FAMILIAL ADENOMATOUS POLYPOSIS - MUTATION AT CODON-1309 AND EARLY-ONSET OF COLON-CANCER

被引:181
作者
CASPARI, R
FRIEDL, W
MANDL, M
MOSLEIN, G
KADMON, M
KNAPP, M
JACOBASCH, KH
ECKER, KW
KREISSLERHAAG, D
TIMMERMANS, G
PROPPING, P
机构
[1] UNIV BONN,INST HUMAN GENET,D-53111 BONN,GERMANY
[2] UNIV DUSSELDORF,SURG CLIN,DUSSELDORF,GERMANY
[3] UNIV HEIDELBERG,SURG CLIN,HEIDELBERG,GERMANY
[4] UNIV BONN,INST MED STAT,BONN,GERMANY
[5] UNIV CLIN RUDOLF VIRCHOW,BERLIN,GERMANY
[6] UNIV HOMBURG SAAR,SURG CLIN,HOMBURG,GERMANY
关键词
D O I
10.1016/S0140-6736(94)92634-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical course of familial adenomatous polyposis (FAP) varies considerably between patients. Prediction of the severity of the disease is important in the interest of effective cancer prevention. We examined whether age at diagnosis of FAP due to gastrointestinal symptoms and age at death due to colorectal cancer are related to the site of mutation in the responsible gene. 225 families with FAP were screened for mutations. The deletion of 5 base pairs at codon 1309 within exon 15 (known to be the most common mutation) was identified in 20 families; other mutations within exons 7-15 were found in 49 families. In patients with the 5 base-pair deletion at codon 1309, gastrointestinal symptoms and death from colorectal cancer occurred about 10 years earlier than in patients with other mutations. The 1309 mutation leads to development of colonic polyps at a younger age, thus giving rise to an earlier malignant tranformation. This relationship should be taken into account in strategies for preventing cancer in patients with FAP.
引用
收藏
页码:629 / 632
页数:4
相关论文
共 26 条
  • [1] CASPARI R, 1993, Z GASTROENTEROL, V31, P646
  • [2] MOLECULAR ANALYSIS OF APC MUTATIONS IN FAMILIAL ADENOMATOUS POLYPOSIS AND SPORADIC COLON CARCINOMAS
    COTTRELL, S
    BICKNELL, D
    KAKLAMANIS, L
    BODMER, WF
    [J]. LANCET, 1992, 340 (8820) : 626 - 630
  • [3] 8 NOVEL INACTIVATING GERM LINE MUTATIONS AT THE APC GENE IDENTIFIED BY DENATURING GRADIENT GEL-ELECTROPHORESIS
    FODDE, R
    VANDERLUIJT, R
    WIJNEN, J
    TOPS, C
    VANDERKLIFT, H
    VANLEEUWENCORNELISSE, I
    GRIFFIOEN, G
    VASEN, H
    KHAN, PM
    [J]. GENOMICS, 1992, 13 (04) : 1162 - 1168
  • [4] SINGLE-STEP SCREENING METHOD FOR THE MOST COMMON MUTATIONS IN FAMILIAL ADENOMATOUS POLYPOSIS
    FRIEDL, W
    MANDL, M
    SENGTELLER, M
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (09) : 1481 - 1482
  • [5] IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE
    GRODEN, J
    THLIVERIS, A
    SAMOWITZ, W
    CARLSON, M
    GELBERT, L
    ALBERTSEN, H
    JOSLYN, G
    STEVENS, J
    SPIRIO, L
    ROBERTSON, M
    SARGEANT, L
    KRAPCHO, K
    WOLFF, E
    BURT, R
    HUGHES, JP
    WARRINGTON, J
    MCPHERSON, J
    WASMUTH, J
    LEPASLIER, D
    ABDERRAHIM, H
    COHEN, D
    LEPPERT, M
    WHITE, R
    [J]. CELL, 1991, 66 (03) : 589 - 600
  • [6] GRODEN J, 1993, AM J HUM GENET, V52, P262
  • [7] IDENTIFICATION OF FAP LOCUS GENES FROM CHROMOSOME-5Q21
    KINZLER, KW
    NILBERT, MC
    SU, LK
    VOGELSTEIN, B
    BRYAN, TM
    LEVY, DB
    SMITH, KJ
    PREISINGER, AC
    HEDGE, P
    MCKECHNIE, D
    FINNIEAR, R
    MARKHAM, A
    GROFFEN, J
    BOGUSKI, MS
    ALTSCHUL, SF
    HORII, A
    ANDO, H
    MIYOSHI, Y
    MIKI, Y
    NISHISHO, I
    NAKAMURA, Y
    [J]. SCIENCE, 1991, 253 (5020) : 661 - 665
  • [8] KIRK RE, 1968, EXPT DESIGN PROCEDUR, P299
  • [9] FREQUENCY OF COMMON AND NOVEL INACTIVATING APC MUTATIONS IN 202 FAMILIES WITH FAMILIAL ADENOMATOUS POLYPOSIS
    MANDL, M
    PAFFENHOLZ, R
    FRIEDL, W
    CASPARI, R
    SENGTELLER, M
    PROPPING, P
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (01) : 181 - 184
  • [10] A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS
    MILLER, SA
    DYKES, DD
    POLESKY, HF
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (03) : 1215 - 1215