Genetic Instability and Mutations of Mismatch Repair (MMR) and p53 Gene in Colorectal Cancers with Multiple Polyps and Sporadic Colorectal Cancers.
- Author:
Sung Won CHUN
1
;
Suk Kyun CHANG
Author Information
1. Department of Surgery, College of Medicine, The Catholic University of Korea, Seoul, Korea. skchang@catholic.ac.kr
- Publication Type:Original Article
- Keywords:
Sporadic colorectal cancer;
Colorectal cancer with multiple polyps;
Genetic instability;
p53 gene
- MeSH:
Adenomatous Polyposis Coli;
Carcinogenesis;
Codon;
Colonic Neoplasms;
Colorectal Neoplasms*;
Colorectal Neoplasms, Hereditary Nonpolyposis;
DNA;
DNA Mismatch Repair*;
Fertilization;
Genes, APC;
Genes, p53*;
Introns;
Point Mutation;
Polymorphism, Single-Stranded Conformational;
Polyps*;
Rectal Neoplasms
- From:Journal of the Korean Society of Coloproctology
2002;18(6):353-362
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: General conceptions of carcinogenic mechanisms by recent reports are ras-p53 gene pathway in sporadic colorectal cancers (SCC), MMR gene pathway in hereditary nonpolyposis colorectal cancer (HNPCC) and APC gene in familial adenomatous polyposis (FAP). But in the colorectal cancer with multiple polyps (CCMP), the carcinogenic pathway is not still defined exactly. In order to find out the which carcinogenic pathway control the CCMP and SCC, genetic instability were studied in CCMP and SCC. METHODS: In this study, genetic instability on D2S123, D3S1029, D5S107, D6S87 and AP delta3 foci and gene mutations of hMLH1 (exon 2, 16, 19), hMSH2 (exon 11, 12, 13, 14) gene of MMR gene, p53 gene (exon 5, 6, 7, 8, 9) were studied on the 60 DNA samples of CCMP (30 cases) and SCC (30 cases). RESULTS: 1. Observed positive genetic instability was higher in CCMP (30%) than SCC (20%), and was higher in right colon cancers (33%) than left colon cancers (23%) or rectal cancers (17%), but not significant statisitically. And observed positive genetic instability was lower in moderate differentiated cancers (16%) than well (67%) or poorly (60%) differentiated cancers (P=0.005). 2. Any mutations of hMLH1 and hMSH2 gene of MMR gene were not observed in both of CCMP and SCC, but 3 cases (2 CCMPs and 1 SCC) point mutations of intron of hMSH2 gene, which were higher in positive genetic instability than negative (P=0.002). 3. This 3 cases point mutations were C for T which were on 6th bases upstream from codon 669. 4. From the results of SSCP for nucleotide sequencing of p53 gene, the abnormal bands were observed in 30% (9 of 30) of CCMP and SCC. Also the abnormal bands were observed in both of positive or negative genetic instability without differences. CONCLUSIONS: With above results the authors suggested that the mechanism of genetic instability and mutations of p53 gene strongly affect the mechanism of carcinogenesis in SCC and CCMP. And there are relationship between genetic instability and point mutation at intron region of hMSH2 gene. However further evaluation and research is needed to establish relation between APC gene and other different kind of MMR gene.
