The tumour samples of 23 patients (9 male, 14 female, aged 25-85) were rand
omly selected for the study. DNA was isolated fi om paraffin embedded tissu
e for quantitative dot-blot hybridization, in order to determine the amplif
ication values for the c-myc and k-ras oncogenes. The clinical and histolog
ical parameters studied were as follows: grade, TNM staging system, Lauren'
s histological type, localization and the severity bf the disease. Amplifie
d c-myc was found in 6 cases. Amplification was concomitant with c-myc over
expression detected with immunohistochemical staining The amplification - 9
.1-fold on the average (ranging from 2.12 to 18.2) was significantly associ
ated with the presence of distant metastasis (corr. coeff: 0.5623, p<0.01),
but with none of the other parameters. No case with K-ras amplification wa
s recorded. The result of the multivariate cluster analysis proved that age
was the decisive factor in the segregation process. This age-related distr
ibution (69 vs. 40, p<0.001), however; did not coincide with either the inc
idence of distant metastasis ol c-myc amplification.