Published July 10, 2023 | Version v1
Journal article Open

New approach methodologies to facilitate and improve the hazard assessment of non-genotoxic carcinogens—a PARC project

  • 1. INRAE: Toxalim, INRAE, INP-ENVT, INP-EI-Purpan, Université de Toulouse 3 Paul Sabatier, Toulouse, France
  • 2. Department Experimental Toxicology and ZEBET, German Centre for the Protection of Laboratory Animals (Bf3R), German Federal Institute for Risk Assessment, Berlin, Germany
  • 3. Department of Pharmacology and Toxicology, School of Pharmacy and Nutrition, UNAV: University of Navarra, Pamplona, Spain
  • 4. IRFMN: Istituto di Ricerche Farmacologiche Mario Negri—IRCCS, Milan, Italy
  • 5. RECETOX, Faculty of Science, Masaryk University, Brno, Czechia,
  • 6. INSERM UMR-S 1124 T3S — Université Paris Cité, Paris, France
  • 7. UL-LACDR: Leiden Academic Centre for Drug Research, Leiden University, Leiden, Netherlands
  • 8. Department Food Safety, German Federal Institute for Risk Assessment, Berlin, Germany
  • 9. Health Effects Laboratory, NILU: The Climate and Environmental Research Institute, Kjeller, Norway
  • 10. Department of Chemistry, RPTU: Division of Food Chemistry and Toxicology, Kaiserslautern, Germany
  • 11. ANSES: French Agency for Food, Environmental and Occupational Health and Safety, Fougères Laboratory, Toxicology of Contaminants Unit, Fougères, France
  • 12. RIVM: National Institute for Public Health and the Environment, Bilthoven, Netherlands,
  • 13. Radiation, Chemical and Environmental Hazards, UKHSA: UK Health Security Agency, Chilton, Oxfordshire, United Kingdom
  • 14. Department of Genetic Toxicology and Cancer Biology, NIB: National Institute of Biology, Ljubljana, Slovenia

Description

Carcinogenic chemicals, or their metabolites, can be classified as genotoxic or non-genotoxic carcinogens (NGTxCs). Genotoxic compounds induce DNA damage, which can be detected by an established in vitro and in vivo battery of genotoxicity assays. For NGTxCs, DNA is not the primary target, and the possible modes of action (MoA) of NGTxCs are much more diverse than those of genotoxic compounds, and there is no specific in vitro assay for detecting NGTxCs. Therefore, the evaluation of the carcinogenic potential is still dependent on long-term studies in rodents. This 2-year bioassay, mainly applied for testing agrochemicals and pharmaceuticals, is time-consuming, costly and requires very high numbers of animals. More importantly, its relevance for human risk assessment is questionable due to the limited predictivity for human cancer risk, especially with regard to NGTxCs. Thus, there is an urgent need for a transition to new approach methodologies (NAMs), integrating human-relevant in vitro assays and in silico tools that better exploit the current knowledge of the multiple processes involved in carcinogenesis into a modern safety assessment toolbox. Here, we describe an integrative project that aims to use a variety of novel approaches to detect the carcinogenic potential of NGTxCs based on different mechanisms and pathways involved in carcinogenesis. The aim of this project is to contribute suitable assays for the safety assessment toolbox for an efficient and improved, internationally recognized hazard assessment of NGTxCs, and ultimately to contribute to reliable mechanism-based next-generation risk assessment for chemical carcinogens.

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Additional details

Funding

PARC – Partnership for the Assessment of Risks from Chemicals 101057014
European Commission