GENETIC INSTABILITY OCCURS IN THE MAJORITY OF YOUNG-PATIENTS WITH COLORECTAL-CANCER

被引:318
作者
LIU, B
FARRINGTON, SM
PETERSEN, GM
HAMILTON, SR
PARSONS, R
PAPADOPOULOS, N
FUJIWARA, T
JEN, J
KINZLER, KW
WYLLIE, AH
VOGELSTEN, B
DUNLOP, MG
机构
[1] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
[2] JOHNS HOPKINS UNIV,SCH HYG & PUBL HLTH,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,DEPT PATHOL,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,DEPT ONCOL,BALTIMORE,MD 21205
[5] UNIV EDINBURGH,SCH MED,DEPT PATHOL,CANC RES CAMPAIGN LABS,EDINBURGH EH8 9AG,MIDLOTHIAN,SCOTLAND
[6] UNIV EDINBURGH,ROYAL INFIRM,DEPT SURG,EDINBURGH EH3 9YW,MIDLOTHIAN,SCOTLAND
关键词
D O I
10.1038/nm0495-348
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
Replication errors (RER) associated with genetic instability have been found in cancers of several different types and particularly in the tumours of patients with hereditary non-polyposis colorectal cancer (HNPCC). We have here determined the prevalence of such instability in relation to age among patients without HNPCC. Colorectal cancers (CRCs) in the majority of patients 35 years of age or younger exhibited instability (58% of 31 patients), whereas CRCs from patients older than 35 uncommonly did (12% of 158, P < 0.0001). Twelve of the patients under 35 with instability were evaluated for alterations of mismatch repair genes, and five were found to harbour germline mutations. These data suggest that the mechanisms underlying tumour development in young CRC patients differ from those in most order patients, regardless of HNPCC status. The results have important implications for genetic testing and management of young CRC patients and their families.
引用
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页码:348 / 352
页数:5
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