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Activated c-K-ras and c-N-ras oncogenes in 3-methylcholanthrene-induced BALB/c fibrosarcomas
M G Borrello1, G Carbone, M A Pierotti
1Division of Experimental Oncology A, Istituto Nazionale Tumori, Milan, Italy.
Abstract:
DNAs from fourteen fibrosarcomas induced by 3-methylcholanthrene (MCA) in BALB/c mice were analyzed for the presence of transforming oncogenes following transfection on NIH3T3 cells. Six transfection-positive DNAs contained an activated ras gene: four c-K-ras and two c-N-ras. These results demonstrate that c-K-ras is not the only oncogene of the ras family activated in MCA-induced murine fibrosarcomas as was previously indicated.
Insights
Activated ras oncogenes were identified in mouse fibrosarcomas. Both c-K-ras and c-N-ras were found, indicating ras family diversity in cancer development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- 3-methylcholanthrene (MCA) is a chemical carcinogen known to induce fibrosarcomas in mice.
- Oncogenes, particularly those in the ras family, play critical roles in cancer development.
- Previous studies suggested c-K-ras as the primary activated oncogene in MCA-induced murine fibrosarcomas.
Purpose of the Study:
- To investigate the presence and types of activated oncogenes in fibrosarcomas induced by MCA in BALB/c mice.
- To determine if other members of the ras oncogene family are activated in these tumors.
Main Methods:
- DNA was extracted from fourteen MCA-induced fibrosarcomas in BALB/c mice.
- NIH3T3 cells were transfected with the extracted DNA.
- Transfection-positive DNAs were analyzed for activated ras oncogenes (c-K-ras and c-N-ras).
Main Results:
- Six out of fourteen fibrosarcoma DNA samples contained activated ras oncogenes.
- Four samples showed activation of c-K-ras.
- Two samples demonstrated activation of c-N-ras.
Conclusions:
- The ras oncogene family, specifically c-K-ras and c-N-ras, is activated in MCA-induced murine fibrosarcomas.
- c-K-ras is not the sole activated oncogene within the ras family in these tumors.
- These findings expand the understanding of oncogene activation in chemically induced carcinogenesis.