Correlations between p53-protein accumulation, serum antibodies and gene mutation in colorectal cancer

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Abstract
Only half of colorectal‐cancer patients elicit serum antibodies in response to intratumoral p53‐gene mutations. Our study was designed to compare cellular 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 immunohistochemistry, and 17 tumour extracts were shown to contain “mutant” conformation 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”‐conformation‐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. Circulating p53‐Ab were detected in the serum of 11 patients (31%). In 9/11 cases, a gene mutation was found in the corresponding tumour. Three of four mutations in exon 8 and 3/3 mutations in exons 5‐6 were associated with p53‐Ab, in contrast with only 3/9 mutations in exon 7. We found good agreement in the detection of p53‐gene alterations by different methods. However, our data suggest that all gene mutations may not be equivalent in term of immunogenicity. Int. J. Cancer 81:712–718, 1999.