The p53 tumour suppressor gene is inactivated in various types of human can
cers, and has been implicated as an early event in several cancers. A p53 P
ro/Arg polymorphism at exon 4 codon 72, has been suggested to be involved i
n susceptibility to cancers as well. Hence, in the current study, we invest
igated p53 exon 4 codon 72 polymorphism using Proline or Arginine specific
primers from the peripheral blood cells (PBC) representing constitutional D
NA from 72 oral cancer patients. PBC from 153 normal healthy individuals we
re used to determine the frequency of the p53 genotypes, Pro/Pro, Arg/Arg a
nd Pro/Arg, in the Indian population. The frequency of distribution of geno
types in the normal healthy individuals was, Pro/Pro - 0.20 (31/153), Arg/A
rg - 0.14 (22/153) and Pro/Arg - 0.65 (100/153); and in the oral cancer pat
ients was, Pro/Pro - 0.19 (14/72), Arg/Arg - 0.08 (6/72) and Pro/Arg - 0.72
(52/72). Thus, we observed an equidistribution of the genotypes in normal
control and oral cancer patients (chi (2) = 1.77, df = 2, 0.3 < P < 0.5). F
urther, DNA from corresponding tumours from the 72 oral cancer patients wer
e examined for loss of heterozygosity in the p53 gene. Allelic loss was obs
erved in 8 of 52 (15%) heterozygous informative oral cancer patients. Our d
ata indicates an equidistribution of the genotypes and absence of over-repr
esentation of either Pro/Pro or Arg/Arg genotypes in the oral cancer patien
ts as compared to the normal healthy controls. Hence, association of the p5
3 genotypes with susceptibility to oral cancer, was not observed. (C) 2001
Cancer Research Campaign http://www.bjcancer.com.