Y-CHROMOSOME LOSS IN CHRONIC MYELOID-LEUKEMIA DETECTED IN BOTH NORMAL AND MALIGNANT-CELLS BY INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION

被引:25
作者
KIRK, JA
VANDEVANTER, DR
BIBERMAN, J
BRYANT, EM
机构
[1] FRED HUTCHINSON CANC RES CTR,SEATTLE,WA 98104
[2] SWEDISH MED CTR,INST TUMOR,SEATTLE,WA
关键词
D O I
10.1002/gcc.2870110302
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of the Y chromosome in bone marrow (BM) cells is a normal age-associated event. Y chromosome loss is also observed in the Philadelphia chromosome (Ph) positive BM cells of some patients with chronic myeloid leukemia (CML) in chronic phase, but at a younger age than in normal individuals. While the significance of loss of the sex chromosome in normal males is uncertain, -Y marrow cells are not believed to be of clonal origin. However, because CML is a clonal disease, CML sub-populations with Y loss may constitute a disease-related sub-clone. We used a PCR-amplified yeast artificial chromosome containing the BCR gene region for single color interphase analysis of BCR rearrangement by fluorescence in situ hybridization (FISH). Then, using two color FISH, with one fluorochrome detecting the BCR gene region and the other detecting Y chromosome repeat sequences, we surveyed peripheral and BM Y loss in both normal Ph- (BCR not disrupted) and CML Ph+ (BCR rearranged) interphase nuclei of two patients with Y loss in Ph positive cells observed by metaphase analysis. -Y was seen in a proportion of Ph+ cells in both cases, and the proportion matched that seen in Ph- cells, indicating that Y loss is probably sporadic in both normal and CML populations, and that the propensity for Y loss in normal BM cells may be a phenotype that can be retained by malignant cells in CML. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:141 / 145
页数:5
相关论文
共 18 条
[1]   DETECTION OF THE PHILADELPHIA-CHROMOSOME IN INTERPHASE NUCLEI [J].
ARNOLDUS, EPJ ;
WIEGANT, J ;
NOORDERMEER, IA ;
WESSELS, JW ;
BEVERSTOCK, GC ;
GROSVELD, GC ;
VANDERPLOEG, M ;
RAAP, AK .
CYTOGENETICS AND CELL GENETICS, 1990, 54 (3-4) :108-&
[2]   DETECTION OF CHIMERIC BCR-ABL GENES ON BONE-MARROW SAMPLES AND BLOOD SMEARS IN CHRONIC MYELOID AND ACUTE LYMPHOBLASTIC-LEUKEMIA BY IN-SITU HYBRIDIZATION [J].
BENTZ, M ;
CABOT, G ;
MOOS, M ;
SPEICHER, MR ;
GANSER, A ;
LICHTER, P ;
DOHNER, H .
BLOOD, 1994, 83 (07) :1922-1928
[3]   SEQUENCE-INDEPENDENT AMPLIFICATION AND LABELING OF YEAST ARTIFICIAL CHROMOSOMES FOR FLUORESCENCE IN-SITU HYBRIDIZATION [J].
BOHLANDER, SK ;
ESPINOSA, R ;
FERNALD, AA ;
ROWLEY, JD ;
LEBEAU, MM ;
DIAZ, MO .
CYTOGENETICS AND CELL GENETICS, 1994, 65 (1-2) :108-110
[4]   PHILADELPHIA CHROMOSOMAL BREAKPOINTS ARE CLUSTERED WITHIN A LIMITED REGION, BCR, ON CHROMOSOME-22 [J].
GROFFEN, J ;
STEPHENSON, JR ;
HEISTERKAMP, N ;
DEKLEIN, A ;
BARTRAM, CR ;
GROSVELD, G .
CELL, 1984, 36 (01) :93-99
[5]  
LAWLER SD, 1976, SCAND J HAEMATOL, V17, P17
[6]  
LENGAUER C, 1992, CANCER RES, V52, P2590
[7]   CHROMOSOME STUDIES ON BONE MARROW FROM A MALE CONTROL POPULATION [J].
ORIORDAN, ML ;
BERRY, EW ;
TOUGH, IM .
BRITISH JOURNAL OF HAEMATOLOGY, 1970, 19 (01) :83-+
[8]  
PIERRE RV, 1972, CANCER, V30, P889, DOI 10.1002/1097-0142(197210)30:4<889::AID-CNCR2820300405>3.0.CO
[9]  
2-1
[10]  
ROWLEY JD, 1978, SEMIN HEMATOL, V15, P301