Your browser doesn't support javascript.
loading
Human relevance of rodent liver tumors: Key insights from a Toxicology Forum workshop on nongenotoxic modes of action.
Felter, Susan P; Foreman, Jennifer E; Boobis, Alan; Corton, J Christopher; Doi, Adriana M; Flowers, Lynn; Goodman, Jay; Haber, Lynne T; Jacobs, Abigail; Klaunig, James E; Lynch, Angela M; Moggs, Jonathan; Pandiri, Arun.
Afiliação
  • Felter SP; Procter and Gamble, Central Product Safety, Mason, OH, United States. Electronic address: Felter.sp@pg.com.
  • Foreman JE; ExxonMobil Biomedical Sciences, Inc., Annandale, NJ, United States.
  • Boobis A; Department of Medicine, Imperial College London, London, UK.
  • Corton JC; National Health and Environmental Effects Research Lab, US EPA, Durham, NC, United States.
  • Doi AM; BASF Corporation, Research Triangle Park, NC, United States.
  • Flowers L; Office of Science Policy, US EPA, Washington DC, United States.
  • Goodman J; Michigan State University, Dept. Pharmacology and Toxicology, East Lansing, MI, United States.
  • Haber LT; Risk Science Center, Dept. of Environmental Health, University of Cincinnati, Cincinnati, OH, United States.
  • Jacobs A; Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD, United States.
  • Klaunig JE; Indiana University, Bloomington, IN, United States.
  • Lynch AM; ToxPlus Consulting, LLC, Haymarket, VA, United States.
  • Moggs J; Novartis Institutes for BioMedical Research, Preclinical Safety, Translational Medicine, Basel, Switzerland.
  • Pandiri A; National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.
Regul Toxicol Pharmacol ; 92: 1-7, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29113941
ABSTRACT
The Toxicology Forum sponsored a workshop in October 2016, on the human relevance of rodent liver tumors occurring via nongenotoxic modes of action (MOAs). The workshop focused on two nuclear receptor-mediated MOAs (Constitutive Androstane Receptor (CAR) and Peroxisome Proliferator Activated Receptor-alpha (PPARα), and on cytotoxicity. The goal of the meeting was to review the state of the science to (1) identify areas of consensus and differences, data gaps and research needs; (2) identify reasons for inconsistencies in current regulatory positions; and (3) consider what data are needed to demonstrate a specific MOA, and when additional research is needed to rule out alternative possibilities. Implications for quantitative risk assessment approaches were discussed, as were implications of not considering MOA and dose in hazard characterization and labeling schemes. Most, but not all, participants considered the CAR and PPARα MOAs as not relevant to humans based on quantitative and qualitative differences. In contrast, cytotoxicity is clearly relevant to humans, but a threshold applies. Questions remain for all three MOAs concerning what data are necessary to determine the MOA and to what extent it is necessary to exclude other MOAs.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hepáticas Tipo de estudo: Etiology_studies / Qualitative_research / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Regul Toxicol Pharmacol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Hepáticas Tipo de estudo: Etiology_studies / Qualitative_research / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Regul Toxicol Pharmacol Ano de publicação: 2018 Tipo de documento: Article
...