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A critical review of the acetaminophen preclinical carcinogenicity and tumor promotion data and their implications for its carcinogenic hazard potential.
Murray, F Jay; Monnot, Andrew D; Jacobson-Kram, David; Cohen, Samuel M; Hardisty, Jerry F; Bandara, Suren B; Kovochich, Michael; Deore, Milind; Pitchaiyan, Suresh Kumar; Gelotte, Cathy K; Lai, John C K; Atillasoy, Evren; Hermanowski-Vosatka, Anne; Kuffner, Edwin; Unice, Kenneth M; Yang, Kyunghee; Gebremichael, Yeshitila; Howell, Brett A; Eichenbaum, Gary.
Afiliação
  • Murray FJ; Murray & Associates, San Jose, CA, USA.
  • Monnot AD; Cardno ChemRisk, San Francisco, CA, USA.
  • Jacobson-Kram D; ToxRox Consulting, McLean, VA, USA.
  • Cohen SM; Havlik-Wall Professor of Oncology, Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Hardisty JF; Experimental Pathology Laboratories, Inc., Durham, NC, USA.
  • Bandara SB; Cardno ChemRisk, San Francisco, CA, USA.
  • Kovochich M; Cardno ChemRisk, Chicago, IL, USA.
  • Deore M; Johnson & Johnson Consumer, India.
  • Pitchaiyan SK; Johnson & Johnson Consumer, India.
  • Gelotte CK; Johnson & Johnson Consumer Products, USA.
  • Lai JCK; Johnson & Johnson Consumer Products, USA.
  • Atillasoy E; Johnson & Johnson Consumer Products, USA.
  • Hermanowski-Vosatka A; Johnson & Johnson Consumer Products, USA.
  • Kuffner E; Johnson & Johnson Consumer Products, USA.
  • Unice KM; Cardno ChemRisk, Pittsburgh, PA, USA.
  • Yang K; DILIsym Services Inc., Research Triangle Park, NC, USA.
  • Gebremichael Y; DILIsym Services Inc., Research Triangle Park, NC, USA.
  • Howell BA; DILIsym Services Inc., Research Triangle Park, NC, USA.
  • Eichenbaum G; Johnson & Johnson, New Brunswick, NJ, USA. Electronic address: geichenb@its.jnj.com.
Regul Toxicol Pharmacol ; 118: 104801, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33039518
ABSTRACT
In 2019 the California Office of Environmental Health Hazard Assessment (OEHHA) initiated a review of the carcinogenic hazard potential of acetaminophen, including an assessment of the long-term rodent carcinogenicity and tumor initiation/promotion studies. The objective of the analysis herein was to inform this review process with a weight-of-evidence assessment of these studies and an assessment of the relevance of these models to humans. In most of the 14 studies, there were no increases in the incidences of tumors in any organ system. In the few studies in which an increase in tumor incidence was observed, there were factors such as absence of a dose response and a rodent-specific tumor supporting that these findings are not relevant to human hazard identification. In addition, we performed qualitative analysis and quantitative simulations of the exposures to acetaminophen and its metabolites and its toxicity profile; the data support that the rodent models are toxicologically relevant to humans. The preclinical carcinogenicity results are consistent with the broader weight of evidence assessment and evaluations of multiple international health authorities supporting that acetaminophen is not a carcinogenic hazard.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes de Carcinogenicidade / Transformação Celular Neoplásica / Analgésicos não Narcóticos / Acetaminofen / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Testes de Carcinogenicidade / Transformação Celular Neoplásica / Analgésicos não Narcóticos / Acetaminofen / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article