DNA mismatch repair and cancer

被引:58
作者
Li, GM [1 ]
机构
[1] Univ Kentucky, Med Ctr, Lucille P Markey Canc Ctr, Lexington, KY 40536 USA
[2] Univ Kentucky, Med Ctr, Dept Pathol, Lexington, KY 40536 USA
[3] Univ Kentucky, Med Ctr, Dept Biochem, Lexington, KY 40536 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2003年 / 8卷
关键词
mismatch repair; HNPCC; microsatellite instability; cancer; apoptosis; review;
D O I
10.2741/1121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA mismatch repair (MMR) is an important genome caretaker system. It ensures genomic stability by correcting mismatches generated during DNA replication and recombination and by triggering apoptosis of cells with large amounts of DNA damage. Protein components responsible for these reactions are highly conserved through evolution, and homologs of bacterial MutS and MutL, which are key players in the initiation steps of both the strand-specific mismatch correction and MMR-dependent apoptotic signaling, have been identified in human cells. Inactivation of genes encoding these activities leads to genome-wide instability, particularly in simple repetitive sequences, and predisposition to certain types of cancer, including hereditary non-polyposis colorectal cancer.
引用
收藏
页码:D997 / U1
页数:22
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