Molecular cytogenetic analysis of breast cancer cell lines

被引:87
作者
Davidson, JM
Gorringe, KL
Chin, SF
Orsetti, B
Besret, C
Courtay-Cahen, C
Roberts, I
Theillet, C
Caldas, C
Edwards, PAW
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] Univ Cambridge, Addenbrookes Hosp, CIMR, Dept Oncol,Wellcome Trust, Cambridge CB2 2XY, England
[3] Ctr Rech Cancerol, UMR CNRS 5535, Equipe Genome & Canc, F-34298 Montpellier, France
基金
英国生物技术与生命科学研究理事会; 澳大利亚研究理事会;
关键词
chromosome translocations; karyotypes; fluorescence-in situ hybridization; spectral karyotyping; comparative genomic hybridization;
D O I
10.1054/bjoc.2000.1458
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The extensive chromosome rearrangements of breast carcinomas must contribute to tumour development, but have been largely intractable to classical cytogenetic banding. We report here the analysis by 24-colour karyotyping and comparative genomic hybridization (CGH) of 19 breast carcinoma cell lines and one normal breast epithelial cell line, which provide model examples of karyotype patterns and translocations present in breast carcinomas. The CGH was compared with CGH of 106 primary breast cancers. The lines varied from perfectly diploid to highly aneuploid. Translocations were very varied and over 98% were unbalanced. The most frequent in the carcinomas were 8;11 in five lines; and 8;17, 1;4 and 1;10 in four lines. The most frequently involved chromosome was 8. Several lines showed complex multiply-translocated chromosomes. The very aneuploid karyotypes appeared to fall into two groups that evolved by different routes: one that steadily lost chromosomes and at one point doubled their entire karyotype; and another that steadily gained chromosomes, together with abnormalities. All karyotypes fell within the range seen in fresh material and CGH confirmed that the lines were broadly representative of fresh tumours. The karyotypes provide a resource for the cataloguing and analysis of translocations in these tumours, accessible at http://www.path.cam.ac.uk/-pawefish. (C) 2000 Cancer Research Campaign.
引用
收藏
页码:1309 / 1317
页数:9
相关论文
共 39 条
  • [1] Adeyinka A, 2000, INT J MOL MED, V5, P235
  • [2] Bautista S, 1998, GENE CHROMOSOME CANC, V22, P268, DOI 10.1002/(SICI)1098-2264(199808)22:4<268::AID-GCC2>3.3.CO
  • [3] 2-U
  • [4] Bernardino L, 1998, GENE CHROMOSOME CANC, V23, P100, DOI 10.1002/(SICI)1098-2264(199810)23:2<100::AID-GCC2>3.0.CO
  • [5] 2-6
  • [6] Courjal F, 1997, CANCER RES, V57, P4368
  • [7] Chromosome translocations in breast cancer with breakpoints at 8p12
    Courtay-Cahen, C
    Morris, JS
    Edwards, PAW
    [J]. GENOMICS, 2000, 66 (01) : 15 - 25
  • [8] BREAST-CANCER GENETIC EVOLUTION .1. DATA FROM CYTOGENETICS AND DNA CONTENT
    DUTRILLAUX, B
    GERBAULTSEUREAU, M
    REMVIKOS, Y
    ZAFRANI, B
    PRIEUR, M
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 1991, 19 (03) : 245 - 255
  • [9] Pathways of chromosome alteration in human epithelial cancers
    Dutrillaux, B
    [J]. ADVANCES IN CANCER RESEARCH, VOL 67, 1995, 67 : 59 - 82
  • [10] Fogh J., 1975, HUMAN TUMOR CELLS IN, P115, DOI DOI 10.1007/978-1-4757-1647-4_5