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Detection and evaluation of p53 intron 2 polymorphism in lung carcinomas in Hong Kong

✍ Scribed by Hong Ge; Wah K. Lam; Joseph Lee; Maria P. Wong; Kin H. Fu; Wing W. Yew; Maria L. Lung


Publisher
John Wiley and Sons
Year
1996
Tongue
French
Weight
618 KB
Volume
69
Category
Article
ISSN
0020-7136

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✦ Synopsis


A polymorphism in intron 2 of the p53 gene, which gives rise to 2 alleles, A l and A2, was analyzed by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and direct DNA-sequencing techniques. The distribution of this allele in the peripheral blood in the Chinese population comprising 27 healthy individuals, 30 bronchiectasis patients, 34 non-small-cell lung cancer (NSCLC) patients and 27 SCLC patients was analyzed. The genotypic distributions for this marker were significantly different between the blood of healthy individuals and SCLC patients. There was no significant difference between genotypes of Caucasians and Chinese. Tumors, normal lungs and peripheral blood of 83 adenocarcinoma and I0 squamous cell carcinoma patients were also studied. There was a significant difference in the distribution of the genotypes detected in tumor tissues vf. blood of adenocarcinoma patients. The frequency of detection of the A / / A / genotype in the tumor tissues was increased in adenocarcinoma patients as compared with the blood of adenocarcinoma patients and was decreased in the blood of SCLC patients as compared with the blood of healthy individuals. Survival rates in Hong Kong adenocarcinoma patients with the A / / A / genotype were lower than those in patients with A / /A2 and A2/A2 genotypes up to 30 months post-operation. Point mutations were detected at the p53 intron 2 polymorphic locus in NSCLC specimens, with a mutation rate of 15.4% (8/52). All mutations were GC transversions.

The significance of this instability in p53 intron 2 remains to be elucidated.


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