CHROMOSOME-ABERRATIONS IN ADENOMAS OF THE COLON - PROOF OF TRISOMY-7 IN TUMOR-CELLS BY COMBINED INTERPHASE CYTOGENETICS AND IMMUNOCYTOCHEMISTRY

被引:28
作者
HERBERGS, J
DEBRUINE, AP
MARX, PTJ
VALLINGA, MIJ
STOCKBRUGGER, RW
RAMAEKERS, FCS
ARENDS, JW
HOPMAN, AHN
机构
[1] UNIV LIMBURG,DEPT MOLEC GENET & CELL BIOL,MAASTRICHT,NETHERLANDS
[2] UNIV LIMBURG HOSP,DEPT INTERNAL MED,MAASTRICHT,NETHERLANDS
关键词
D O I
10.1002/ijc.2910570604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thirty-five colon adenomas from 26 patients were analyzed with centromeric probes for chromosomes 1, 7, 17, X and Y in order to study numerical aberrations, chromosome imbalances, aneuploidy and tetraploidization. The fluorescent in situ hybridization (FISH) technique was applied to single-cell suspensions and a combination of FISH and immunocytochemistry (ICC) was employed to identify the cell type under study. Trisomy of chromosome 7 was detected in 37% of the cases. In 7 out of 13 cases this aberration was combined with abnormalities of one or 2 of the other investigated chromosomes. No correlation could be demonstrated between any of the detected chromosomal aberrations and size, localization or degree of epithelial dysplasia. With the combined FISH/ICC procedure, the abnormal cells were shown to be of epithelial rather than of stromal origin. Our data indicate that trisomy 7 is a common chromosome aberration in the epithelial component of colon adenomas. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:781 / 785
页数:5
相关论文
共 24 条
[1]   INTERPHASE CYTOGENETICS REVEALS SOMATIC PAIRING OF CHROMOSOME-17 CENTROMERES IN NORMAL HUMAN BRAIN-TISSUE, BUT NO TRISOMY-7 OR SEX-CHROMOSOME LOSS [J].
ARNOLDUS, EPJ ;
NOORDERMEER, IA ;
PETERS, ACB ;
RAAP, AK ;
VANDERPLOEG, M .
CYTOGENETICS AND CELL GENETICS, 1991, 56 (3-4) :214-216
[2]  
BARDI G, 1993, CANCER, V71, P306, DOI 10.1002/1097-0142(19930115)71:2<306::AID-CNCR2820710207>3.0.CO
[3]  
2-C
[4]   TRISOMY 7-IN SHORT-TERM CULTURES OF COLORECTAL ADENOCARCINOMAS [J].
BARDI, G ;
JOHANSSON, B ;
PANDIS, N ;
HEIM, S ;
MANDAHL, N ;
ANDRENSANDBERG, A ;
HAGERSTRAND, I ;
MITELMAN, F .
GENES CHROMOSOMES & CANCER, 1991, 3 (02) :149-152
[5]  
CASALONE R, 1992, HUM GENET, V90, P71
[6]   TRISOMY-7 AND TRISOMY-10 CHARACTERIZE SUBPOPULATIONS OF TUMOR-INFILTRATING LYMPHOCYTES IN KIDNEY TUMORS AND IN THE SURROUNDING KIDNEY TISSUE [J].
DALCIN, P ;
ALY, MS ;
DELABIE, J ;
CEUPPENS, JL ;
VANGOOL, S ;
VANDAMME, B ;
BAERT, L ;
VANPOPPEL, H ;
VANDENBERGHE, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (20) :9744-9748
[7]   TRISOMY-7, TRISOMY-10, AND LOSS OF THE Y-CHROMOSOME IN SHORT-TERM CULTURES OF NORMAL KIDNEY TISSUE [J].
ELFVING, P ;
CIGUDOSA, JC ;
LUNDGREN, R ;
LIMON, J ;
MANDAHL, N ;
KRISTOFFERSSON, U ;
HEIM, S ;
MITELMAN, F .
CYTOGENETICS AND CELL GENETICS, 1990, 53 (2-3) :123-125
[8]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767
[9]   DNA FLOW-CYTOMETRY OF ENDOSCOPICALLY EXAMINED COLORECTAL ADENOMAS AND ADENOCARCINOMAS [J].
GIARETTI, W ;
SCIALLERO, S ;
BRUNO, S ;
GEIDO, E ;
ASTE, H ;
DIVINCI, A .
CYTOMETRY, 1988, 9 (03) :238-244
[10]  
GREENBURG G, 1988, DEVELOPMENT, V102, P605