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ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters

ERGO (EndocRine Guideline Optimization) is the acronym of a European Union-funded research and innovation action, that aims to break down the wall between mammalian and non-mammalian vertebrate regulatory testing of endocrine disruptors (EDs), by identifying, developing and aligning thyroid-related...

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Autores principales: Holbech, Henrik, Matthiessen, Peter, Hansen, Martin, Schüürmann, Gerrit, Knapen, Dries, Reuver, Marieke, Flamant, Frédéric, Sachs, Laurent, Kloas, Werner, Hilscherova, Klara, Leonard, Marc, Arning, Jürgen, Strauss, Volker, Iguchi, Taisen, Baumann, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215679/
https://www.ncbi.nlm.nih.gov/pubmed/32331419
http://dx.doi.org/10.3390/ijms21082954
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author Holbech, Henrik
Matthiessen, Peter
Hansen, Martin
Schüürmann, Gerrit
Knapen, Dries
Reuver, Marieke
Flamant, Frédéric
Sachs, Laurent
Kloas, Werner
Hilscherova, Klara
Leonard, Marc
Arning, Jürgen
Strauss, Volker
Iguchi, Taisen
Baumann, Lisa
author_facet Holbech, Henrik
Matthiessen, Peter
Hansen, Martin
Schüürmann, Gerrit
Knapen, Dries
Reuver, Marieke
Flamant, Frédéric
Sachs, Laurent
Kloas, Werner
Hilscherova, Klara
Leonard, Marc
Arning, Jürgen
Strauss, Volker
Iguchi, Taisen
Baumann, Lisa
author_sort Holbech, Henrik
collection PubMed
description ERGO (EndocRine Guideline Optimization) is the acronym of a European Union-funded research and innovation action, that aims to break down the wall between mammalian and non-mammalian vertebrate regulatory testing of endocrine disruptors (EDs), by identifying, developing and aligning thyroid-related biomarkers and endpoints (B/E) for the linkage of effects between vertebrate classes. To achieve this, an adverse outcome pathway (AOP) network covering various modes of thyroid hormone disruption (THD) in multiple vertebrate classes will be developed. The AOP development will be based on existing and new data from in vitro and in vivo experiments with fish, amphibians and mammals, using a battery of different THDs. This will provide the scientifically plausible and evidence-based foundation for the selection of B/E and assays in lower vertebrates, predictive of human health outcomes. These assays will be prioritized for validation at OECD (Organization for Economic Cooperation and Development) level. ERGO will re-think ED testing strategies from in silico methods to in vivo testing and develop, optimize and validate existing in vivo and early life-stage OECD guidelines, as well as new in vitro protocols for THD. This strategy will reduce requirements for animal testing by preventing duplication of testing in mammals and non-mammalian vertebrates and increase the screening capacity to enable more chemicals to be tested for ED properties.
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spelling pubmed-72156792020-05-22 ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters Holbech, Henrik Matthiessen, Peter Hansen, Martin Schüürmann, Gerrit Knapen, Dries Reuver, Marieke Flamant, Frédéric Sachs, Laurent Kloas, Werner Hilscherova, Klara Leonard, Marc Arning, Jürgen Strauss, Volker Iguchi, Taisen Baumann, Lisa Int J Mol Sci Project Report ERGO (EndocRine Guideline Optimization) is the acronym of a European Union-funded research and innovation action, that aims to break down the wall between mammalian and non-mammalian vertebrate regulatory testing of endocrine disruptors (EDs), by identifying, developing and aligning thyroid-related biomarkers and endpoints (B/E) for the linkage of effects between vertebrate classes. To achieve this, an adverse outcome pathway (AOP) network covering various modes of thyroid hormone disruption (THD) in multiple vertebrate classes will be developed. The AOP development will be based on existing and new data from in vitro and in vivo experiments with fish, amphibians and mammals, using a battery of different THDs. This will provide the scientifically plausible and evidence-based foundation for the selection of B/E and assays in lower vertebrates, predictive of human health outcomes. These assays will be prioritized for validation at OECD (Organization for Economic Cooperation and Development) level. ERGO will re-think ED testing strategies from in silico methods to in vivo testing and develop, optimize and validate existing in vivo and early life-stage OECD guidelines, as well as new in vitro protocols for THD. This strategy will reduce requirements for animal testing by preventing duplication of testing in mammals and non-mammalian vertebrates and increase the screening capacity to enable more chemicals to be tested for ED properties. MDPI 2020-04-22 /pmc/articles/PMC7215679/ /pubmed/32331419 http://dx.doi.org/10.3390/ijms21082954 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Project Report
Holbech, Henrik
Matthiessen, Peter
Hansen, Martin
Schüürmann, Gerrit
Knapen, Dries
Reuver, Marieke
Flamant, Frédéric
Sachs, Laurent
Kloas, Werner
Hilscherova, Klara
Leonard, Marc
Arning, Jürgen
Strauss, Volker
Iguchi, Taisen
Baumann, Lisa
ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title_full ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title_fullStr ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title_full_unstemmed ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title_short ERGO: Breaking Down the Wall between Human Health and Environmental Testing of Endocrine Disrupters
title_sort ergo: breaking down the wall between human health and environmental testing of endocrine disrupters
topic Project Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215679/
https://www.ncbi.nlm.nih.gov/pubmed/32331419
http://dx.doi.org/10.3390/ijms21082954
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