LIVER CARCINOGENESIS ASSOCIATED WITH FEEDING OF ETHIONINE IN A CHOLINE-FREE DIET - EVIDENCE AGAINST A ROLE OF OVAL CELLS IN THE EMERGENCE OF HEPATOCELLULAR-CARCINOMA

Citation
F. Tarsetti et al., LIVER CARCINOGENESIS ASSOCIATED WITH FEEDING OF ETHIONINE IN A CHOLINE-FREE DIET - EVIDENCE AGAINST A ROLE OF OVAL CELLS IN THE EMERGENCE OF HEPATOCELLULAR-CARCINOMA, Hepatology, 18(3), 1993, pp. 596-603
Citations number
47
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
ISSN journal
02709139
Volume
18
Issue
3
Year of publication
1993
Pages
596 - 603
Database
ISI
SICI code
0270-9139(1993)18:3<596:LCAWFO>2.0.ZU;2-S
Abstract
In an attempt to clarify the role of oval cells in the emergence of he patocellular carcinoma, we fed rats a choline-free diet containing 0%, 0.05% or 0.1% ethionine. The incidence and nature of premalignant and malignant hepatic lesions were then related to the degree of oval cel l proliferation. Intake of choline-free diet alone for up to 12 mo was associated with minimal oval cell proliferation; cholangiofibrosis, h epatocellular nodules and hepatocellular carcinoma were observed in 55 %, 23% and 14% of the animals, respectively. When rats were given the choline-free diet with 0.05% ethionine, proliferation of oval cells wa s more pronounced; after a 6- to 12 mo feeding period, cholangiofibros is (57%) was again observed. However, hepatocellular nodules (91%) and hepatocellular carcinoma (74%) were the most common lesions seen with this feeding regimen. Finally, rats fed the choline-free diet with 0. 1% ethionine had massive oval cell proliferation and progressive loss of parenchymal liver tissue. Most of these animals died before they ha d consumed the choline-free diet with 0.1% ethionine for 12 mo. Rats i n this group (96%) exhibited large and numerous cholangiofibrotic lesi ons, but hepatocellular nodules and carcinoma were not detected. In al l animals of each experimental group, hyperplastic bile duct cells in areas of cholangiofibrosis and oval cells were positive for cytokerati n 19, an intermediate filament protein present only in bile duct cells in normal liver. Hepatocellular nodules and hepatocellular carcinoma were invariably negative for cytokeratin 19. We interpret these findin gs to suggest that oval cells are not involved in the histogenesis of hepatocellular carcinoma. They are, rather, consistent with the view t hat hepatocellular carcinoma is hepatocellular in lineage in hepatocar cinogenesis during intake of a choline-free diet (whether or not it is supplemented with ethionine) and, possibly, in other forms of neoplas tic liver growth associated with oval cell proliferation.