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Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat.
We have studied the changes in cell population kinetics and DNA-content of cycling parenchymal cells during the very early steps of rat hepatocarcinogenesis in Faber's protocol. Adult rats were initiated by a single dose of diethylnitrosamine (DENA, 200 mg kg-1), followed 2 weeks later by a 2-w...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247254/ https://www.ncbi.nlm.nih.gov/pubmed/2605094 |
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author | Castelain, P. Deleener, A. Kirsch-Volders, M. Barbason, H. |
author_facet | Castelain, P. Deleener, A. Kirsch-Volders, M. Barbason, H. |
author_sort | Castelain, P. |
collection | PubMed |
description | We have studied the changes in cell population kinetics and DNA-content of cycling parenchymal cells during the very early steps of rat hepatocarcinogenesis in Faber's protocol. Adult rats were initiated by a single dose of diethylnitrosamine (DENA, 200 mg kg-1), followed 2 weeks later by a 2-week diet of 0.03% 2-acetylaminofluorene (2-AAF) as selection phase. In the middle of selection time, a single necrogenic dose of carbon tetrachloride (CCl4, 2 ml kg-1) was administered by gavage. Twenty four hours thereafter, radiolabelled thymidine (3H-TdR, 1.5 microCi g-1) was given by repeated injections during 24 h. An emergence of small, pyroninophilic ('tigroid') foci was observed at the second, fifth and eighth days after the proliferative stimulus. The focal putative precancerous cells presented a significant higher labelling index (L1) than the non-affected parenchymal cells for all exposure times. However, the labelling intensity decreased from the second to the eighth day after CCl4, suggesting a dilution of the radiolabelled DNA by repeated divisions within the foci. The nuclei of the same foci were analysed for DNA-content by feulgen microdensitometry on neighbouring sections. A gradual reduction of nuclear DNA-content was observed in 66% of the foci at the fifth day and in 100% of foci at the eight day, as compared to surrounding tissue and untreated animals, where labelling and DNA-content remain in the same ratio. |
format | Text |
id | pubmed-2247254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22472542009-09-10 Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. Castelain, P. Deleener, A. Kirsch-Volders, M. Barbason, H. Br J Cancer Research Article We have studied the changes in cell population kinetics and DNA-content of cycling parenchymal cells during the very early steps of rat hepatocarcinogenesis in Faber's protocol. Adult rats were initiated by a single dose of diethylnitrosamine (DENA, 200 mg kg-1), followed 2 weeks later by a 2-week diet of 0.03% 2-acetylaminofluorene (2-AAF) as selection phase. In the middle of selection time, a single necrogenic dose of carbon tetrachloride (CCl4, 2 ml kg-1) was administered by gavage. Twenty four hours thereafter, radiolabelled thymidine (3H-TdR, 1.5 microCi g-1) was given by repeated injections during 24 h. An emergence of small, pyroninophilic ('tigroid') foci was observed at the second, fifth and eighth days after the proliferative stimulus. The focal putative precancerous cells presented a significant higher labelling index (L1) than the non-affected parenchymal cells for all exposure times. However, the labelling intensity decreased from the second to the eighth day after CCl4, suggesting a dilution of the radiolabelled DNA by repeated divisions within the foci. The nuclei of the same foci were analysed for DNA-content by feulgen microdensitometry on neighbouring sections. A gradual reduction of nuclear DNA-content was observed in 66% of the foci at the fifth day and in 100% of foci at the eight day, as compared to surrounding tissue and untreated animals, where labelling and DNA-content remain in the same ratio. Nature Publishing Group 1989-12 /pmc/articles/PMC2247254/ /pubmed/2605094 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 | Research Article Castelain, P. Deleener, A. Kirsch-Volders, M. Barbason, H. Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title | Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title_full | Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title_fullStr | Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title_full_unstemmed | Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title_short | Cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
title_sort | cell population kinetics and ploidy rate of early focal lesions during hepatocarcinogenesis in the rat. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247254/ https://www.ncbi.nlm.nih.gov/pubmed/2605094 |
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