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Ji, X.* ; Mukherjee, S.* ; Landi, M.T.* ; Bosse, Y.* ; Joubert, P.* ; Zhu, D.* ; Gorlov, I.* ; Xiao, X.* ; Han, Y.* ; Gorlova, O.* ; Hung, R.J.* ; Brhane, Y.* ; Carreras-Torres, R.* ; Christiani, D.C.* ; Caporaso, N.* ; Johansson, M.* ; Liu, G.* ; Bojesen, S.E.* ; Le Marchand, L.* ; Albanes, D.* ; Bickeböller, H.* ; Aldrich, M.C.* ; Bush, W.S.* ; Tardón, A.* ; Rennert, G.* ; Chen, C.* ; Byun, J.* ; Dragnev, K.H.* ; Field, J.K.* ; Kiemeney, L.F.* ; Lazarus, P.* ; Zienolddiny, S.* ; Lam, S.* ; Schabath, M.B.* ; Andrew, A.S.* ; Bertazzi, P.A.* ; Pesatori, A.C.* ; Diao, N.* ; Su, L.* ; Song, L.* ; Zhang, R.* ; Leighl, N.* ; Johansen, J.S.* ; Mellemgaard, A.* ; Saliba, W.* ; Haiman, C.* ; Wilkens, L.* ; Fernández-Somoano, A.* ; Fernandez-Tardon, G.* ; Heijden, E.H.F.M.v.d.* ; Kim, J.H.* ; Davies, M.P.A.* ; Marcus, M.W.* ; Brunnström, H.* ; Manjer, J.* ; Melander, O.* ; Müller, D.C.* ; Overvad, K.* ; Trichopoulou, A.* ; Tumino, R.* ; Goodman, G.E.* ; Cox, A.* ; Taylor, F.* ; Woll, P.* ; Wichmann, H.-E. ; Muley, T.* ; Risch, A.* ; Rosenberger, A.* ; Grankvist, K.* ; Shepherd, F.A.* ; Tsao, M.S.* ; Arnold, S.M.* ; Haura, E.B.* ; Bolca, C.* ; Holcatova, I.* ; Janout, V.* ; Kontic, M.* ; Lissowska, J.* ; Mukeria, A.* ; Ognjanovic, S.* ; Orlowski, T.M.* ; Scelo, G.* ; Swiatkowska, B.* ; Zaridze, D.* ; Bakke, P.* ; Skaug, V.* ; Butler, L.M.* ; Offit, K.* ; Srinivasan, P.* ; Bandlamudi, C.* ; Hellmann, M.D.* ; Solit, D.B.* ; Robson, M.E.* ; Rudin, C.M.* ; Stadler, Z.K.* ; Taylor, B.S.* ; Berger, M.F.* ; Houlston, R.* ; McLaughlin, J.*

Protein-altering germline mutations implicate novel genes related to lung cancer development.

Nat. Commun. 11:2220 (2020)
Verlagsversion Forschungsdaten DOI
Open Access Gold
Creative Commons Lizenzvertrag
Few germline mutations are known to affect lung cancer risk. We performed analyses of rare variants from 39,146 individuals of European ancestry and investigated gene expression levels in 7,773 samples. We find a large-effect association with an ATM L2307F (rs56009889) mutation in adenocarcinoma for discovery (adjusted Odds Ratio=8.82, P=1.18x10(-15)) and replication (adjusted OR=2.93, P=2.22x10(-3)) that is more pronounced in females (adjusted OR=6.81 and 3.19 and for discovery and replication). We observe an excess loss of heterozygosity in lung tumors among ATM L2307F allele carriers. L2307F is more frequent (4%) among Ashkenazi Jewish populations. We also observe an association in discovery (adjusted OR=2.61, P=7.98x10(-22)) and replication datasets (adjusted OR=1.55, P=0.06) with a loss-of-function mutation, Q4X (rs150665432) of an uncharacterized gene, KIAA0930. Our findings implicate germline genetic variants in ATM with lung cancer susceptibility and suggest KIAA0930 as a novel candidate gene for lung cancer risk. In lung cancer, relatively few germline mutations are known to impact risk. Here the authors looked at rare variants in 39,146 individuals and find novel germline mutations associated with risk, as well as implicating ATM and a new candidate gene for lung cancer risk.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Association; Susceptibility; Expression; Prediction; Brca1
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 11, Heft: 1, Seiten: , Artikelnummer: 2220 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed