Breast cancer risk in ataxia telangiectasia (AT) heterozygotes:: haplotype study in French AT families

被引:87
作者
Janin, N
Andrieu, N
Ossian, K
Laugé, A
Croquette, MF
Griscelli, C
Debré, M
Bressac-de-Paillerets, B
Aurias, A
Stoppa-Lyonnet, D
机构
[1] Inst Gustave Roussy, F-94805 Villejuif, France
[2] Inst Gustave Roussy, INSERM, U351, F-94805 Villejuif, France
[3] Inst Curie, Unite Genet Oncol, Lab Pathol Mol Canc, F-75231 Paris, France
[4] Ctr Hosp Feron Vrau, F-59019 Lille, France
[5] Hop Necker Enfants Malad, Serv Immunohematol Pediat, F-75743 Paris 15, France
关键词
ataxia telangiectasia heterozygosis; breast cancer risk; family study;
D O I
10.1038/sj.bjc.6690460
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidemiological studies in ataxia telangiectasia (AT) families have suggested that AT heterozygotes could have an increased cancer risk, especially breast cancer (BC) in women. It has also been suggested that an increased sensibility of AT heterozygotes to the effect of ionizing radiation could be responsible for the increased BC risk. BC relative risk (RR) estimation in AT heterozygotes within families ascertained through AT children is presented here. Family data collected included demographic characteristics, occurrence of cancers, past radiation exposures and blood samples, DNA samples were studied using seven ATM linked microsatellites markers allowing AT haplotypes reconstitution. The relative risk of BC was assessed using French estimated incidence rates. A significant increase risk of BC is found among obligate ATM heterozygotes with a point estimate of 3.32 (P = 0.002). BC relative risk calculated according to age is significantly increased among the obligate ATM heterozygotes female relatives with an age less than or equal to 44 years (RR = 4.55, P = 0.005). The BC relative risk is statistically borderline among the obligate ATM heterozygote female relatives with an age greater than or equal to 45 years (RR = 2.48, P= 0.08), The estimated BC relative risk among ATM heterozygotes is consistent with previously published data. However, the increased risk is only a little higher than classical reproductive risk factors and similar to the risk associated with a first-degree relative affected by BC.
引用
收藏
页码:1042 / 1045
页数:4
相关论文
共 24 条
[1]   HOW ACCURATE IS SELF-REPORTED FAMILY HISTORY OF COLORECTAL-CANCER [J].
AITKEN, J ;
BAIN, C ;
WARD, M ;
SISKIND, V ;
MACLENNAN, R .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1995, 141 (09) :863-871
[2]   Absence of mutations in the ATM gene in breast cancer patients with severe responses to radiotherapy [J].
Appleby, JM ;
Barber, JBP ;
Levine, E ;
Varley, JM ;
Taylor, AMR ;
Stankovic, T ;
Heighway, J ;
Warren, C ;
Scott, D .
BRITISH JOURNAL OF CANCER, 1997, 76 (12) :1546-1549
[3]   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
[4]   ''AT risk'' for breast cancer [J].
Bebb, G ;
Glickman, B ;
Gelmon, K ;
Gatti, R .
LANCET, 1997, 349 (9068) :1784-1785
[5]  
BENHAMOU E, 1990, STAT SANTE
[6]   AT-tributable risks? [J].
Bishop, DT ;
Hopper, J .
NATURE GENETICS, 1997, 15 (03) :226-226
[7]   BREAST-CANCER AND OTHER CANCERS IN NORWEGIAN FAMILIES WITH ATAXIA-TELANGIECTASIA [J].
BORRESEN, AL ;
ANDERSEN, TI ;
TRETLI, S ;
HEIBERG, A ;
MOLLER, P .
GENES CHROMOSOMES & CANCER, 1990, 2 (04) :339-340
[8]  
Breslow NE, 1987, STAT METHODS CANC RE, VII
[9]   COHORT STUDY ANALYSIS WITH A FORTRAN COMPUTER-PROGRAM [J].
COLEMAN, M ;
DOUGLAS, A ;
HERMON, C ;
PETO, J .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1986, 15 (01) :134-137
[10]  
DEVATHAIRC F, 1996, STAT SANTE