Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia

被引:80
作者
Inskip, HM [1 ]
Kinlen, LJ
Taylor, AMR
Woods, CG
Arlett, CF
机构
[1] Univ Southampton, Southampton Gen Hosp, MRC, Environm Epidemiol Unit, Southampton SO16 6YD, Hants, England
[2] Univ Oxford, Radcliffe Infirm, CRC, Canc Epidemiol Res Grp, Oxford OX2 6HE, England
[3] Univ Birmingham, CRC, Inst Canc Studies, Birmingham B15 2TA, W Midlands, England
[4] St James Univ Hosp, Yorkshire Reg Genet Serv, Leeds LS9 7TF, W Yorkshire, England
[5] Univ Sussex, MRC, Cell Mutat Unit, Brighton BN1 9RR, E Sussex, England
关键词
ataxia-telangiectasia; breast cancer; cancer mortality;
D O I
10.1038/sj.bjc.6690209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mortality from cancer among 178 parents and 236 grandparents of 95 British patients with ataxia-telangiectasia was examined. For neither parents nor grandparents was mortality from all causes or from cancer appreciably elevated over that of the national population. Among mothers, three deaths from breast cancer gave rise to a standardized mortality ratio of 3.37 (95% confidence interval (CI): 0.69-9.84). In contrast, there was no excess of breast cancer in grandmothers, the standardized mortality ratio being 0.89 (95% CI: 0.18-2.59), based on three deaths. This is the largest study of families of ataxia-telangiectasia patients conducted in Britain but, nonetheless, the study is small and Cis are wide. However, taken together with data from other countries, an increased risk of breast cancer among female heterozygotes is still apparent, though lower than previously thought.
引用
收藏
页码:1304 / 1307
页数:4
相关论文
共 50 条
  • [31] Bronchiolitis obliterans in ataxia-telangiectasia
    Ito, M
    Nakagawa, A
    Hirabayashi, N
    Asai, J
    VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 1997, 430 (02): : 131 - 137
  • [32] Ataxia-telangiectasia, an evolving phenotype
    Chun, HH
    Gatti, RA
    DNA REPAIR, 2004, 3 (8-9) : 1187 - 1196
  • [33] ATM protein and p53-serine 15 phosphorylation in ataxia-telangiectasia (AT) patients and at heterozygotes
    Delia, D
    Mizutani, S
    Panigone, S
    Tagliabue, E
    Fontanella, E
    Asada, M
    Yamada, T
    Taya, Y
    Prudente, S
    Saviozzi, S
    Frati, L
    Pierotti, MA
    Chessa, L
    BRITISH JOURNAL OF CANCER, 2000, 82 (12) : 1938 - 1945
  • [34] Molecular Defects in Moroccan Patients with Ataxia-Telangiectasia
    Jeddane, L.
    Ailal, F.
    Dubois-d'Enghien, C.
    Abidi, O.
    Benhsaien, I.
    Kili, A.
    Chaouki, S.
    Kriouile, Y.
    El Hafidi, N.
    Fadil, H.
    Abilkassem, R.
    Rada, N.
    Bousfiha, A. A.
    Barakat, A.
    Stoppa-Lyonnet, D.
    Bellaoui, H.
    NEUROMOLECULAR MEDICINE, 2013, 15 (02) : 288 - 294
  • [35] More than ataxia - Movement disorders in ataxia-telangiectasia
    Ghizoni Teive, Helio Afonso
    Ferreira Camargo, Carlos Henrique
    Munhoz, Renato Puppi
    PARKINSONISM & RELATED DISORDERS, 2018, 46 : 3 - 8
  • [36] Conditioning in identical twins with ataxia-telangiectasia
    Mostofsky, SH
    Green, JT
    Meginley, M
    Christensen, JR
    Woodruff-Pak, DS
    NEUROCASE, 1999, 5 (05) : 425 - 433
  • [37] The role of epigenomics in the neurodegeneration of ataxia-telangiectasia
    Li, Jiali
    Jiang, Dewei
    EPIGENOMICS, 2015, 7 (02) : 137 - 141
  • [38] Dysfunction of cerebellar microglia in Ataxia-telangiectasia
    Levi, Hadar
    Bar, Ela
    Cohen-Adiv, Stav
    Sweitat, Suzan
    Kanner, Sivan
    Galron, Ronit
    Mitiagin, Yulia
    Barzilai, Ari
    GLIA, 2022, 70 (03) : 536 - 557
  • [39] Testicular seminoma in a patient with ataxia-telangiectasia
    Phillips, HA
    Howard, GCW
    CLINICAL ONCOLOGY, 1999, 11 (01) : 63 - 64
  • [40] Update on the management of the immunodeficiency in ataxia-telangiectasia
    Davies, E. Graham
    EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2009, 5 (05) : 565 - 575