Coping with complexity:: multivariate analysis of tumor karyotypes

被引:53
作者
Höglund, M [1 ]
Gisselsson, D
Säll, T
Mitelman, F
机构
[1] Univ Lund Hosp, Dept Clin Chem, S-22185 Lund, Sweden
[2] Lund Univ, Dept Genet, S-22362 Lund, Sweden
关键词
D O I
10.1016/S0165-4608(01)00645-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human cancers are characterized by chromosomal aberrations, and an increasing number of specific balanced rearrangements have been found among malignant hematologic disorders. Most solid tumors, however, exhibit a much more complex cytogenetic pattern. Although these chromosome changes show a non-random distribution, tumor-specific aberrations are uncommon, and the solid tumors often contain a large number of abnormalities and also display extensive cytogenetic variability. The high level of karyotypic complexity has made a systematic characterization of the chromosomal patterns difficult. In order to better understand the biological relevance of highly abnormal karyotypes in tumor cell Populations, novel statistical strategies are needed. We have developed and adapted several methods that may be useful for the evaluation of general patterns of karyotypic complexity, including distribution analysis of cytogenetic imbalances, temporal analysis for time of occurrence of aberrations, and principal component analysis for reconstructing karyotypic pathways. By applying these methods on the chromosomal changes presently known, distinct subgroups have been identified among breast, kidney, bladder, colon, and brain tumors. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 13 条
  • [1] Abnormal nuclear shape in solid tumors reflects mitotic instability
    Gisselsson, D
    Björk, J
    Höglund, M
    Mertens, F
    Dal Cin, P
    Åkerman, M
    Mandahl, N
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (01) : 199 - 206
  • [2] Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
    Gisselsson, D
    Pettersson, L
    Höglund, M
    Heidenblad, M
    Gorunova, L
    Wiegant, J
    Mertens, F
    Dal Cin, P
    Mitelman, F
    Mandahl, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) : 5357 - 5362
  • [3] Heim S, 1996, CANCER SURV, V28, P247
  • [4] Heim S., 2015, CANC CYTOGENETICS
  • [5] Höglund M, 2001, GENE CHROMOSOME CANC, V31, P156
  • [6] Höglund M, 2001, CANCER RES, V61, P8241
  • [7] JIN C, 2002, IN PRESS CANC GENET
  • [8] Kachigan S, 1996, STAT ANAL
  • [9] Mertens F, 1997, CANCER RES, V57, P2765
  • [10] A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
    Mitelman, F
    Mertens, F
    Johansson, B
    [J]. NATURE GENETICS, 1997, 15 (Suppl 4) : 417 - 474