TY - JOUR
T1 - New approach methods to improve human health risk assessment of thyroid hormone system disruption–a PARC project
AU - Ramhøj, Louise
AU - Axelstad, Marta
AU - Baert, Yoni
AU - Cañas-Portilla, Ana I.
AU - Chalmel, Frédéric
AU - Dahmen, Lars
AU - De La Vieja, Antonio
AU - Evrard, Bertrand
AU - Haigis, Ann Cathrin
AU - Hamers, Timo
AU - Heikamp, Kim
AU - Holbech, Henrik
AU - Iglesias-Hernandez, Patricia
AU - Knapen, Dries
AU - Marchandise, Lorna
AU - Morthorst, Jane E.
AU - Nikolov, Nikolai Georgiev
AU - Nissen, Ana C.V.E.
AU - Oelgeschlaeger, Michael
AU - Renko, Kostja
AU - Rogiers, Vera
AU - Schüürmann, Gerrit
AU - Stinckens, Evelyn
AU - Stub, Mette H.
AU - Torres-Ruiz, Monica
AU - Van Duursen, Majorie
AU - Vanhaecke, Tamara
AU - Vergauwen, Lucia
AU - Wedebye, Eva Bay
AU - Svingen, Terje
N1 - Publisher Copyright:
Copyright © 2023 Ramhøj, Axelstad, Baert, Cañas-Portilla, Chalmel, Dahmen, De La Vieja, Evrard, Haigis, Hamers, Heikamp, Holbech, Iglesias-Hernandez, Knapen, Marchandise, Morthorst, Nikolov, Nissen, Oelgeschlaeger, Renko, Rogiers, Schüürmann, Stinckens, Stub, Torres-Ruiz, Van Duursen, Vanhaecke, Vergauwen, Wedebye and Svingen.
PY - 2023
Y1 - 2023
N2 - Current test strategies to identify thyroid hormone (TH) system disruptors are inadequate for conducting robust chemical risk assessment required for regulation. The tests rely heavily on histopathological changes in rodent thyroid glands or measuring changes in systemic TH levels, but they lack specific new approach methodologies (NAMs) that can adequately detect TH-mediated effects. Such alternative test methods are needed to infer a causal relationship between molecular initiating events and adverse outcomes such as perturbed brain development. Although some NAMs that are relevant for TH system disruption are available–and are currently in the process of regulatory validation–there is still a need to develop more extensive alternative test batteries to cover the range of potential key events along the causal pathway between initial chemical disruption and adverse outcomes in humans. This project, funded under the Partnership for the Assessment of Risk from Chemicals (PARC) initiative, aims to facilitate the development of NAMs that are specific for TH system disruption by characterizing in vivo mechanisms of action that can be targeted by in embryo/in vitro/in silico/in chemico testing strategies. We will develop and improve human-relevant in vitro test systems to capture effects on important areas of the TH system. Furthermore, we will elaborate on important species differences in TH system disruption by incorporating non-mammalian vertebrate test species alongside classical laboratory rat species and human-derived in vitro assays.
AB - Current test strategies to identify thyroid hormone (TH) system disruptors are inadequate for conducting robust chemical risk assessment required for regulation. The tests rely heavily on histopathological changes in rodent thyroid glands or measuring changes in systemic TH levels, but they lack specific new approach methodologies (NAMs) that can adequately detect TH-mediated effects. Such alternative test methods are needed to infer a causal relationship between molecular initiating events and adverse outcomes such as perturbed brain development. Although some NAMs that are relevant for TH system disruption are available–and are currently in the process of regulatory validation–there is still a need to develop more extensive alternative test batteries to cover the range of potential key events along the causal pathway between initial chemical disruption and adverse outcomes in humans. This project, funded under the Partnership for the Assessment of Risk from Chemicals (PARC) initiative, aims to facilitate the development of NAMs that are specific for TH system disruption by characterizing in vivo mechanisms of action that can be targeted by in embryo/in vitro/in silico/in chemico testing strategies. We will develop and improve human-relevant in vitro test systems to capture effects on important areas of the TH system. Furthermore, we will elaborate on important species differences in TH system disruption by incorporating non-mammalian vertebrate test species alongside classical laboratory rat species and human-derived in vitro assays.
KW - adverse outcome pathways
KW - chemicals
KW - endocrine disruption
KW - non-animal test methods
KW - PARC
KW - regulatory toxicology
KW - thyroid disruption
UR - http://www.scopus.com/inward/record.url?scp=85161015520&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85161015520&partnerID=8YFLogxK
U2 - 10.3389/ftox.2023.1189303
DO - 10.3389/ftox.2023.1189303
M3 - Review article
AN - SCOPUS:85161015520
SN - 2673-3080
VL - 5
SP - 1
EP - 10
JO - Frontiers in Toxicology
JF - Frontiers in Toxicology
M1 - 1189303
ER -