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Origin of the TTC values for compounds that are genotoxic and/or carcinogenic and an approach for their re-evaluation.
Boobis, Alan; Brown, Paul; Cronin, Mark Timothy David; Edwards, James; Galli, Corrado Lodovico; Goodman, Jay; Jacobs, Abigail; Kirkland, David; Luijten, Mirjam; Marsaux, Cyril; Martin, Matthew; Yang, Chihae; Hollnagel, Heli Miriam.
Afiliação
  • Boobis A; a Department of Medicine , Imperial College London , London , UK.
  • Brown P; b US Food and Drug Administration , Silver Spring , MD , USA.
  • Cronin MTD; c School of Pharmacy and Biomolecular Sciences , Liverpool John Moores University , Liverpool , UK.
  • Edwards J; d DSM Nutritional Products Ltd , Kaiseraugst , Switzerland.
  • Galli CL; e Department of Pharmacological and Biomolecular Sciences , University of Milan , Milan , Italy.
  • Goodman J; f Department of Pharmacology and Toxicology , Michigan State University , East Lansing , MI , USA.
  • Jacobs A; b US Food and Drug Administration , Silver Spring , MD , USA.
  • Kirkland D; g Kirkland Consulting , Tadcaster , UK.
  • Luijten M; h Centre for Health Protection , National Institute for Public Health and the Environment (RIVM) , Bilthoven , The Netherlands.
  • Marsaux C; i ILSI Europe a.i.s.b.l. , Brussels , Belgium.
  • Martin M; j Environmental Protection Agency , Washington , DC , USA.
  • Yang C; k Chemical and Biomolecular Engineering , The Ohio State University , Columbus , OH , USA.
  • Hollnagel HM; l Molecular Networks GmbH , Nürnberg , Germany.
Crit Rev Toxicol ; 47(8): 705-727, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28510487
ABSTRACT
The threshold of toxicological concern (TTC) approach is a resource-effective de minimis method for the safety assessment of chemicals, based on distributional analysis of the results of a large number of toxicological studies. It is being increasingly used to screen and prioritize substances with low exposure for which there is little or no toxicological information. The first step in the approach is the identification of substances that may be DNA-reactive mutagens, to which the lowest TTC value is applied. This TTC value was based on the analysis of the cancer potency database and involved a number of assumptions that no longer reflect the state-of-the-science and some of which were not as transparent as they could have been. Hence, review and updating of the database is proposed, using inclusion and exclusion criteria reflecting current knowledge. A strategy for the selection of appropriate substances for TTC determination, based on consideration of weight of evidence for genotoxicity and carcinogenicity is outlined. Identification of substances that are carcinogenic by a DNA-reactive mutagenic mode of action and those that clearly act by a non-genotoxic mode of action will enable the protectiveness to be determined of both the TTC for DNA-reactive mutagenicity and that applied by default to substances that may be carcinogenic but are unlikely to be DNA-reactive mutagens (i.e. for Cramer class I-III compounds). Critical to the application of the TTC approach to substances that are likely to be DNA-reactive mutagens is the reliability of the software tools used to identify such compounds. Current methods for this task are reviewed and recommendations made for their application.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Carcinógenos / Bases de Dados de Compostos Químicos / Mutagênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Crit Rev Toxicol Assunto da revista: TOXICOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Carcinógenos / Bases de Dados de Compostos Químicos / Mutagênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Crit Rev Toxicol Assunto da revista: TOXICOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido