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

Citation
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
Citations number
21
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF CANCER
ISSN journal
00207136 → ACNP
Volume
81
Issue
5
Year of publication
1999
Pages
712 - 718
Database
ISI
SICI code
0020-7136(19990531)81:5<712:CBPASA>2.0.ZU;2-0
Abstract
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.