MICROSATELLITE INSTABILITY IS ASSOCIATED WITH TUMORS THAT CHARACTERIZE THE HEREDITARY NONPOLYPOSIS COLORECTAL-CARCINOMA SYNDROME

被引:2
|
作者
PELTOMAKI, P
LOTHE, RA
AALTONEN, LA
PYLKKANEN, L
NYSTROMLAHTI, M
SERUCA, R
DAVID, L
HOLM, R
RYBERG, D
HAUGEN, A
BROGGER, A
BORRESEN, AL
DELACHAPELLE, A
机构
[1] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT GENET,N-0310 OSLO,NORWAY
[2] NORWEGIAN RADIUM HOSP,INST CANC RES,DEPT PATHOL,N-0310 OSLO,NORWAY
[3] HOSP SAO JOAO,FAC MED,IPATIMUP,GENET UNIT,P-4200 OPORTO,PORTUGAL
[4] NATL INST OCCUPAT HLTH,DEPT TOXICOL,N-0033 OSLO,NORWAY
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microsatellite instability implying multiple replication errors (RER+ phenotype) characterizes a proportion of colorectal carcinomas, particularly those from patients with the hereditary non-polyposis colorectal carcinoma syndrome. We studied the incidence of microsatellite instability in more than 500 sporadic tumors representing 6 different types of cancer. Apart from colorectal carcinoma [see the paper by Lothe et al. (Cancer Res., 53: 5849-5852, 1993)] the RER+ phenotype was found in 18% (6 of 33) of gastric carcinomas and 22% (4 of 18) of endometrial carcinomas. In contrast, no evidence of this abnormality was detected in cancers of the lung (N = 85), breast (N = 84), and testis (N = 86). Importantly, the first three cancers, as opposed to the latter three, are characteristic of the hereditary non-polyposis colorectal carcinoma syndrome. These findings suggest that the cancers belonging to the hereditary non-polyposis colorectal carcinoma tumor spectrum may have essential pathogenetic steps in common, including a tendency to multiple replication errors.
引用
收藏
页码:5853 / 5855
页数:3
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