Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

Author(s): Schumacher FR,  Schmit SL,  Jiao S,  Edlund CK,  Wang H,  Zhang B,  Hsu L,  Huang SC,  Fischer CP,  Harju JF,  Idos GE,  Lejbkowicz F,  Manion FJ,  McDonnell K,  McNeil CE,  Melas M,  Rennert HS,  Shi W,  Thomas DC,  Van Den Berg DJ,  Hutter CM,  Aragaki AK,  Butterbach K,  Caan BJ,  Carlson CS,  Chanock SJ,  Curtis KR,  Fuchs CS,  Gala M,  Giovannucci EL,  Gogarten SM,  Hayes RB,  Henderson B,  Hunter DJ,  Jackson RD,  Kolonel LN,  Kooperberg C,  Küry S,  LaCroix A,  Laurie CC,  Laurie CA,  Lemire M,  Levine D,  Ma J,  Makar KW,  Qu C,  Taverna D,  Ulrich CM,  Wu K,  Kono S,  West DW,  Berndt SI,  Bezieau S,  Brenner H,  Campbell PT,  Chan AT,  Chang-Claude J,  Coetzee GA,  Conti DV,  Duggan D,  Figueiredo JC,  Fortini BK,  Gallinger SJ,  Gauderman WJ,  Giles G,  Green R,  Haile R,  Harrison TA,  Hoffmeister M,  Hopper JL,  Hudson TJ,  Jacobs E,  Iwasaki M,  Jee SH,  Jenkins M,  Jia WH,  Joshi A,  Li L,  Lindor NM,  Matsuo K,  Moreno V,  Mukherjee B,  Newcomb PA,  Potter JD,  Raskin L,  Rennert G,  Rosse S,  Severi G,  Schoen RE,  Seminara D,  Shu XO,  Slattery ML,  Tsugane S,  White E,  Xiang YB,  Zanke BW,  Zheng W,  Le Marchand L,  Casey G,  Gruber SB,  Peters U

Journal: Nat Commun

Date: 2015 Jul 7

Major Program(s) or Research Group(s): PLCO

PubMed ID: 26151821

PMC ID: PMC4967357

Abstract: Genetic susceptibility to colorectal cancer is caused by rare pathogenic mutations and common genetic variants that contribute to familial risk. Here we report the results of a two-stage association study with 18,299 cases of colorectal cancer and 19,656 controls, with follow-up of the most statistically significant genetic loci in 4,725 cases and 9,969 controls from two Asian consortia. We describe six new susceptibility loci reaching a genome-wide threshold of P<5.0E-08. These findings provide additional insight into the underlying biological mechanisms of colorectal cancer and demonstrate the scientific value of large consortia-based genetic epidemiology studies.