MICROSATELLITE INSTABILITY IN HUMAN COLONIC-CANCER IS NOT A USEFUL CLINICAL INDICATOR OF FAMILIAL COLORECTAL-CANCER

被引:91
作者
SAMOWITZ, WS [1 ]
SLATTERY, ML [1 ]
KERBER, RA [1 ]
机构
[1] UNIV UTAH,SCH MED,DEPT ONCOL SCI & FAMILY & PREVENT MED,SALT LAKE CITY,UT 84132
关键词
familial standardized incidence ratio; glutathione-S-transferase mu 1; GSTM-1; hereditary nonpolyposis colon cancer; HNPCC; PCR; polymerase chain reaction;
D O I
10.1016/0016-5085(95)90742-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Microsatellite instability is a property of most tumors occurring in the context of hereditary nonpolyposis colon cancer. Instability also occurs in 10%-15% of apparently sporadic colorectal cancers, and it has been hypothesized that this instability may indicate a genetic predisposition to colonic cancer. This study evaluated whether there is a clinically useful association between colon cancer instability and a family history of cancer. Methods: Colon cancer cases (n = 188) from a population-based study were evaluated for microsatellite instability with 10 polymerase chain reaction primer sets. Instability results were compared with family history and other clinical and biological characteristics. Results: Microsatellite instability was found in 16.5% of tumors. It was predominantly a feature of right-sided tumors (P = 0.003) and was associated with the youngest and oldest ages at diagnosis (P = 0.01). Instability was not associated with family history of cancer, sex of the individual, or the glutathione-S-transferase mu 1 null genotype. Conclusions: Although some very small, and as yet undefined, proportion of colon cancer may be caused by inherited mutations leading to microsatellite instability, tumoral instability by itself is not a marker for familiality and should not be considered as evidence for an inherited syndrome.
引用
收藏
页码:1765 / 1771
页数:7
相关论文
共 17 条
[1]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[2]  
BEGG CB, 1994, CANCER EPIDEM BIOMAR, V3, P173
[3]  
Breslow N. E., 1987, STATISTICAL METHODS, VII
[4]   METHOD FOR CALCULATING RISK ASSOCIATED WITH FAMILY HISTORY OF A DISEASE [J].
KERBER, RA .
GENETIC EPIDEMIOLOGY, 1995, 12 (03) :291-301
[5]  
KIM HG, 1994, AM J PATHOL, V145, P148
[6]   SOMATIC MUTATIONS IN THE NEUROFIBROMATOSIS-1 GENE IN HUMAN TUMORS [J].
LI, Y ;
BOLLAG, G ;
CLARK, R ;
STEVENS, J ;
CONROY, L ;
FULTS, D ;
WARD, K ;
FRIEDMAN, E ;
SAMOWITZ, W ;
ROBERTSON, M ;
BRADLEY, P ;
MCCORMICK, F ;
WHITE, R ;
CAWTHON, R .
CELL, 1992, 69 (02) :275-281
[7]   MISMATCH REPAIR GENE DEFECTS IN SPORADIC COLORECTAL CANCERS WITH MICROSATELLITE INSTABILITY [J].
LIU, B ;
NICOLAIDES, NC ;
MARKOWITZ, S ;
WILLSON, JKV ;
PARSONS, RE ;
JEN, J ;
PAPADOPOLOUS, N ;
PELTOMAKI, P ;
DELACHAPELLE, A ;
HAMILTON, SR ;
KINZLER, KW ;
VOGELSTEIN, B .
NATURE GENETICS, 1995, 9 (01) :48-55
[8]  
LOTHE RA, 1993, CANCER RES, V53, P5849
[9]   MUTATIONS OF 2 PMS HOMOLOGS IN HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
NICOLAIDES, NC ;
PAPADOPOULOS, N ;
LIU, B ;
WEI, YF ;
CARTER, KC ;
RUBEN, SM ;
ROSEN, CA ;
HASELTINE, WA ;
FLEISCHMANN, RD ;
FRASER, CM ;
ADAMS, MD ;
VENTER, JC ;
DUNLOP, MG ;
HAMILTON, SR ;
PETERSEN, GM ;
DELACHAPELLE, A ;
VOGELSTEIN, B ;
KINZLER, KW .
NATURE, 1994, 371 (6492) :75-80
[10]   MEDICAL PROGRESS - HEREDITARY GASTROINTESTINAL POLYPOSIS AND NONPOLYPOSIS SYNDROMES [J].
RUSTGI, AK .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (25) :1694-1702