Distinctive patterns of p53 protein expression and microsatellite instability in human colorectal cancer.

Details

Serval ID
serval:BIB_A0CFC1650AD3
Type
Article: article from journal or magazin.
Collection
Publications
Title
Distinctive patterns of p53 protein expression and microsatellite instability in human colorectal cancer.
Journal
Human Pathology
Author(s)
Nyiraneza C., Jouret-Mourin A., Kartheuser A., Camby P., Plomteux O., Detry R., Dahan K., Sempoux C.
ISSN
1532-8392 (Electronic)
ISSN-L
0046-8177
Publication state
Published
Issued date
2011
Peer-reviewed
Oui
Volume
42
Number
12
Pages
1897-1910
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't Publication Status: ppublish
Abstract
Although evidence suggests an inverse relationship between microsatellite instability and p53 alterations in colorectal cancer, no study has thoroughly examined the use of p53 immunohistochemistry in phenotyping colorectal cancers. We investigated the value of p53 immunohistochemistry in microsatellite instability-positive colorectal cancers prescreening and attempted to clarify the relationship between DNA mismatch repair system and p53 pathway. In a series of 104 consecutive colorectal cancers, we performed p53 immunohistochemistry, TP53 mutational analysis, DNA mismatch repair system efficiency evaluation (DNA mismatch repair system immunohistochemistry, microsatellite instability status, MLH1/MSH2 germ line, and BRAF, murine double minute 2, and p21 immunohistochemistry. Microsatellite instability high was observed in 25 of 104 colorectal cancers, with DNA mismatch repair system protein loss (24/25) and germ line (8/25) or BRAF mutations (8/25). p53 immunohistochemistry revealed 3 distinct patterns of expression: complete negative immunostaining associated with truncating TP53 mutations (P < .0001), diffuse overexpression associated with missense TP53 mutations (P < .0001), and restricted overexpression characterized by a limited number of homogenously scattered strongly positive tumor cells in 36.5% of colorectal cancers. This latest pattern was associated with wild-type TP53 and microsatellite instability high colorectal cancers (P < .0001) including all Lynch tumors (8/8), but its presence among 22% of DNA mismatch repair system-competent colorectal cancers decreased its positive predictive value (55.2% [95% confidence interval, 45%-65%]). It was also correlated with murine double minute 2 overexpression (P < .0001) and inversely with p21 loss (P = .0002), independently of microsatellite instability status. In conclusion, a restricted pattern of p53 overexpression is preferentially associated with microsatellite instability high phenotype and could, therefore, be of clinical use as signal for microsatellite instability analysis in a large-scale tumor screening. Its association with concomitant murine double minute 2 overexpression suggests an alternative mechanism of p53 pathway deregulation.
Keywords
Animals, Cohort Studies, Colorectal Neoplasms/genetics, Colorectal Neoplasms/metabolism, Confidence Intervals, Cyclin-Dependent Kinase Inhibitor p21/metabolism, DNA Mismatch Repair, DNA Mutational Analysis, DNA, Neoplasm/genetics, Gene Expression Regulation, Neoplastic, Germ-Line Mutation/genetics, Humans, Mice, Microsatellite Instability, Mutation, Neoplasm Proteins/genetics, Neoplasm Proteins/metabolism, Phenotype, Predictive Value of Tests, Proto-Oncogene Proteins B-raf/metabolism, Proto-Oncogene Proteins c-mdm2/metabolism, Tumor Markers, Biological/genetics, Tumor Markers, Biological/metabolism, Tumor Suppressor Protein p53/genetics, Tumor Suppressor Protein p53/metabolism
Pubmed
Web of science
Create date
19/01/2015 10:50
Last modification date
20/08/2019 15:06
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