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Prohibitin expression is decreased in the regenerating liver but not in chemically induced hepatic tumors in rats.
- Source :
-
Japanese journal of cancer research : Gann [Jpn J Cancer Res] 1997 Dec; Vol. 88 (12), pp. 1155-64. - Publication Year :
- 1997
-
Abstract
- Expression of prohibition, a growing-regulatory protein, was immunohistochemically investigated in normal rat tissues, regenerating livers, and chemically induced preneoplastic and neoplastic hepatic lesions. Specific cell types including hepatocytes, striated and smooth muscle cells, salivary gland duct epithelial cells, chondrocytes, immature spermatocytes and oocytes were found to be positive. In regenerating livers, prohibitin protein disappeared as early as 3 h after two-thirds hepatectomy and returned to near the original level by 24 h, while its mRNA level did not markedly vary. The timing of the disappearance was coincident with the expression of c-myc, suggesting a relation to quiescent hepatocytes entering the cell cycle. However, no pronounced decrease was evident in the most hyperplastic hepatic nodules and hepatocellular carcinomas investigated. Examination of 9 rat hepatocellular carcinoma cell lines, 6 hyperplastic hepatic nodules and 5 hepatocellular carcinomas revealed a single case of a base substitution in prohibition cDNA, identified as a synonymous sense change. The observed abundant expression of prohibitin in quiescent hepatocytes and its rapid loss under conditions of regeneration indicate a growth-regulatory function, but our results do not suggest any critical role in rat hepatocarcinogenesis.
- Subjects :
- Animals
Carcinogens
Diethylnitrosamine
Female
Immunohistochemistry
Liver metabolism
Liver Neoplasms, Experimental chemically induced
Liver Neoplasms, Experimental pathology
Male
Point Mutation
Prohibitins
Proteins genetics
RNA, Messenger metabolism
Rats
Rats, Inbred F344
Liver drug effects
Liver Neoplasms, Experimental metabolism
Liver Regeneration
Proteins metabolism
Repressor Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 0910-5050
- Volume :
- 88
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Japanese journal of cancer research : Gann
- Publication Type :
- Academic Journal
- Accession number :
- 9473733
- Full Text :
- https://doi.org/10.1111/j.1349-7006.1997.tb00344.x