Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype

被引:10
作者
de Silva, MG
Kantharidis, P
Scherer, SW
Rayeroux, K
Campbell, L
Tsui, LC
Zalcberg, JR
机构
[1] Peter MacCallum Canc Inst, Div Haematol & Med Oncol, Melbourne, Vic 3000, Australia
[2] Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, Canada
[3] St Vincents Hosp, Dept Cytogenet, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0165-4608(98)00195-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Both the expression of the multidrug transporter, P-glycoprotein (Pgp), and abnormalities of the long arm of chromosome 7 have been shown to be adverse prognostic indicators in acute leukemias. In this study, a clonal duplication, dup(7)(q11.1q31.1), inherited with the classical multidrug resistant phenotype in a drug-resistant derivative of a human T-cell leukemia cell line was characterized. The position of the duplication was of interest as the gene which encodes Pgp, MDR1, is located an the long arm of chromosome 7 at position 7q21.1. Fluorescence in situ hybridization (FISH) analysis with a chromosome 7-specific painting probe confirmed the composition of the abnormal chromosome. A YAC clone hybridizing to the MDR1 locus confirmed that this gene was located within the duplicated region of the derivative chromosome. With a panel of well-characterized YAC clones, the duplicated segment was found to be a direct tandem duplication, somewhat larger than estimated by conventional cytogenetics. The proximal and distal breakpoints of the abnormality were located and a YAC clone spanning the distal breakpoint was identified. This clone is of particular interest, as it harbors the markers D7S523 and D7S471, close to which a putative tumor suppressor gene is thought to lie. Further examination of the breakpoint region may therefore illuminate mechanism of Pgp upregulation as well as providing information about a tumor suppressor gene. (C) Elsevier Science Inc., 1999. All rights reserved.
引用
收藏
页码:28 / 33
页数:6
相关论文
共 33 条
[1]  
Achille A, 1996, CANCER RES, V56, P3808
[2]  
CAMPOS L, 1992, BLOOD, V79, P473
[3]  
DelPoeta G, 1996, BLOOD, V87, P1997
[4]   Inheritance of chromosome 7 is associated with a drug-resistant phenotype in somatic cell hybrids [J].
deSilva, M ;
Kantharidis, P ;
Wall, DM ;
Campbell, L ;
Vrazas, V ;
Nadalin, G ;
Kaczmarczyk, SJ ;
Hu, XF ;
Parkin, JD ;
Zalcberg, JR .
BRITISH JOURNAL OF CANCER, 1996, 73 (02) :169-174
[5]  
FOLEY GE, 1965, CANCER, V18, P522, DOI 10.1002/1097-0142(196504)18:4<522::AID-CNCR2820180418>3.0.CO
[6]  
2-J
[7]   Acquisition of doxorubicin resistance in human leukemia HL-60 cells is reproducibly associated with 7q21 chromosomal anomalies [J].
Ganapathi, R ;
Hoeltge, G ;
Casey, G ;
Grabowski, D ;
Neelon, R ;
Ford, J .
CANCER GENETICS AND CYTOGENETICS, 1996, 86 (02) :116-119
[8]  
GOASGUEN JE, 1993, BLOOD, V81, P2394
[9]   CHARACTERIZATION OF 7Q- BY FISH TECHNIQUE OF A CASE WITH ACUTE MYELOGENOUS LEUKEMIA EVOLVING FROM AGNOGENIC MYELOID METAPLASIA [J].
GOGINENI, SK ;
ELIZAIDE, A ;
SANCHEZ, MA ;
VERMA, RS .
LEUKEMIA RESEARCH, 1995, 19 (07) :481-483
[10]   PREDICTIVE VALUE FOR TREATMENT OUTCOME IN ACUTE MYELOID-LEUKEMIA OF CELLULAR DAUNORUBICIN ACCUMULATION AND P-GLYCOPROTEIN EXPRESSION SIMULTANEOUSLY DETERMINED BY FLOW-CYTOMETRY [J].
GUERCI, A ;
MERLIN, JL ;
MISSOUM, N ;
FELDMANN, L ;
MARCHAL, S ;
WITZ, F ;
ROSE, C ;
GUERCI, O .
BLOOD, 1995, 85 (08) :2147-2153