P. Hammel et al., Correlations between p53-protein accumulation, serum antibodies and gene mutation in colorectal cancer, INT J CANC, 81(5), 1999, pp. 712-718
Only half of colorectal-cancer patients elicit serum antibodies in response
to intratumoral p53-gene mutations. Our study was designed to compare cell
ular events (p53-protein accumulation and gene mutations) with the presence
of circulating anti-p53 antibodies (p53-Ab). Thirty-five colorectal-cancer
patients were studied for their intratumoral p53-protein accumulation and
circulating p53-Ab. Tumour DNA was analyzed for genomic mutations in a sub-
set of 28 patients. In all, 18 tumours (51.4%) were positive by immunohisto
chemistry, and 17 tumour extracts were shown to contain "mutant" conformati
on p53 protein, 16 of them being were concordant by both methods. Of the 28
tumours tested by DGGE, 16 contained alterations in p53 exons 5 to 8 (57.1
%), Of 12 tumours without detectable mutations, 10 were "mutant"-conformati
on-negative by immunohistochemistry and ELISA. Paradiploid tumors presented
more frequently wild-type p53 genes and were significantly less frequently
immunohistochemistry- or p53-Ab-positive than polyploid tumors. Circulatin
g p53-Ab were detected in the serum of I I patients (31%). In 9/1 I cases,
a gene mutation was found in the corresponding tumour. Three of four mutati
ons in exon 8 and 3/3 mutations in exons 5-6 were associated with p53-Ab, i
n contrast with only 3/9 mutations in exon 7, We found good agreement in th
e detection of p53-gene alterations by different methods. However; our data
suggest that all gene mutations may not be equivalent in term of immunogen
icity. (C) 1999 Wiley-Liss, Inc.