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Pathogenesis of chemically induced nasal cavity tumors in rodents: contribution to adverse outcome pathway.
Nishikawa, Akiyoshi; Nagano, Kasuke; Kojima, Hajime; Fukushima, Shoji; Ogawa, Kumiko.
Afiliação
  • Nishikawa A; Division of Pathology, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-shi, Kanagawa 210-9501, Japan.
  • Nagano K; Division of Clinical Pathology, Nagoya Tokushukai General Hospital, 2-52 Kouzoji-cho kita, Kasugai-shi, Aichi 487-0016, Japan.
  • Kojima H; Nagano Toxicologic-Pathology Consulting, 467-7 Ojiri, Hadano-shi, Kanagawa 257-0011, Japan.
  • Fukushima S; Division of Risk Assessment, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-shi, Kanagawa 210-9501, Japan.
  • Ogawa K; Association for Promotion of Research on Risk Assessment, 1-134 Arako, Nakagawa-ku, Nagoya 454-0869, Japan.
J Toxicol Pathol ; 37(1): 11-27, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38283373
ABSTRACT
The pathogenesis of nasal cavity tumors induced in rodents has been critically reviewed. Chemical substances that induce nasal cavity tumors in rats, mice, and hamsters were searched in the National Toxicology Program (NTP), International Agency for Research on Cancer (IARC), and Japan Bioassay Research Center (JBRC) databases, in addition to PubMed. Detailed data such as animal species, administration routes, and histopathological types were extracted for induced nasal cavity tumors. Data on non-neoplastic lesions were also extracted. The relationship between the tumor type and non-neoplastic lesions at equivalent sites was analyzed to evaluate tumor pathogenesis. Genotoxicity data were also analyzed. Squamous cell carcinoma was the most frequent lesion, regardless of the dosing route, and its precursor lesions were squamous metaplasia and/or respiratory epithelial hyperplasia, similar to squamous cell papilloma. The precursor lesions of adenocarcinoma, the second most frequent tumor type, were mainly olfactory epithelial hyperplasia, whereas those of adenoma were respiratory epithelial lesions. These pathways were consistent among species. Our results suggest that the responsible lesions may be commonly linked with chemically-induced cytotoxicity in each tumor type, irrespective of genotoxicity, and that the pathways may largely overlap between genotoxic and non-genotoxic carcinogens. These findings may support the documentation of adverse outcome pathways (AOPs), such as cytotoxicity, leading to nasal cavity tumors and the integrated approaches to testing and assessment (IATA) for non-genotoxic carcinogens.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Ano de publicação: 2024 Tipo de documento: Article