Abstract |
Hepatoma cells isolated from rats after administration of a carcinogen, diethylnitrosamine, and propagated in culture, contained a genetically stable cytoskeletal abnormality resembling Mallory bodies. These juxtanuclear aggregates of intermediate-sized filaments were maintained in carcinomas produced in nude mice after inoculation of uncloned mass cultures and a cloned subculture. Paraffin and frozen sections of these tumors revealed acentric nuclei and a glassy hyalin-type cytoplasmic lesion which stained pink with hematoxylin- eosin and blue with Mallory's aniline blue stain. The cells in culture and in the tumor sections were strongly positive for gamma-glutamyl transpeptidase. Cryostat sections examined by indirect immunofluorescence microscopy with antisera to purified bovine hoof prekeratin, desmosome-associated tonofilaments from bovine muzzle, and murine vimentin, as well as transmission electron microscopy revealed the presence of juxtanuclear aggregates of intermediate-sized filaments. All characteristics previously reported for the tissue culture cell line were stably maintained in the tumor tissue. These results suggest that the Mallory body-containing cells frequently observed in man in alcoholic hepatitis and other degenerative liver diseases could, under appropriate environmental "promoting" conditions, be precursor cells in focal hepatocellular carcinoma formation.
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Authors | E Borenfreund, E deHarven, L Garra |
Journal | Hepatology (Baltimore, Md.)
(Hepatology)
1981 Sep-Oct
Vol. 1
Issue 5
Pg. 408-15
ISSN: 0270-9139 [Print] United States |
PMID | 6273281
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Mallory body protein, mouse
- Mallory body protein, rat
- Proteins
- Diethylnitrosamine
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Topics |
- Animals
- Cell Transformation, Neoplastic
- Cells, Cultured
- Diethylnitrosamine
- Female
- Fluorescent Antibody Technique
- Inclusion Bodies
- Liver Neoplasms, Experimental
(chemically induced, ultrastructure)
- Mice
- Mice, Nude
- Microscopy, Electron
- Proteins
- Rats
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