Does MSI-low exist?

被引:92
作者
Tomlinson, I
Halford, S
Aaltonen, L
Hawkins, N
Ward, R
机构
[1] Imperial Canc Res Fund, Mol & Populat Genet Lab, London WC2A 3PX, England
[2] John Radcliffe Hosp, Inst Mol Med, Imperial Canc Res Fund, Canc Immunogenet Lab, Oxford OX3 9DZ, England
[3] Univ Helsinki, Biomedicum Helsinki, Dept Med Genet, Finnish Canc Inst, FIN-00014 Helsinki, Finland
[4] Univ New S Wales, Sch Pathol, Sydney, NSW 2052, Australia
[5] St Vincents Hosp, Dept Med Oncol, Darlinghurst, NSW 2010, Australia
关键词
microsatellite instability; MSI-low; MSI-L; microsatellite stable; MSS; colorectal cancer;
D O I
10.1002/path.1071
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microsatellite instability is a well-recognised phenomenon. Ten to 15% of sporadic colorectal cancers with a high level of NISI form a well defined group with distinct clinicopathological features. The set of tumours with low level of microsatellite instability (MSI-low), though widely referred to, is not a clearly defined group. The definitions of MSI-low have varied among groups and between different studies from the same group. Some studies have found associations between the NISI-L phenotype and molecular features, notably a higher frequency of K-ras mutations, and, possibly, methylation of methylguanine methyltransferase. Two recent independent studies, however, showed respectively that 68% and 79%, non-MSI-H cancers showed some MSI and could therefore be classed nominally as MSI-L. There was no evidence for a qualitatively discrete NISI-L group, but quantitative differences in the level of NISI were found. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:6 / 13
页数:8
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