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ID 30772
JaLCDOI
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Author
Pu, Hong
Tsuji, Toshiya
Kondo, Asami
Fushimi, Kazuo
Ohashi, Ryuichiro
Inoue, Yusuke
Mimura, Tetsushige
Hamazaki, Keisuke
Miyazaki, Masahiro
Namba, Masayoshi
Abstract

Characteristics of human hepatoma cell lines with the wild-type p53 were compared with those of human hepatoma cell lines with the mutant-type p53. The p21 protein located downstream of p53 was expressed in cell lines with the wild-type p53 but was not expressed in cell lines with the mutant-type p53. As to other tumor suppressor genes such as p16 and p27, there was no difference in their expression between both types of cell lines. In addition, no marked difference was observed in the activities of CDK2 and CDK4 between cell lines with the wild-type and the mutant-type p53. Phosphorylated Rb protein was detected in all cell lines except the HLE line, indicating that this cell line may have a deletion of and/or a mutation of the Rb gene. These results indicate that abnormalities of tumor suppressor genes other than p53, p16, p27, and Rb may be involved in hepatocarcinogenesis. The population doubling time of the wild-type p53 cells was significantly longer than that of the mutant p53 cells. Neither type of cell line showed a specific chromosome distribution which would indicate karyotype instability. The cell lines expressing the wild-type p53 produced tumors at lower frequency than those with the mutant p53 gene. Although there was no significant difference in effects of TGF-β1, EGF, cholera toxin, and db-cAMP on cell growth between the two types of cells, all three cell lines with the wild-type p53 were resistant to cytotoxicity of TNF-α, while two of the three with the mutant p53 were very sensitive to its cytotoxic effects.

Keywords
hepatoma
p53
p21?p16?p27?Rb
TNF-?
Amo Type
Article
Publication Title
Acta Medica Okayama
Published Date
1997-12
Volume
volume51
Issue
issue6
Publisher
Okayama University Medical School
Start Page
313
End Page
319
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT