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Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.

Chronic administration of ethyl acrylate (EA) by gavage at 100 or 200 mg/kg/day resulted in a significant dose-dependent increase in the incidence of forestomach (FS) squamous cell papillomas and carcinomas in both sexes of F344 rats and B6C3F1 mice. Subsequent work in this laboratory was designed t...

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Detalles Bibliográficos
Autores principales: Ghanayem, B I, Sanchez, I M, Maronpot, R R, Elwell, M R, Matthews, H B
Formato: Texto
Lenguaje:English
Publicado: 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1519444/
https://www.ncbi.nlm.nih.gov/pubmed/8013421
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author Ghanayem, B I
Sanchez, I M
Maronpot, R R
Elwell, M R
Matthews, H B
author_facet Ghanayem, B I
Sanchez, I M
Maronpot, R R
Elwell, M R
Matthews, H B
author_sort Ghanayem, B I
collection PubMed
description Chronic administration of ethyl acrylate (EA) by gavage at 100 or 200 mg/kg/day resulted in a significant dose-dependent increase in the incidence of forestomach (FS) squamous cell papillomas and carcinomas in both sexes of F344 rats and B6C3F1 mice. Subsequent work in this laboratory was designed to investigate the relationship between EA-induced FS hyperplasia and carcinogenicity. Current studies have focused on determining the time required for sustained FS hyperplasia to produce neoplastic transformation. Results of these studies demonstrated that gavage administration of EA to male F344 rats at 200 mg/kg/day for 6 or 12 months caused a sustained increase in FS epithelial hyperplasia for as long as exposure to EA continued. However, FS hyperplasia regressed, and no neoplasms developed when animals receiving EA for 6 months were allowed to recover until they were sacrificed at 24 months of age. In contrast, rats treated for 12 months and allowed 9 months recovery developed FS squamous cell carcinomas (3/13) and papillomas (1/13) for a combined incidence of 4/13. No gross lesions were detected in the liver of any of the rats treated with EA or corn oil vehicle, confirming the tissue specificity in the relationship between EA-induced FS hyperplasia and carcinogenesis. In conclusion, the present work has demonstrated that FS hyperplasia is selectively sustained at the site of EA-induced carcinogenicity for as long as EA is administered and has also demonstrated a temporal relationship between FS mucosal hyperplasia and the development of FS neoplasia by EA.(ABSTRACT TRUNCATED AT 250 WORDS)
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spelling pubmed-15194442006-07-26 Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity. Ghanayem, B I Sanchez, I M Maronpot, R R Elwell, M R Matthews, H B Environ Health Perspect Research Article Chronic administration of ethyl acrylate (EA) by gavage at 100 or 200 mg/kg/day resulted in a significant dose-dependent increase in the incidence of forestomach (FS) squamous cell papillomas and carcinomas in both sexes of F344 rats and B6C3F1 mice. Subsequent work in this laboratory was designed to investigate the relationship between EA-induced FS hyperplasia and carcinogenicity. Current studies have focused on determining the time required for sustained FS hyperplasia to produce neoplastic transformation. Results of these studies demonstrated that gavage administration of EA to male F344 rats at 200 mg/kg/day for 6 or 12 months caused a sustained increase in FS epithelial hyperplasia for as long as exposure to EA continued. However, FS hyperplasia regressed, and no neoplasms developed when animals receiving EA for 6 months were allowed to recover until they were sacrificed at 24 months of age. In contrast, rats treated for 12 months and allowed 9 months recovery developed FS squamous cell carcinomas (3/13) and papillomas (1/13) for a combined incidence of 4/13. No gross lesions were detected in the liver of any of the rats treated with EA or corn oil vehicle, confirming the tissue specificity in the relationship between EA-induced FS hyperplasia and carcinogenesis. In conclusion, the present work has demonstrated that FS hyperplasia is selectively sustained at the site of EA-induced carcinogenicity for as long as EA is administered and has also demonstrated a temporal relationship between FS mucosal hyperplasia and the development of FS neoplasia by EA.(ABSTRACT TRUNCATED AT 250 WORDS) 1993-12 /pmc/articles/PMC1519444/ /pubmed/8013421 Text en
spellingShingle Research Article
Ghanayem, B I
Sanchez, I M
Maronpot, R R
Elwell, M R
Matthews, H B
Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title_full Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title_fullStr Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title_full_unstemmed Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title_short Relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
title_sort relationship between the time of sustained ethyl acrylate forestomach hyperplasia and carcinogenicity.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1519444/
https://www.ncbi.nlm.nih.gov/pubmed/8013421
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