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Genetic predisposition to human lung cancer
British Journal of Cancer
|April 1, 1986
Summary
Genetic variations in the human c-Ha-ras gene may influence lung cancer risk. Specific allele distributions suggest a predisposition to non-small cell lung cancer.
Area of Science:
- Genetics
- Oncology
Background:
- The human c-Ha-ras gene is implicated in cell growth and cancer development.
- Polymorphisms in the c-Ha-ras gene, specifically a BamH1 restriction fragment length polymorphism (RFLP), have been identified.
Purpose of the Study:
- To investigate the association between c-Ha-ras gene polymorphic variants and lung cancer predisposition.
- To compare c-Ha-ras RFLP allele frequencies in normal individuals versus lung cancer patients.
Main Methods:
- DNA was extracted from white blood cells of 101 healthy donors and 132 lung cancer patients (66 small cell lung carcinoma [SCCL], 66 non-small cell lung carcinoma [non-SCCL]).
- c-Ha-ras RFLP allele frequencies were analyzed using DNA extracted from peripheral blood.
- Analysis of solid tumor samples was performed to detect chromosomal abnormalities.
Main Results:
- Four common c-Ha-ras alleles and rare variants were identified in the normal population.
- An abnormal allele distribution of c-Ha-ras RFLP was observed in non-SCCL patients compared to controls and SCCL patients.
- Two of 16 informative samples showed evidence of material deletion from the short arm of chromosome 11.
Conclusions:
- The study suggests a potential genetic predisposition to non-small cell lung cancer linked to c-Ha-ras gene polymorphisms.
- Alterations in the c-Ha-ras locus, including deletions, may play a role in lung cancer development.