A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid malignancies

被引:18
作者
MacKinnon, RN
Campbell, LJ
机构
[1] St Vincent Hosp, Victorian Canc Cytogenet Serv, Fitzroy, Vic 3065, Australia
[2] Univ Melbourne, Dept Med, St Vincent Hosp, Parkville, Vic 3052, Australia
关键词
D O I
10.1016/j.cancergencyto.2005.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We compare two different isochromosomes of chromosome 20 in myelodysplastic syndromes (MDS): an isochromosome of the short arm of chromosome 20, idic(20)(q11), and an isochromosome of the long arm of a deleted chromosome 20, ider(20)(q10)del(20)(q11.2). The isochromosomes are of contrasting morphology, because opposite arms are duplicated, but they both show loss of the critical region at 20q12, as well as retention and duplication of the centromere and proximal long arm (20q11). We speculate that a region of proximal 20q is preferentially retained during deletions of the critical region in MDS and acute myeloid leukemia. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 179
页数:4
相关论文
共 11 条
  • [1] Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes
    Bench, AJ
    Nacheva, EP
    Hood, TL
    Holden, JL
    French, L
    Swanton, S
    Champion, KM
    Li, J
    Whittaker, P
    Stavrides, G
    Hunt, AR
    Huntly, BJP
    Campbell, LJ
    Bentley, DR
    Deloukas, P
    Green, AR
    [J]. ONCOGENE, 2000, 19 (34) : 3902 - 3913
  • [2] CAMPBELL LJ, 1994, LEUKEMIA, V8, P67
  • [3] Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study
    Falzetti, D
    Vermeesch, JR
    Hood, TL
    Nacheva, EP
    Matteucci, C
    Martelli, MF
    Van den Berghe, H
    Marynen, P
    Mecucci, C
    [J]. LEUKEMIA RESEARCH, 1999, 23 (04) : 407 - 413
  • [4] Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in human myeloid malignancies
    Li, J
    Bench, AJ
    Vassiliou, GS
    Fourouclas, N
    Ferguson-Smith, AC
    Green, AR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (19) : 7341 - 7346
  • [5] Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-)
    Li, TY
    Xue, YQ
    Wu, YF
    Pan, JL
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2004, 125 (03) : 337 - 342
  • [6] Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q
    Mrózek, K
    Heinonen, K
    Theil, KS
    Bloomfield, CD
    [J]. GENES CHROMOSOMES & CANCER, 2002, 34 (02) : 137 - 153
  • [7] DOUBLE 20Q - ANOMALY IN MYELODYSPLASTIC SYNDROME
    OHYASHIKI, K
    MURAKAMI, T
    OHYASHIKI, JH
    KODAMA, A
    SAKAI, N
    ITO, H
    TOYAMA, K
    [J]. CANCER GENETICS AND CYTOGENETICS, 1992, 58 (02) : 174 - 176
  • [8] Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes
    Saunders, K
    Czepulkowskia, B
    Sivalingam, R
    Hayes, JPLA
    Aldouri, M
    Sekhar, M
    Cummins, M
    Ho, A
    Mufti, GJ
    [J]. CANCER GENETICS AND CYTOGENETICS, 2005, 156 (02) : 154 - 157
  • [9] Identification of cytogenetic subclasses and recurring chromosomal aberrations in AML and MDS with complex karyotypes using M-FISH
    Van Limbergen, H
    Poppe, B
    Michaux, L
    Herens, C
    Brown, J
    Noens, L
    Berneman, Z
    De Bock, R
    De Paepe, A
    Speleman, F
    [J]. GENES CHROMOSOMES & CANCER, 2002, 33 (01) : 60 - 72
  • [10] Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map
    Wang, PW
    Eisenbart, JD
    Espinosa, R
    Davis, EM
    Larson, RA
    Le Beau, MM
    [J]. GENOMICS, 2000, 67 (01) : 28 - 39