MISMATCH REPAIR GENE DEFECTS IN SPORADIC COLORECTAL CANCERS WITH MICROSATELLITE INSTABILITY

被引:736
|
作者
LIU, B
NICOLAIDES, NC
MARKOWITZ, S
WILLSON, JKV
PARSONS, RE
JEN, J
PAPADOPOLOUS, N
PELTOMAKI, P
DELACHAPELLE, A
HAMILTON, SR
KINZLER, KW
VOGELSTEIN, B
机构
[1] JOHNS HOPKINS ONCOL CTR,BALTIMORE,MD 21231
[2] CASE WESTERN RESERVE UNIV,CLEVELAND,OH 44106
[3] UNIV CLEVELAND HOSP,DEPT MED,CLEVELAND,OH 44106
[4] UNIV CLEVELAND HOSP,IRELAND CANC CTR,CLEVELAND,OH 44106
[5] UNIV HELSINKI,DEPT MED GENET,SF-00290 HELSINKI,FINLAND
[6] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,BALTIMORE,MD 21205
关键词
D O I
10.1038/ng0195-48
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Microsatellite instability has been observed in both sporadic and hereditary forms of colorectal cancer. In the hereditary form, this instability is generally due to germline mutations in mismatch repair (MMR) genes. However, only one in ten patients with sporadic tumours exhibiting microsatellite instability had a detectable germline mutation. Moreover, only three of seven sporadic tumour cell lines with microsatellite instability had mutations in a MMR gene, and these mutations could occur somatically. These results demonstrate that tumours can acquire somatic mutations that presumably do not directly affect cell growth but result only in genetic instability. They also suggest that many sporadic tumours with microsatellite instability have alterations in genes other than the four now known to participate in MMR.
引用
收藏
页码:48 / 55
页数:8
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