Literature DB >> 8013421

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

B I Ghanayem1, I M Sanchez, R R Maronpot, M R Elwell, H B Matthews.   

Abstract

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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Year:  1993        PMID: 8013421      PMCID: PMC1519444          DOI: 10.1289/ehp.93101s5277

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  14 in total

Review 1.  Genetic errors, cell proliferation, and carcinogenesis.

Authors:  S M Cohen; L B Ellwein
Journal:  Cancer Res       Date:  1991-12-15       Impact factor: 12.701

2.  Sustainability of forestomach hyperplasia in rats treated with ethyl acrylate for 13 weeks and regression after cessation of dosing.

Authors:  B I Ghanayem; H B Matthews; R R Maronpot
Journal:  Toxicol Pathol       Date:  1991       Impact factor: 1.902

3.  Genotoxic effects of ethyl acrylate and methyl acrylate in the mouse evaluated by the micronucleus test.

Authors:  B Przybojewska; E Dziubałtowska; Z Kowalski
Journal:  Mutat Res       Date:  1984-03       Impact factor: 2.433

4.  Association of chemically induced forestomach cell proliferation and carcinogenesis.

Authors:  B I Ghanayem; R R Maronpot; H B Matthews
Journal:  Cancer Lett       Date:  1986-09       Impact factor: 8.679

5.  Relationship of hepatic peroxisome proliferation and replicative DNA synthesis to the hepatocarcinogenicity of the peroxisome proliferators di(2-ethylhexyl)phthalate and [4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio]acetic acid (Wy-14,643) in rats.

Authors:  D S Marsman; R C Cattley; J G Conway; J A Popp
Journal:  Cancer Res       Date:  1988-12-01       Impact factor: 12.701

6.  Comparison of the effects of 13 phenolic compounds in induction of proliferative lesions of the forestomach and increase in the labelling indices of the glandular stomach and urinary bladder epithelium of Syrian golden hamsters.

Authors:  M Hirose; T Inoue; M Asamoto; Y Tagawa; N Ito
Journal:  Carcinogenesis       Date:  1986-08       Impact factor: 4.944

7.  Ethyl acrylate-induced gastric toxicity. III. Development and recovery of lesions.

Authors:  B I Ghanayem; R R Maronpot; H B Matthews
Journal:  Toxicol Appl Pharmacol       Date:  1986-05       Impact factor: 4.219

8.  A carcinogenesis reversibility study of the effects of butylated hydroxyanisole on the forestomach and urinary bladder in male Fischer 344 rats.

Authors:  E A Nera; F Iverson; E Lok; C L Armstrong; K Karpinski; D B Clayson
Journal:  Toxicology       Date:  1988-12-30       Impact factor: 4.221

9.  Ethyl acrylate-induced gastric toxicity. I. Effect of single and repetitive dosing.

Authors:  B I Ghanayem; R R Maronpot; H B Matthews
Journal:  Toxicol Appl Pharmacol       Date:  1985-09-15       Impact factor: 4.219

10.  Ethyl acrylate-induced gastric toxicity. II. Structure-toxicity relationships and mechanism.

Authors:  B I Ghanayem; R R Maronpot; H B Matthews
Journal:  Toxicol Appl Pharmacol       Date:  1985-09-15       Impact factor: 4.219

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  3 in total

1.  Proportionate cancer mortality in methyl methacrylate-exposed orthopedic surgeons compared to general surgeons.

Authors:  James Henry Diaz
Journal:  J Med Toxicol       Date:  2011-06

Review 2.  Chemical carcinogenesis of the gastrointestinal tract in rodents: an overview with emphasis on NTP carcinogenesis bioassays.

Authors:  Sundeep A Chandra; Michael W Nolan; David E Malarkey
Journal:  Toxicol Pathol       Date:  2009-12-17       Impact factor: 1.902

3.  Cell Proliferation and Chemical Carcinogenesis: summary and future directions.

Authors:  J A Swenberg
Journal:  Environ Health Perspect       Date:  1993-12       Impact factor: 9.031

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