Microsatellite instability in early onset and familial colorectal cancer

被引:38
作者
Brassett, C
Joyce, JA
Froggatt, NJ
Williams, G
Furniss, D
Walsh, S
Miller, R
Evans, DGR
Maher, ER
机构
[1] UNIV CAMBRIDGE,DEPT PATHOL,CAMBRIDGE CB1 4QP,ENGLAND
[2] ADDENBROOKES NHS TRUST,DEPT SURG,CAMBRIDGE CB2 2QQ,ENGLAND
[3] TRAFFORD GEN HOSP,MANCHESTER,LANCS,ENGLAND
[4] ST MARYS HOSP,DEPT MED GENET,MANCHESTER M13 0JH,LANCS,ENGLAND
关键词
microsatellite instability; familial colorectal cancer;
D O I
10.1136/jmg.33.12.981
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Hereditary non-polyposis colorectal cancer syndrome (HNPCC) is often considered to be the most common form of inherited colorectal cancer, although its precise incidence is unknown. The clinical diagnosis of HNPCC relies on a combination of family history and young age of onset of colorectal cancer, but as many familial aggregations of colorectal cancer do not fulfil the strict diagnostic criteria, HNPCC might be underdiagnosed. The majority of HNPCC families have germline mutations in mismatch repair (MMR) genes, such as MSH2 or MLH1, so that HNPCC cancers characteristically exhibit DNA replication errors (RERs) at microsatellite loci. Although an RER positive phenotype in tumours can also result from somatic mutations in an MMR gene, the prevalence of RER+ tumours should provide a maximum estimate of the incidence of germline MMR gene mutations in patients with early onset and familial colorectal cancer. We investigated colorectal cancers for RERs from (1) a population based study of 33 patients with colorectal cancer aged 45 years or less, (2) 65 kindreds with familial colorectal cancer which only partially fulfilled the criteria for the diagnosis of HNPCC, and (3) 18 cancers from 12 HNPCC kindreds. Seven of 33 patients (21%) with colorectal cancer aged 45 years or less had an RER+ cancer, with only two of these having a clear family history of HNPCC. A greater proportion of RER+ tumours (5/7) occurred proximal to the splenic flexure than RER- tumours (4/26; chi(2) = 6.14, p < 0.025). RERs were detected in all 18 cancers from HNPCC patients but in only six of 65 non-HNPCC familial colorectal cancer kindreds (9%; chi(2) = 52.2, p < 0.0005). These findings suggest that most cancers in patients diagnosed at 45 years of age or less and familial aggregations of colorectal cancer which do not fulfil HNPCC diagnostic criteria do not have germline mutations in MSH2 and MLH1. Hence population screening for germline mutations in these genes is unlikely to be an efficient strategy for identifying people at high risk of developing colorectal cancer.
引用
收藏
页码:981 / 985
页数:5
相关论文
共 29 条
[1]
AALTONEN LA, 1994, CANCER RES, V54, P1645
[2]
GENETIC-MAPPING OF 12 MARKER LOCI IN THE XP22.3-P21.2 REGION [J].
ALITALO, T ;
KRUSE, TA ;
AHRENS, P ;
ALBERTSEN, HM ;
ERIKSSON, AW ;
DELACHAPELLE, A .
HUMAN GENETICS, 1991, 86 (06) :599-603
[3]
MUTATION IN THE DNA MISMATCH REPAIR GENE HOMOLOG HMLH1 IS ASSOCIATED WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
BRONNER, CE ;
BAKER, SM ;
MORRISON, PT ;
WARREN, G ;
SMITH, LG ;
LESCOE, MK ;
KANE, M ;
EARABINO, C ;
LIPFORD, J ;
LINDBLOM, A ;
TANNERGARD, P ;
BOLLAG, RJ ;
GODWIN, AR ;
WARD, DC ;
NORDENSKJOLD, M ;
FISHEL, R ;
KOLODNER, R ;
LISKAY, RM .
NATURE, 1994, 368 (6468) :258-261
[4]
DETECTION OF NEW MUTATIONS IN 6 OUT OF 10 SWISS HNPCC FAMILIES BY GENOMIC SEQUENCING OF THE HMSH2 AND HMLH1 GENES [J].
BUERSTEDDE, JM ;
ALDAY, P ;
TORHORST, J ;
WEBER, W ;
MULLER, H ;
SCOTT, R .
JOURNAL OF MEDICAL GENETICS, 1995, 32 (11) :909-912
[5]
COMMON INHERITANCE OF SUSCEPTIBILITY TO COLONIC ADENOMATOUS POLYPS AND ASSOCIATED COLORECTAL CANCERS [J].
CANNONALBRIGHT, LA ;
SKOLNICK, MH ;
BISHOP, T ;
LEE, RG ;
BURT, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (09) :533-537
[6]
ISOLATION OF AN HMSH2-P160 HETERODIMER THAT RESTORES DNA MISMATCH REPAIR TO TUMOR-CELLS [J].
DRUMMOND, JT ;
LI, GM ;
LONGLEY, MJ ;
MODRICH, P .
SCIENCE, 1995, 268 (5219) :1909-1912
[7]
THE HUMAN MUTATOR GENE HOMOLOG MSH2 AND ITS ASSOCIATION WITH HEREDITARY NONPOLYPOSIS COLON-CANCER [J].
FISHEL, R ;
LESCOE, MK ;
RAO, MRS ;
COPELAND, NG ;
JENKINS, NA ;
GARBER, J ;
KANE, M ;
KOLODNER, R .
CELL, 1993, 75 (05) :1027-1038
[8]
Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome [J].
Froggatt, NJ ;
Brassett, C ;
Koch, DJ ;
Evans, DGR ;
Hodgson, SV ;
Ponder, BAJ ;
Maher, ER .
JOURNAL OF MEDICAL GENETICS, 1996, 33 (09) :726-730
[9]
A FREQUENT HMSH2 MUTATION IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME [J].
FROGGATT, NJ ;
JOYCE, JA ;
DAVIES, R ;
EVANS, DGR ;
PONDER, BAJ ;
BARTON, DE ;
MAHER, ER .
LANCET, 1995, 345 (8951) :727-727
[10]
GENETIC-LINKAGE ANALYSIS IN HEREDITARY NONPOLYPOSIS COLON-CANCER SYNDROME [J].
FROGGATT, NJ ;
KOCH, J ;
DAVIES, R ;
EVANS, DGR ;
CLAMP, A ;
QUARRELL, OWJ ;
WEISSENBACH, J ;
HODGSON, SV ;
PONDER, BAJ ;
BARTON, DE ;
MAHER, ER .
JOURNAL OF MEDICAL GENETICS, 1995, 32 (05) :352-357