ATM mutations are rare in familial chronic lymphocytic leukemia

被引:29
作者
Yuille, MR [1 ]
Condie, A [1 ]
Hudson, CD [1 ]
Bradshaw, PS [1 ]
Stone, EM [1 ]
Matutes, E [1 ]
Catovsky, D [1 ]
Houlston, RS [1 ]
机构
[1] Canc Res Inst, Sect Canc Genet, Sutton, Surrey, England
关键词
D O I
10.1182/blood.V100.2.603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It Is now recognized that a subset of B-cell chronic lymphocytic leukemia (CLL) is familial. The genetic basis of familial CLL is poorly understood, but recently germ line mutations in the Ataxia Telanglectasia (ATM) gene have been proposed to confer susceptibility to CLL. The evidence for this notion Is, however, not unequivocal. To examine this proposition further we have screened the ATM gene for mutations in CLLs from 61 individuals in 29 families. Truncating ATM mutations, including a known ATM mutation, were detected in 2 affected individuals, but the mutations did not cosegregate with CLL in the families. In addition, 3 novel ATM missense mutations were detected. Common ATM missense mutations were not overrepresented. The data support previous observations that ATM mutation is associated with B-CLL. However, ATM mutations do not account for familial clustering of the disease. (C) 2002 by The American Society of Hematology.
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收藏
页码:603 / 609
页数:7
相关论文
共 42 条
[1]   The ATM gene and breast cancer:: is it really a risk factor? [J].
Angèle, S ;
Hall, J .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 462 (2-3) :167-178
[2]   Molecular genotyping shows that ataxia-telangiectasia heterozygotes are predisposed to breast cancer [J].
Athma, P ;
Rappaport, R ;
Swift, M .
CANCER GENETICS AND CYTOGENETICS, 1996, 92 (02) :130-134
[3]   Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia [J].
Bevan, S ;
Catovsky, D ;
Marossy, A ;
Matutes, E ;
Popat, S ;
Antonovic, P ;
Bell, A ;
Berrebi, A ;
Gaminara, EJ ;
Quabeck, K ;
Ribeiro, I ;
Mauro, FR ;
Stark, P ;
Sykes, H ;
van Dongen, J ;
Wimperis, J ;
Wright, S ;
Yuille, MR ;
Houlston, RS .
LEUKEMIA, 1999, 13 (10) :1497-1500
[4]  
Bullrich F, 1999, CANCER RES, V59, P24
[5]  
Castellví-Bel S, 1999, HUM MUTAT, V14, P156, DOI 10.1002/(SICI)1098-1004(1999)14:2<156::AID-HUMU7>3.0.CO
[6]  
2-E
[7]   COMPARATIVE HUMAN CELLULAR RADIOSENSITIVITY .2. THE SURVIVAL FOLLOWING GAMMA-IRRADIATION OF UNSTIMULATED (G0) LYMPHOCYTES-T, LYMPHOCYTE-T LINES, LYMPHOBLASTOID CELL-LINES AND FIBROBLASTS FROM NORMAL DONORS, FROM ATAXIA-TELANGIECTASIA PATIENTS AND FROM ATAXIA-TELANGIECTASIA HETEROZYGOTESC [J].
COLE, J ;
ARLETT, CF ;
GREEN, MHL ;
HARCOURT, SA ;
PRIESTLEY, A ;
HENDERSON, L ;
COLE, H ;
JAMES, SE ;
RICHMOND, F .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1988, 54 (06) :929-943
[8]  
CONCANNON P, 2000, ATAXIA TELANGIECTASI
[9]   CANCER RISKS IN A-T HETEROZYGOTES [J].
EASTON, DF .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1994, 66 (06) :S177-S182
[10]  
GALE RP, 1987, SEMIN HEMATOL, V24, P209