAbolomics ring Trial for CHemical groupING (MATCHING), comprising six industrial, government and academic ring-trial partners, evaluated inter-laboratory reproducibility and worked towards best-practice. An independent team selected eight substances (WY-14643, 4-chloro-3-nitroaniline, 17α-methyl-testosterone, trenbolone, aniline, dichlorprop-p, 2-chloroaniline, fenofibrate); ring-trial partners were blinded to their identities and modes-of-action. Plasma samples were derived from 28-day rat tests (two doses per substance), aliquoted, and distributed to partners. Each partner applied their preferred liquid chromatography-mass spectrometry (LC-MS) metabolomics workflows to acquire, process, quality assess, statistically analyze and report their grouping results to the European Chemicals Agency, to ensure the blinding conditions of the ring trial. Five of six partners, whose metabolomics datasets passed quality control, correctly identified the grouping of eight test substances into three categories, for both male and female rats. Strikingly, this was achieved even though a range of metabolomics approaches were used. Through assessing intrastudy quality-control samples, the sixth partner observed high technical variation and was unable to group the substances. By comparing workflows, we conclude that some heterogeneity in metabolomics methods is not detrimental to consistent grouping, and that assessing data quality prior to grouping is essential. We recommend development of international guidance for quality-control acceptance criteria. This study demonstrates the reliability of metabolomics for chemical grouping and works towards best-practice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metabolômica / Espectrometria de Massa com Cromatografia Líquida Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metabolômica / Espectrometria de Massa com Cromatografia Líquida Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article