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Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study

CYP enzyme induction is a sensitive biomarker for phenotypic metabolic competence of in vitro test systems; it is a key event associated with thyroid disruption, and a biomarker for toxicologically relevant nuclear receptor-mediated pathways. This paper summarises the results of a multi-laboratory v...

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Autores principales: Bernasconi, Camilla, Pelkonen, Olavi, Andersson, Tommy B., Strickland, Judy, Wilk-Zasadna, Iwona, Asturiol, David, Cole, Thomas, Liska, Roman, Worth, Andrew, Müller-Vieira, Ursula, Richert, Lysiane, Chesne, Christophe, Coecke, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718736/
https://www.ncbi.nlm.nih.gov/pubmed/31158489
http://dx.doi.org/10.1016/j.tiv.2019.05.019
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author Bernasconi, Camilla
Pelkonen, Olavi
Andersson, Tommy B.
Strickland, Judy
Wilk-Zasadna, Iwona
Asturiol, David
Cole, Thomas
Liska, Roman
Worth, Andrew
Müller-Vieira, Ursula
Richert, Lysiane
Chesne, Christophe
Coecke, Sandra
author_facet Bernasconi, Camilla
Pelkonen, Olavi
Andersson, Tommy B.
Strickland, Judy
Wilk-Zasadna, Iwona
Asturiol, David
Cole, Thomas
Liska, Roman
Worth, Andrew
Müller-Vieira, Ursula
Richert, Lysiane
Chesne, Christophe
Coecke, Sandra
author_sort Bernasconi, Camilla
collection PubMed
description CYP enzyme induction is a sensitive biomarker for phenotypic metabolic competence of in vitro test systems; it is a key event associated with thyroid disruption, and a biomarker for toxicologically relevant nuclear receptor-mediated pathways. This paper summarises the results of a multi-laboratory validation study of two in vitro methods that assess the potential of chemicals to induce cytochrome P450 (CYP) enzyme activity, in particular CYP1A2, CYP2B6, and CYP3A4. The methods are based on the use of cryopreserved primary human hepatocytes (PHH) and human HepaRG cells. The validation study was coordinated by the European Union Reference Laboratory for Alternatives to Animal Testing of the European Commission's Joint Research Centre and involved a ring trial among six laboratories. The reproducibility was assessed within and between laboratories using a validation set of 13 selected chemicals (known human inducers and non-inducers) tested under blind conditions. The ability of the two methods to predict human CYP induction potential was assessed. Chemical space analysis confirmed that the selected chemicals are broadly representative of a diverse range of chemicals. The two methods were found to be reliable and relevant in vitro tools for the assessment of human CYP induction, with the HepaRG method being better suited for routine testing. Recommendations for the practical application of the two methods are proposed.
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spelling pubmed-67187362019-10-01 Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study Bernasconi, Camilla Pelkonen, Olavi Andersson, Tommy B. Strickland, Judy Wilk-Zasadna, Iwona Asturiol, David Cole, Thomas Liska, Roman Worth, Andrew Müller-Vieira, Ursula Richert, Lysiane Chesne, Christophe Coecke, Sandra Toxicol In Vitro Article CYP enzyme induction is a sensitive biomarker for phenotypic metabolic competence of in vitro test systems; it is a key event associated with thyroid disruption, and a biomarker for toxicologically relevant nuclear receptor-mediated pathways. This paper summarises the results of a multi-laboratory validation study of two in vitro methods that assess the potential of chemicals to induce cytochrome P450 (CYP) enzyme activity, in particular CYP1A2, CYP2B6, and CYP3A4. The methods are based on the use of cryopreserved primary human hepatocytes (PHH) and human HepaRG cells. The validation study was coordinated by the European Union Reference Laboratory for Alternatives to Animal Testing of the European Commission's Joint Research Centre and involved a ring trial among six laboratories. The reproducibility was assessed within and between laboratories using a validation set of 13 selected chemicals (known human inducers and non-inducers) tested under blind conditions. The ability of the two methods to predict human CYP induction potential was assessed. Chemical space analysis confirmed that the selected chemicals are broadly representative of a diverse range of chemicals. The two methods were found to be reliable and relevant in vitro tools for the assessment of human CYP induction, with the HepaRG method being better suited for routine testing. Recommendations for the practical application of the two methods are proposed. Pergamon Press 2019-10 /pmc/articles/PMC6718736/ /pubmed/31158489 http://dx.doi.org/10.1016/j.tiv.2019.05.019 Text en © 2019 European Commission http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bernasconi, Camilla
Pelkonen, Olavi
Andersson, Tommy B.
Strickland, Judy
Wilk-Zasadna, Iwona
Asturiol, David
Cole, Thomas
Liska, Roman
Worth, Andrew
Müller-Vieira, Ursula
Richert, Lysiane
Chesne, Christophe
Coecke, Sandra
Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title_full Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title_fullStr Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title_full_unstemmed Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title_short Validation of in vitro methods for human cytochrome P450 enzyme induction: Outcome of a multi-laboratory study
title_sort validation of in vitro methods for human cytochrome p450 enzyme induction: outcome of a multi-laboratory study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718736/
https://www.ncbi.nlm.nih.gov/pubmed/31158489
http://dx.doi.org/10.1016/j.tiv.2019.05.019
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