The objective of this work was an analysis of mutations in the p53 gen
e detected from fresh tumor samples of larynx cancer patients using si
ngle-strand conformation polymorphism (SSCP) and direct DNA sequencing
of exons 5-8. From 40 patient samples, 15 showed an extra band in SSC
P. In 13 samples mutations were detected in exons 5-8. They constitute
d six transitions and seven transversions, four of them being T to A t
ransversions. Mutations in codons 205 and 248 occurred in two and in c
odon 246 in three samples. Larynx cancer is strongly associated with t
obacco smoking and alcohol consumption. The typical p53 mutations in l
ung cancer, G to T transversions and G to A and C to T transitions, as
sociated with smoking, accounted for 46% of the mutations detected. Fi
fty-four per cent of the mutations were detected in a reported hotspot
region covering codons 238-248.