J Korean Soc Coloproctol.  2004 Feb;20(1):64-73.

Mechanism of Genomic Instability and Its Clinical Applications

• Lee SH

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

Keyword

Genomic instability; Microsatellite instability; Hereditary non-polyposis colorectal cancer; Epigenetic alteration

MeSH Terms

Carcinogenesis
Colon, Transverse
Colorectal Neoplasms
Diagnosis
DNA Mismatch Repair
Epigenomics
Genomic Instability*
Germ-Line Mutation
Microsatellite Instability
Microsatellite Repeats
Mucins
Promoter Regions, Genetic
Mucins