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Amplification of c-erbB-2 oncogene in human adenocarcinomas in vivo
Abstract:
There are two genes related to the viral erbB gene in the human genome. c-erbB-1 is the same as the gene for the epithelial-growth-factor (EGF) receptor, and c-erbB-2 encodes a receptor-like protein very similar to, but distinct from, the EGF receptor. Hybridisation analysis of DNA from 101 fresh human malignant tumours showed that the c-erbB-2 gene was amplified in 5 of 63 adenocarcinomas and none of 38 other types of tumours, whereas the c-erbB-1/EGF-receptor gene was amplified only in 1 of 8 squamous-cell carcinomas. Thus, the protein products of the amplified c-erbB-2 gene may have a role in the evolution of adenocarcinomas, as does the EGF receptor in some squamous-cell carcinomas.
Insights
The c-erbB-2 gene is amplified in some adenocarcinomas, suggesting a role in their development. The epidermal growth factor (EGF) receptor gene (c-erbB-1) is amplified in a small number of squamous-cell carcinomas.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- The human genome contains two genes related to the viral erbB gene: c-erbB-1 (epidermal growth factor receptor) and c-erbB-2.
- c-erbB-2 encodes a receptor-like protein distinct from the EGF receptor.
Purpose of the Study:
- To investigate the amplification of c-erbB-2 and c-erbB-1/EGF-receptor genes in human malignant tumors.
- To determine the potential role of these amplified genes in specific cancer types.
Main Methods:
- DNA hybridization analysis was performed on 101 fresh human malignant tumors.
- Tumors were analyzed for gene amplification of c-erbB-2 and c-erbB-1/EGF-receptor.
Main Results:
- The c-erbB-2 gene was amplified in 5 out of 63 adenocarcinomas.
- No amplification of c-erbB-2 was found in 38 other tumor types.
- The c-erbB-1/EGF-receptor gene was amplified in 1 out of 8 squamous-cell carcinomas.
Conclusions:
- Amplification of the c-erbB-2 gene may play a role in the evolution of adenocarcinomas.
- The EGF receptor gene may be involved in the development of some squamous-cell carcinomas.
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