Abstract |
The modifications of gene expression by tumor promoters were analyzed in vitro and in vivo. The results of slot blot hybridizations showed that tumor promoter TPA induced c-fos and c-myc expressions in mouse fibroblast cell line BALB/3T3 and rat liver, decreased the levels of Rb RNA in BALB/3T3 cell line and of alpha 1-I3 RNA in rat liver. It was also demonstrated that tumor promoter phenobarbital influenced c-fos and c-myc expressions and decreased alpha 1I3 mRNA level in rat liver during a long term experiment. Phenobarbital was found to have no effect on c-fos and c-myc expressions in rat liver during a short experiment. Tumor promoters induced the expressions of c-fos and c-myc which were positively-related to cancer formation and inhibited the expressions of Rb and alpha 1-I3 which were negatively-related to cancer formation. This implied that tumor promotion played an important role in cancer development and tumor promoters exerted their effects selectively according to the attributes of different genes.
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Authors | C Zhang, Q Zhao, S Guo, M Zhao, S Cheng |
Journal | Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae
(Zhongguo Yi Xue Ke Xue Yuan Xue Bao)
Vol. 17
Issue 1
Pg. 11-5
(Feb 1995)
ISSN: 1000-503X [Print] China |
PMID | 7540119
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Acute-Phase Proteins
- Carcinogens
- Protease Inhibitors
- alpha 1-inhibitor 3
- RNA
- Croton Oil
- Tetradecanoylphorbol Acetate
- Phenobarbital
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Topics |
- 3T3 Cells
(drug effects, metabolism)
- Acute-Phase Proteins
- Animals
- Carcinogens
(toxicity)
- Croton Oil
(pharmacology)
- Gene Expression
(drug effects)
- Genes, Retinoblastoma
- Genes, fos
- Genes, myc
- Liver
(cytology, metabolism)
- Male
- Mice
- Phenobarbital
(pharmacology)
- Protease Inhibitors
(metabolism)
- RNA
(biosynthesis)
- Rats
- Rats, Wistar
- Tetradecanoylphorbol Acetate
(toxicity)
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