Is a Susceptibility Locus for Hormone Receptor Positive Breast Cancer

Diether Lambrechts,Thérèse Truong,Christina Justenhoven,Manjeet K. Humphreys, Jianghai Wang,John L Hopper,Gillian S Dite,Carmel Apicella,Melissa C. Southey,Marjanka K. Schmidt,Annegien Broeks, Sten Cornelissen, Richard R van Hien,Elinor J Sawyer,Ian Tomlinson,Michael J. Kerin,Nicola Miller,Roger L. Milne,M. Pilar Zamora,José Ignacio Arias Pérez,Javier Benítez,Ute Hamann,Y. Ko,Thomas Brüning,Jenny Chang-Claude,Ursel Eilber,Rebecca Hein,Stefan Nickels,Dieter Flesch-Janys,Shan Wang-Gohrke,Esther M John,Alexander Miron,Robert Winqvist,Katri Pylkäs,Arja Jukkola-Vuorinen,Georgia Chenevix-Trench,Jonathan Beesley,Florence Menegaux,Emilie Cordina-Duverger,Chen-Yang Shen,Jyh-Cherng Yu,Pei-Ei Wu,Ming-Feng Hou,Irene L. Andrulis, Teresa Selander,Gord Glendon,Anna Marie Mulligan,Hoda Anton-Culver,Argyrios Ziogas,Kenneth R. Muir,Artitaya Lophatananon,Suthee Rattanamongkongul,Puttisak Puttawibul, Meinir Jones,Nicholas Orr,Alan Ashworth,Anthony Swerdlow,Gianluca Severi,Laura Baglietto,Graham G. Giles,Melissa C. Southey,Federik Marmé,Andreas Schneeweiss,Christof Sohn,Barbara Burwinkel,Betul T. Yesilyurt,Patrick Neven, Robert J Paridaens,Hans Wildiers,Hermann Brenner,Heiko Mueller,Volker Arndt,Christa Stegmaier,Alfons Meindl,Sarah Schott, Claus Rainer Bartram,Rita Schmutzler,Angela Cox,Ian Wallace Brock,Graeme Elliott,Simon S. Cross,Peter A. Fasching,Rüdiger Schulz-Wendtland,Arif B. Ekici, Matthias Wilhelm Beckmann,Olivia Fletcher,Nichola Johnson,Isabel dos Santos Silva,Julian Peto,Heli Nevanlinna,Taru A. Muranen,Kristiina Aittomäki,Carl Blomqvist,Thilo Dörk,Peter Schürmann,Michael Bremer,Peter Hillemanns, Natalia V. Bogdanova,Natalia N. Antonenkova,Yuri I. Rogov,Johann Hinrich Karstens,Elza Khusnutdinova, Marina Bermisheva, Darya Prokofieva,Shamil Gancev,Anna Jakubowska,Jan Lubiński, Katarzyna Jaworska,Katarzyna Durda,Børge G. Nordestgaard,Stig E. Bojesen, Charlotte Lanng,Arto Mannermaa,Vesa Kataja,Veli‐Matti Kosma,Jaana M. Hartikainen,Paolo Radice,Paolo Peterlongo,Siranoush Manoukian,Loris Bernard,Fergus J Couch,Janet E. Olson,Xianshu Wang,Zachary S. Fredericksen,Grethe I. Grenaker Alnæs,Vessela N. Kristensen,Anne-Lise Børresen-Dale,Peter Devilee, Robert A.E.M. Tollenaar, Caroline M. Seynaeve,Jolanta Lissowska,Kamila Czene,Daehee Kang,Annika Lindblom,Sara Margolin,Alison M. Dunning,Paul D. P. Pharoah,Douglas F. Easton,Pascal Guénel,Hiltrud Brauch

semanticscholar(2017)

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摘要
A recent two-stage genome-wide association study (GWAS) identified five novel breast cancer susceptibility loci on chromosomes 9, 10, and 11. To provide more reliable estimates of the relative risk associated with these loci and investigate possible heterogeneity by subtype of breast cancer, we genotyped the variants rs2380205, rs1011970, rs704010, rs614367, and rs10995190 in 39 studies from the Breast Cancer Association Consortium (BCAC), involving 49,608 cases and 48,772 controls of predominantly European ancestry. Four of the variants showed clear evidence of association (P ≤ 3 × 10−9) and weak evidence was observed for rs2380205 (P = 0.06). The strongest evidence was obtained for rs614367, located on 11q13 (per-allele odds ratio 1.21, P = 4 × 10−39). The association for rs614367 was specific to estrogen receptor (ER)-positive disease and strongest for ER plus progesterone receptor (PR)-positive breast cancer, whereas the associations for the other three loci did not differ by tumor subtype. Hum Mutat 33:1123–1132, 2012. C © 2012 Wiley Periodicals, Inc.
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