APPLICATION OF FLUORESCENCE IN-SITU HYBRIDIZATION TO CHROMOSOME ANALYSIS OF AGED BONE-MARROW SMEARS

被引:9
作者
HAMMOND, DW
HINCHLIFFE, RF
GOYNS, MH
POTTER, AM
LILLEYMAN, JS
机构
[1] UNIV SHEFFIELD,SCH MED,INST CANC STUDIES,SHEFFIELD S10 2UL,S YORKSHIRE,ENGLAND
[2] UNIV SHEFFIELD,SCH MED,DEPT CLIN ONCOL,SHEFFIELD S10 2UL,S YORKSHIRE,ENGLAND
[3] UNIV SHEFFIELD,CHILDRENS HOSP,DEPT PAEDIAT,PAEDIAT HAEMATOL SECT,SHEFFIELD S10 2TH,S YORKSHIRE,ENGLAND
[4] CTR HUMAN GENET,SHEFFIELD,S YORKSHIRE,ENGLAND
关键词
D O I
10.1136/jcp.47.6.508
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims-To evaluate the reliability of fluorescence in situ hybridisation (FISH) in the retrospective cytogenetic assessment of old bone marrow smears stored for periods of up to 20 years. Methods-A series of bone marrow smears either Romanowsky stained, or frozen and unstained, and aged from one month to 20 years were hybridised with biotin labelled probes specific for the centromeric regions of human chromosomes X, 6, and 18. Sites of hybridisation were detected with fluoresceinated avidin. One hundred to 400 cells from each preparation were examined and the number of signals observed was recorded. Results-All smears exhibited signals in most cells examined. In cytogenetically normal cases, an average 67.6% of cells (range 36%-90%) demonstrated the appropriate number of X centromere signals. In those samples known to contain extra chromosomes X, 6, or 18 the presence of cells with the abnormal copy number was clearly detected in each case. Conclusion-When applied in the way described, FISH can give consistent and accurate results with a variety of archival bone marrow smears, including aged prestained material. This will permit retrospective assessment of specific cytogenetic abnormalities in patients with leukaemia using their initial diagnostic slides even where these are several years old.
引用
收藏
页码:508 / 511
页数:4
相关论文
共 15 条
  • [1] ANASTASI J, 1992, BLOOD, V79, P1796
  • [2] ANASTASI J, 1991, BLOOD, V77, P2456
  • [3] DETECTION OF THE PHILADELPHIA-CHROMOSOME IN INTERPHASE NUCLEI
    ARNOLDUS, EPJ
    WIEGANT, J
    NOORDERMEER, IA
    WESSELS, JW
    BEVERSTOCK, GC
    GROSVELD, GC
    VANDERPLOEG, M
    RAAP, AK
    [J]. CYTOGENETICS AND CELL GENETICS, 1990, 54 (3-4): : 108 - &
  • [4] INTERPHASE CYTOGENETICS OF BRAIN-TUMORS
    ARNOLDUS, EPJ
    NOORDERMEER, IA
    PETERS, ACB
    VOORMOLEN, JHC
    BOTS, GTAM
    RAAP, AK
    VANDERPLOEG, M
    [J]. GENES CHROMOSOMES & CANCER, 1991, 3 (02) : 101 - 107
  • [5] ANALYSIS OF PROSTATIC TUMOR CULTURES USING FLUORESCENCE INSITU HYBRIDIZATION (FISH)
    BROTHMAN, AR
    PATEL, AM
    PEEHL, DM
    SCHELLHAMMER, PF
    [J]. CANCER GENETICS AND CYTOGENETICS, 1992, 62 (02) : 180 - 185
  • [6] DETECTION OF CHROMOSOME-ABERRATIONS IN THE HUMAN INTERPHASE NUCLEUS BY VISUALIZATION OF SPECIFIC TARGET DNAS WITH RADIOACTIVE AND NONRADIOACTIVE INSITU HYBRIDIZATION TECHNIQUES - DIAGNOSIS OF TRISOMY-18 WITH PROBE L1.84
    CREMER, T
    LANDEGENT, J
    BRUCKNER, A
    SCHOLL, HP
    SCHARDIN, M
    HAGER, HD
    DEVILEE, P
    PEARSON, P
    VANDERPLOEG, M
    [J]. HUMAN GENETICS, 1986, 74 (04) : 346 - 352
  • [7] HEEREMA NA, 1993, LEUKEMIA, V7, P537
  • [8] DETECTION OF TRISOMY-8 IN HEMATOLOGICAL DISORDERS BY INSITU HYBRIDIZATION
    KIBBELAAR, RE
    VANKAMP, H
    DREEF, EJ
    WESSELS, JW
    BEVERSTOCK, GC
    RAAP, AK
    FIBBE, WE
    DENOTTOLANDER, GJ
    KLUIN, PM
    [J]. CYTOGENETICS AND CELL GENETICS, 1991, 56 (3-4): : 132 - &
  • [9] KIECHLESCHLWARZ M, 1991, CANCER GENET CYTOGEN, V21, P23
  • [10] USE OF FLUORESCENCE IN-SITU HYBRIDIZATION FOR RETROSPECTIVE DETECTION OF ANEUPLOIDY IN MULTIPLE-MYELOMA
    LEE, WB
    HAN, KJ
    DRUT, RM
    HARRIS, CP
    MEISNER, LF
    [J]. GENES CHROMOSOMES & CANCER, 1993, 7 (03) : 137 - 143