A Review of the Hepatic Tumors Related to Mixed-Function Oxidase Induction in the Mouse
Open Access
- 1 July 1996
- journal article
- review article
- Published by SAGE Publications in Toxicologic Pathology
- Vol. 24 (4) , 484-492
- https://doi.org/10.1177/019262339602400411
Abstract
Mixed-function oxidase (MFO) induction in the mouse liver results in a rapid and sustained centrilobular hypertrophy associated with a hyperplastic response. In many studies, the long-term sequela of prolonged exposure is an increased incidence of lesions considered to be adenomas. Studies have shown in aged control mice that the burden of adenomas usually consists of lesions with basophilic cytoplasic staining and a uniform population of hepatocyte nuclei. With long-term feeding of MFO inducers, there is an additional burden of lesions diagnosed as adenomas having a different histological appearance with increased eosinophilic cytoplasm and pleomorphic nuclei. The incidence of hepatocarcinomas usually is not modified by the increased incidence of eosinophilic adenomas. Studies into the behavior of the eosinophilic lesions show that the hepatocytes approximate in their behavior to normal and not neoplastic cells. It is suggested that these lesions should not be considered a carcinogenic response to the chemical.Keywords
This publication has 24 references indexed in Scilit:
- Hepatocarcinogenicity of chlordane in B6C3F1 and B6D2F1 male mice: evidence for regression in B6C3F1 mice and carcinogenesis independent of ras proto-oncogene activationCarcinogenesis: Integrative Cancer Research, 1995
- Mutations in the ras proto-oncogene: clues to etiology and molecular pathogenesis of mouse liver tumorsToxicology, 1995
- Dose-dependent ras mutation spectra in N-nitrosodiethylamine induced mouse liver tumors and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone induced mouse lung tumorsCarcinogenesis: Integrative Cancer Research, 1993
- Cloning of the Ah-receptor cDNA reveals a distinctive ligand-activated transcription factor.Proceedings of the National Academy of Sciences, 1992
- Cloning of a Factor Required for Activity of the Ah (Dioxin) ReceptorScience, 1991
- The Histopathology and Biochemistry of Phenobarbitone-Induced Liver Nodules in C3H MicePublished by Springer Nature ,1987
- The histology and development of hepatic nodules in C3H/He mice following chronic administration of phenobarbitoneCarcinogenesis: Integrative Cancer Research, 1986
- Sustained induction of hepatic xenobiotic metabolising enzyme activities by phenobarbitone in C3H/He mice: Relevance to nodule formationToxicology, 1984
- Zonal changes in the rat liver after chronic administration of phenobarbitone: An ultrastructural, morphometric and biochemical correlationChemico-Biological Interactions, 1979
- Histochemical observations on nodules induced in the mouse liver by phenobarbitoneThe Journal of Pathology, 1978