Mechanism of Genomic Instability and Its Clinical Applications.
- Author:
Suk Hwan LEE
1
Author Information
1. Department of Surgery, Kyung Hee University College of Medicine, Seoul, Korea. leeshdr@khu.ac.kr
- Publication Type:Review
- Keywords:
Genomic instability;
Microsatellite instability;
Hereditary non-polyposis colorectal cancer;
Epigenetic alteration
- MeSH:
Carcinogenesis;
Colon, Transverse;
Colorectal Neoplasms;
Diagnosis;
DNA Mismatch Repair;
Epigenomics;
Genomic Instability*;
Germ-Line Mutation;
Microsatellite Instability;
Microsatellite Repeats;
Mucins;
Promoter Regions, Genetic
- From:Journal of the Korean Society of Coloproctology
2004;20(1):64-73
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Multiple genetic alterations are common prerequisite for carcinogenesis including colorectal cancers (CRCs). Recently, mutations within microsatellites have been described as a result of defective DNA mismatch repair (MMR) mechanisms, resulting in the phenomenon of microsatellite instability (MSI). This has been implicated in the etiology of hereditary non-polyposis colorectal cancer (HNPCC) and significant portions of sporadic colorectal cancers. However, the mechanisms underlying the MSI are different from hereditary CRCs and sporadic CRCs. While the germline mutation of MMR genes is responsible for HNPCC, the hypermethylation of MLH1 gene promoter regions, an epigenetic, not inherited alteration is responsible for most sporadic CRCs showing MSI. MSI tumors exhibit characteristic clinco- pathologic features, i.e, tumors are preferentially located to proximal to splenic flexure, poorly differentiated, mucinous cell type, frequently showing peritumoral lymphocytic infiltration, and, of importance, showing better survival in stage- matched cases. In this article, the results of recent investigations about MSI and its clinical applications are comprehensively reviewed. Knowledge of these biochemical mechanisms are likely to lead to more effective diagnosis and therapy of CRCs in the future
