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Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol

Sesamol was administered at a dietary level of 2% to groups of 30 male and female F344/DuCrj rats and B6C3F, mice for 104and 96 weeks, respectively. Squamous cell carcinomas in the forestomach were Induced in nine of 29 (31%) effective male rats, three of 30 (10%) female rats, eleven of 29 (38%) mal...

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Detalles Bibliográficos
Autores principales: Tamano, Seiko, Hirose, Masao, Tanaka, Hikaru, Asakawa, Emiko, Ogawa, Kumiko, Ito, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918737/
https://www.ncbi.nlm.nih.gov/pubmed/1483943
http://dx.doi.org/10.1111/j.1349-7006.1992.tb02759.x
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author Tamano, Seiko
Hirose, Masao
Tanaka, Hikaru
Asakawa, Emiko
Ogawa, Kumiko
Ito, Nobuyuki
author_facet Tamano, Seiko
Hirose, Masao
Tanaka, Hikaru
Asakawa, Emiko
Ogawa, Kumiko
Ito, Nobuyuki
author_sort Tamano, Seiko
collection PubMed
description Sesamol was administered at a dietary level of 2% to groups of 30 male and female F344/DuCrj rats and B6C3F, mice for 104and 96 weeks, respectively. Squamous cell carcinomas in the forestomach were Induced in nine of 29 (31%) effective male rats, three of 30 (10%) female rats, eleven of 29 (38%) male mice and five of 30 (17%) female mice treated with sesamol. Papillomas developed in ten of 29 (34%) male rats and fourteen of 30 (47%) female rats, but not in any of the mice. Hyperplasias developed in almost all rats and mice of both sexes. Significant differences from control values were found for all three lesions in rats and for carcinoma and hyperplasia categories in mice. The incidences of other tumors in the 2% sesamol group were comparable with control values. In conclusion, sesamol induces squamous cell carcinomas in the forestomach of rats and mice, males being more susceptible than females.
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spelling pubmed-59187372018-05-11 Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol Tamano, Seiko Hirose, Masao Tanaka, Hikaru Asakawa, Emiko Ogawa, Kumiko Ito, Nobuyuki Jpn J Cancer Res Article Sesamol was administered at a dietary level of 2% to groups of 30 male and female F344/DuCrj rats and B6C3F, mice for 104and 96 weeks, respectively. Squamous cell carcinomas in the forestomach were Induced in nine of 29 (31%) effective male rats, three of 30 (10%) female rats, eleven of 29 (38%) male mice and five of 30 (17%) female mice treated with sesamol. Papillomas developed in ten of 29 (34%) male rats and fourteen of 30 (47%) female rats, but not in any of the mice. Hyperplasias developed in almost all rats and mice of both sexes. Significant differences from control values were found for all three lesions in rats and for carcinoma and hyperplasia categories in mice. The incidences of other tumors in the 2% sesamol group were comparable with control values. In conclusion, sesamol induces squamous cell carcinomas in the forestomach of rats and mice, males being more susceptible than females. Blackwell Publishing Ltd 1992-12 /pmc/articles/PMC5918737/ /pubmed/1483943 http://dx.doi.org/10.1111/j.1349-7006.1992.tb02759.x Text en
spellingShingle Article
Tamano, Seiko
Hirose, Masao
Tanaka, Hikaru
Asakawa, Emiko
Ogawa, Kumiko
Ito, Nobuyuki
Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title_full Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title_fullStr Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title_full_unstemmed Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title_short Forestomach Neoplasm Induction in F344/DuCrj Rats and B6C3F(1) Mice Exposed to Sesamol
title_sort forestomach neoplasm induction in f344/ducrj rats and b6c3f(1) mice exposed to sesamol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918737/
https://www.ncbi.nlm.nih.gov/pubmed/1483943
http://dx.doi.org/10.1111/j.1349-7006.1992.tb02759.x
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