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The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment

Medication with L-thyroxine or methylthiouracil of castrate rats painted weekly 5, 10, 20 or 40 times with DMBA does not alter the order of thresholds for carcinogenesis which increases from that for cervico-vaginal epitheliomas via squamous celled and basal celled vulval tumours to cervicovaginal s...

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Autores principales: Glucksmann, A., Cherry, Cora P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1970
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008733/
https://www.ncbi.nlm.nih.gov/pubmed/5503602
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author Glucksmann, A.
Cherry, Cora P.
author_facet Glucksmann, A.
Cherry, Cora P.
author_sort Glucksmann, A.
collection PubMed
description Medication with L-thyroxine or methylthiouracil of castrate rats painted weekly 5, 10, 20 or 40 times with DMBA does not alter the order of thresholds for carcinogenesis which increases from that for cervico-vaginal epitheliomas via squamous celled and basal celled vulval tumours to cervicovaginal sarcomas. Methylthiouracil lowers the threshold for basal celled vulval neoplasms. Sarcomas reach a peak of 25% with 20 doses of DMBA in non-medicated rats, but rise to 90% and at a faster rate in animals given either of the thyroactive drugs with further carcinogenic treatment. The optimal dose phenomenon for cervico-vaginal epitheliomas, i.e. a significant fall with continued painting from a peak reached by 5 to 20 doses of DMBA, is not affected by medication with methylthiouracil or L-thyroxine. Thyroactive compounds accelerate the formation of squamous celled vulval tumours which reach a maximum with 20 DMBA paintings; the total incidence as well as the proportion of carcinomas to papillomas falls with further treatment. Methylthiouracil promotes formation of basal celled vulval tumours at low dose levels, but inhibits it at the highest. In medicated as in non-medicated rats the induction of basal celled tumours of the vulva follows an optimum dose pattern. The optimal dose phenomenon and the effect of thyroactive compounds on the tissue-specific sensitivity to carcinogens are discussed. IMAGES:
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spelling pubmed-20087332009-09-10 The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment Glucksmann, A. Cherry, Cora P. Br J Cancer Articles Medication with L-thyroxine or methylthiouracil of castrate rats painted weekly 5, 10, 20 or 40 times with DMBA does not alter the order of thresholds for carcinogenesis which increases from that for cervico-vaginal epitheliomas via squamous celled and basal celled vulval tumours to cervicovaginal sarcomas. Methylthiouracil lowers the threshold for basal celled vulval neoplasms. Sarcomas reach a peak of 25% with 20 doses of DMBA in non-medicated rats, but rise to 90% and at a faster rate in animals given either of the thyroactive drugs with further carcinogenic treatment. The optimal dose phenomenon for cervico-vaginal epitheliomas, i.e. a significant fall with continued painting from a peak reached by 5 to 20 doses of DMBA, is not affected by medication with methylthiouracil or L-thyroxine. Thyroactive compounds accelerate the formation of squamous celled vulval tumours which reach a maximum with 20 DMBA paintings; the total incidence as well as the proportion of carcinomas to papillomas falls with further treatment. Methylthiouracil promotes formation of basal celled vulval tumours at low dose levels, but inhibits it at the highest. In medicated as in non-medicated rats the induction of basal celled tumours of the vulva follows an optimum dose pattern. The optimal dose phenomenon and the effect of thyroactive compounds on the tissue-specific sensitivity to carcinogens are discussed. IMAGES: Nature Publishing Group 1970-12 /pmc/articles/PMC2008733/ /pubmed/5503602 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Articles
Glucksmann, A.
Cherry, Cora P.
The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title_full The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title_fullStr The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title_full_unstemmed The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title_short The Effect of Thyroactive Substances on the Induction of Cervico-vaginal and Vulval Tumours in Castrate Rats at Various Levels of Carcinogenic Treatment
title_sort effect of thyroactive substances on the induction of cervico-vaginal and vulval tumours in castrate rats at various levels of carcinogenic treatment
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008733/
https://www.ncbi.nlm.nih.gov/pubmed/5503602
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