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Chemical carcinogen safety testing: OECD expert group international consensus on the development of an integrated approach for the testing and assessment of chemical non-genotoxic carcinogens

Zugehörigkeit
Centre for Radiation, Chemical and Environmental Hazards (CRCE), Public Health England, Chilton, United Kingdom
Jacobs, Miriam N.;
Zugehörigkeit
Center for Environment, Prevention and Health, Regional Agency for Prevention, Environment and Energy Emilia Romagna Region (Arpae), Bologna, Italy
Colacci, Annamaria;
Zugehörigkeit
European Commission Joint Research Centre (EC JRC), Ispra, Italy
Corvi, Raffaella;
Zugehörigkeit
Center for Environment, Prevention and Health, Regional Agency for Prevention, Environment and Energy Emilia Romagna Region (Arpae), Bologna, Italy
Vaccari, Monica;
Zugehörigkeit
US Food and Drug Administration (FDA), Silver Spring, United States
Aguila, M. Cecilia;
Zugehörigkeit
Corteva Agriscience, Abingdon, United Kingdom
Corvaro, Marco;
Zugehörigkeit
Organisation for Economic Cooperation and Development (OECD), Paris, France
Delrue, Nathalie;
Zugehörigkeit
Health Canada, Ottawa, Canada
Desaulniers, Daniel;
Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Department 9 Experimental Toxicology and ZEBET, Unit 93 Animal Protection and Laboratory Animal Science, Germany
Ertych, Norman;
Zugehörigkeit
US Food and Drug Administration (FDA), Silver Spring, United States
Jacobs, Abigail;
Zugehörigkeit
National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands
Luijten, Mirjam;
Zugehörigkeit
European Commission Joint Research Centre (EC JRC), Ispra, Italy
Madia, Federica;
Zugehörigkeit
National Institute of Health Sciences, Kawasaki, Japan
Nishikawa, Akiyoshi;
Zugehörigkeit
National Institute of Health Sciences, Kawasaki, Japan
Ogawa, Kumiko;
Zugehörigkeit
Kanagawa Prefectural Institute of Public Health, Chigasaki, Japan
Ohmori, Kiyomi;
Zugehörigkeit
Division of Medical Biochemistry, Biocenter, Medical University of Innsbruck, Innsbruck, Austria
Paparella, Martin;
Zugehörigkeit
Technical University of Denmark, Lyngby, Denmark
Sharma, Anoop Kumar;
Zugehörigkeit
CNRS University de Lorraine, Lorraine, France
Vasseur, Paule

While regulatory requirements for carcinogenicity testing of chemicals vary according to product sector and regulatory jurisdiction, the standard approach starts with a battery of genotoxicity tests (which include mutagenicity assays). If any of the in vivo genotoxicity tests are positive, a lifetime rodent cancer bioassay may be requested, but under most chemical regulations (except plant protection, biocides, pharmaceuticals), this is rare. The decision to conduct further testing based on genotoxicity test outcomes creates a regulatory gap for the identification of non-genotoxic carcinogens (NGTxC). With the objective of addressing this gap, in 2016, the Organization of Economic Cooperation and Development (OECD) established an expert group to develop an integrated approach to the testing and assessment (IATA) of NGTxC. Through that work, a definition of NGTxC in a regulatory context was agreed. Using the adverse outcome pathway (AOP) concept, various cancer models were developed, and overarching mechanisms and modes of action were identified. After further refining and structuring with respect to the common hallmarks of cancer and knowing that NGTxC act through a large variety of specific mechanisms, with cell proliferation commonly being a unifying element, it became evident that a panel of tests covering multiple biological traits will be needed to populate the IATA. Consequently, in addition to literature and database investigation, the OECD opened a call for relevant assays in 2018 to receive suggestions. Here, we report on the definition of NGTxC, on the development of the overarching NGTxC IATA, and on the development of ranking parameters to evaluate the assays. Ultimately the intent is to select the best scoring assays for integration in an NGTxC IATA to better identify carcinogens and reduce public health hazards.

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