Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease

被引:879
作者
Aaltonen, LA
Salovaara, R
Kristo, P
Canzian, F
Hemminki, A
Peltomäki, P
Chadwick, RB
Kääriäinen, H
Eskelinen, M
Järvinen, H
Mecklin, JP
de la Chapelle, A
Percesepe, A
Ahtola, H
Härkönen, N
Julkunen, R
Kangas, E
Ojala, S
Tulikoura, J
ValKamo, E
机构
[1] Univ Helsinki, Haartman Inst, Dept Med Genet, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Haartman Inst, Dept Pathol, FIN-00014 Helsinki, Finland
[3] Perkin Elmer Corp, Appl Biosyst Div, Foster City, CA USA
[4] Ohio State Univ, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA
[5] Family Federat Finland, Helsinki, Finland
[6] Cent Hosp Jyvaskyla, Dept Surg, Jyvaskyla, Finland
[7] Kuopio Univ Hosp, Dept Surg, SF-70210 Kuopio, Finland
[8] Univ Helsinki, Cent Hosp, Dept Surg 2, Helsinki, Finland
[9] Cent Hosp Joensuu, Dept Surg, Joensuu, Finland
[10] Cent Hosp Mikkeli, Dept Surg, Mikkeli, Finland
[11] Kuopio Univ Hosp, Dept Internal Med, SF-70210 Kuopio, Finland
[12] Cent Hosp Lappenranta, Dept Surg, Lappeenranta, Finland
[13] Cent Hosp Kajaani, Dept Surg, Kajaani, Finland
[14] Cent Hosp Kotka, Dept Surg, Kotka, Finland
[15] Cent Hosp Savonlinna, Dept Surg, Savonlinna, Finland
关键词
D O I
10.1056/NEJM199805213382101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Genetic disorders that predispose people to colorectal cancer include the polyposis syndromes and hereditary nonpolyposis colorectal cancer. In contrast to the polyposis syndromes, hereditary nonpolyposis colorectal cancer lacks distinctive clinical features. However, a germ-line mutation of DNA mismatch-repair genes is a characteristic molecular feature of the disease. Since clinical screening of carriers of such mutations can help prevent cancer, it is important to devise strategies applicable to molecular screening for this disease. Methods We prospectively screened tumor specimens obtained from 509 consecutive patients with colorectal adenocarcinomas for DNA replication errors, which are characteristic of hereditary colorectal cancers. These replication errors were detected through microsatellite-marker analyses of tumor DNA. DNA from normal tissue from the patients with replication errors was screened for germ-line mutations of the mismatch-repair genes MLH1 and MSH2. Results Among the 509 patients, 63 (12 percent) had replication errors. Specimens of normal tissue from 10 of these 63 patients had a germ-line mutation of MLH1 or MSH2. Of these 10 patients (2 per cent of the 509 patients), 9 had a first-degree relative with endometrial or colorectal cancer, 7 were under 50 years of age, and 4 had had colorectal or endometrial cancer previously. Conclusions In this series of patients with colorectal-cancer in Finland, at least 2 percent had hereditary nonpolyposis colorectal cancer. We recommend testing for replication errors in all patients with colorectal cancer who meet one or more of the following criteria: a family history of colorectal or endometrial cancer, an age of less than 50 years, and a history of multiple colorectal or endometrial cancers. Patients found to have replication errors should undergo further analysis for germ-line mutations in DNA mismatch-repair genes. (C) 1998, Massachusetts Medical Society.
引用
收藏
页码:1481 / 1487
页数:7
相关论文
共 43 条
  • [1] AALTONEN LA, 1994, CANCER RES, V54, P1645
  • [2] CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER
    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
    [J]. SCIENCE, 1993, 260 (5109) : 812 - 816
  • [3] AALTONEN LA, 1994, CANCER DETECT PREV, V18, P57
  • [4] Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome
    Aarnio, M
    Mecklin, JP
    Aaltonen, LA
    NystromLahti, M
    Jarvinen, HJ
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (06) : 430 - 433
  • [5] AKIYAMA Y, 1957, CANCER RES, V57, P3920
  • [6] Microsatellite instability in early onset and familial colorectal cancer
    Brassett, C
    Joyce, JA
    Froggatt, NJ
    Williams, G
    Furniss, D
    Walsh, S
    Miller, R
    Evans, DGR
    Maher, ER
    [J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (12) : 981 - 985
  • [7] *CANC SOC FINL, 1996, CANC SOC FINL PUBL, V57
  • [8] Canzian F, 1996, CANCER RES, V56, P3331
  • [9] Chadwick RB, 1996, BIOTECHNIQUES, V20, P676
  • [10] Genetics of hereditary colon cancer
    delaChapelle, A
    Peltomaki, P
    [J]. ANNUAL REVIEW OF GENETICS, 1995, 29 : 329 - 348