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    The effect on melanoma risk of genes previously associated with telomere length

    Access Status
    Open access via publisher
    Authors
    Iles, M.
    Bishop, D.
    Taylor, J.
    Hayward, N.
    Brossard, M.
    Cust, A.
    Dunning, A.
    Lee, J.
    Moses, Eric
    Akslen, L.
    Andresen, P.
    Avril, M.
    Azizi, E.
    Scarra, G.
    Brown, K.
    Debniak, T.
    Elder, D.
    Friedman, E.
    Ghiorzo, P.
    Gillanders, E.
    Goldstein, A.
    Gruis, N.
    Hansson, J.
    Harland, M.
    Helsing, P.
    Hoçevar, M.
    Hoiom, V.
    Ingvar, C.
    Kanetsky, P.
    Landi, M.
    Lang, J.
    Lathrop, G.
    Lubinski, J.
    Mackie, R.
    Martin, N.
    Molven, A.
    Montgomery, G.
    Novakovi, S.
    Olsson, H.
    Puig, S.
    Puig-Butille, J.
    Radford-Smith, G.
    Randerson-Moor, J.
    Van Der Stoep, N.
    Van Doorn, R.
    Whiteman, D.
    Macgregor, S.
    Pooley, K.
    Ward, S.
    Mann, G.
    Amos, C.
    Pharoah, P.
    Demenais, F.
    Law, M.
    Bishop, J.
    Barrett, J.
    Date
    2014
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Iles, M. and Bishop, D. and Taylor, J. and Hayward, N. and Brossard, M. and Cust, A. and Dunning, A. et al. 2014. The effect on melanoma risk of genes previously associated with telomere length. Journal of the National Cancer Institute. 106 (10): dju267.
    Source Title
    Journal of the National Cancer Institute
    DOI
    10.1093/jnci/dju267
    ISSN
    0027-8874
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/40881
    Collection
    • Curtin Research Publications
    Abstract

    Telomere length has been associated with risk of many cancers, but results are inconsistent. Seven single nucleotide polymorphisms (SNPs) previously associated with mean leukocyte telomere length were either genotyped or well-imputed in 11108 case patients and 13933 control patients from Europe, Israel, the United States and Australia, four of the seven SNPs reached a P value under .05 (two-sided). A genetic score that predicts telomere length, derived from these seven SNPs, is strongly associated (P = 8.92x10-9, two-sided) with melanoma risk. This demonstrates that the previously observed association between longer telomere length and increased melanoma risk is not attributable to confounding via shared environmental effects (such as ultraviolet exposure) or reverse causality. We provide the first proof that multiple germline genetic determinants of telomere length influence cancer risk.

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