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Cell Population Kinetics and Ploidy Rate of Early Focal Lesions During Hepatocarcinogenesis in the Rat

Overview
Journal Br J Cancer
Specialty Oncology
Date 1989 Dec 1
PMID 2605094
Citations 2
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Abstract

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.

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References
1.
Solt D, Medline A, Farber E . Rapid emergence of carcinogen-induced hyperplastic lesions in a new model for the sequential analysis of liver carcinogenesis. Am J Pathol. 1977; 88(3):595-618. PMC: 2032374. View

2.
Bannasch P, Mayer D, Hacker H . Hepatocellular glycogenosis and hepatocarcinogenesis. Biochim Biophys Acta. 1980; 605(2):217-45. DOI: 10.1016/0304-419x(80)90005-0. View

3.
Schulte-Hermann R, Timmermann-Trosiener I, Schuppler J . Promotion of spontaneous preneoplastic cells in rat liver as a possible explanation of tumor production by nonmutagenic compounds. Cancer Res. 1983; 43(2):839-44. View

4.
Pugh T, Goldfarb S . Quantitative histochemical and autoradiographic studies of hepatocarcinogenesis in rats fed 2-acetylaminofluorene followed by phenobarbital. Cancer Res. 1978; 38(12):4450-7. View

5.
Yager Jr J, POTTER V . A comparison of the effects of 3'-methyl-4-dimethylaminoazobenzene, 2-methyl-4-dimethylaminoazobenzene, and 2-acetylaminofluorene on rat liver DNA stability and new synthesis. Cancer Res. 1975; 35(5):1225-34. View