Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)

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Darabi , H , Beesley , J , Droit , A , Kar , S , Nord , S , Marjaneh , M M , Soucy , P , Michailidou , K , Ghoussaini , M , Wahl , H F , Bolla , M K , Wang , Q , Dennis , J , Alonso , M R , Andrulis , I L , Anton-Culver , H , Arndt , V , Beckmann , M W , Benitez , J , Bogdanova , N V , Bojesen , S E , Brauch , H , Brenner , H , Broeks , A , Bruening , T , Burwinkel , B , Chang-Claude , J , Choi , J-Y , Conroy , D M , Couch , F J , Cox , A , Cross , S S , Czene , K , Devilee , P , Doerk , T , Easton , D F , Fasching , P A , Figueroa , J , Fletcher , O , Flyger , H , Galle , E , Garcia-Closas , M , Giles , G G , Goldberg , M S , Gonzalez-Neira , A , Guenel , P , Haiman , C A , Hallberg , E , Hamann , U , Hartman , M , Hollestelle , A , Hopper , J L , Ito , H , Jakubowska , A , Johnson , N , Kang , D , Khan , S , Kosma , V-M , Kriege , M , Kristensen , V , Lambrechts , D , Le Marchand , L , Lee , S C , Lindblom , A , Lophatananon , A , Lubinski , J , Mannermaa , A , Manoukian , S , Margolin , S , Matsuo , K , Mayes , R , Mckay , J , Meindl , A , Milne , R L , Muir , K , Neuhausen , S L , Nevanlinna , H , Olswold , C , Orr , N , Peterlongo , P , Pita , G , Pylkaes , K , Rudolph , A , Sangrajrang , S , Sawyer , E J , Schmidt , M K , Schmutzler , R K , Seynaeve , C , Shah , M , Shen , C-Y , Shu , X-O , Southey , M C , Stram , D O , Surowy , H , Swerdlow , A , Teo , S H , Tessier , D C , Tomlinson , I , Torres , D , Truong , T , Vachon , C M , Vincent , D , Winqvist , R , Wu , A H , Wu , P-E , Yip , C H , Zheng , W , Pharoah , P D P , Hall , P , Edwards , S L , Simard , J , French , J D , Chenevix-Trench , G & Dunning , A M 2016 , ' Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) ' Scientific Reports , vol. 6 , 32512 . DOI: 10.1038/srep32512

Title: Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Author: Darabi, Hatef; Beesley, Jonathan; Droit, Arnaud; Kar, Siddhartha; Nord, Silje; Marjaneh, Mahdi Moradi; Soucy, Penny; Michailidou, Kyriaki; Ghoussaini, Maya; Wahl, Hanna Fues; Bolla, Manjeet K.; Wang, Qin; Dennis, Joe; Alonso, M. Rosario; Andrulis, Irene L.; Anton-Culver, Hoda; Arndt, Volker; Beckmann, Matthias W.; Benitez, Javier; Bogdanova, Natalia V.; Bojesen, Stig E.; Brauch, Hiltrud; Brenner, Hermann; Broeks, Annegien; Bruening, Thomas; Burwinkel, Barbara; Chang-Claude, Jenny; Choi, Ji-Yeob; Conroy, Don M.; Couch, Fergus J.; Cox, Angela; Cross, Simon S.; Czene, Kamila; Devilee, Peter; Doerk, Thilo; Easton, Douglas F.; Fasching, Peter A.; Figueroa, Jonine; Fletcher, Olivia; Flyger, Henrik; Galle, Eva; Garcia-Closas, Montserrat; Giles, Graham G.; Goldberg, Mark S.; Gonzalez-Neira, Anna; Guenel, Pascal; Haiman, Christopher A.; Hallberg, Emily; Hamann, Ute; Hartman, Mikael; Hollestelle, Antoinette; Hopper, John L.; Ito, Hidemi; Jakubowska, Anna; Johnson, Nichola; Kang, Daehee; Khan, Sofia; Kosma, Veli-Matti; Kriege, Mieke; Kristensen, Vessela; Lambrechts, Diether; Le Marchand, Loic; Lee, Soo Chin; Lindblom, Annika; Lophatananon, Artitaya; Lubinski, Jan; Mannermaa, Arto; Manoukian, Siranoush; Margolin, Sara; Matsuo, Keitaro; Mayes, Rebecca; Mckay, James; Meindl, Alfons; Milne, Roger L.; Muir, Kenneth; Neuhausen, Susan L.; Nevanlinna, Heli; Olswold, Curtis; Orr, Nick; Peterlongo, Paolo; Pita, Guillermo; Pylkaes, Katri; Rudolph, Anja; Sangrajrang, Suleeporn; Sawyer, Elinor J.; Schmidt, Marjanka K.; Schmutzler, Rita K.; Seynaeve, Caroline; Shah, Mitul; Shen, Chen-Yang; Shu, Xiao-Ou; Southey, Melissa C.; Stram, Daniel O.; Surowy, Harald; Swerdlow, Anthony; Teo, Soo H.; Tessier, Daniel C.; Tomlinson, Ian; Torres, Diana; Truong, Therese; Vachon, Celine M.; Vincent, Daniel; Winqvist, Robert; Wu, Anna H.; Wu, Pei-Ei; Yip, Cheng Har; Zheng, Wei; Pharoah, Paul D. P.; Hall, Per; Edwards, Stacey L.; Simard, Jacques; French, Juliet D.; Chenevix-Trench, Georgia; Dunning, Alison M.
Contributor: University of Helsinki, Department of Obstetrics and Gynegology
University of Helsinki, Department of Obstetrics and Gynegology
Date: 2016-09-07
Language: eng
Number of pages: 14
Belongs to series: Scientific Reports
ISSN: 2045-2322
URI: http://hdl.handle.net/10138/167471
Abstract: Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. To identify potential causal variants related to breast cancer risk, we performed a high resolution fine-mapping analysis that involved genotyping 517 SNPs using a custom Illumina iSelect array (iCOGS) followed by imputation of genotypes for 3,134 SNPs in more than 89,000 participants of European ancestry from the Breast Cancer Association Consortium (BCAC). We identified 28 highly correlated common variants, in a 53 Kb region spanning two introns of the STXBP4 gene, that are strong candidates for driving breast cancer risk (lead SNP rs2787486 (OR = 0.92; CI 0.90-0.94; P = 8.96 x 10(-15))) and are correlated with two previously reported risk-associated variants at this locus, SNPs rs6504950 (OR = 0.94, P = 2.04 x 10-09, r(2) = 0.73 with lead SNP) and rs1156287 (OR = 0.93, P = 3.41 x 10(-11), r(2) = 0.83 with lead SNP). Analyses indicate only one causal SNP in the region and several enhancer elements targeting STXBP4 are located within the 53 kb association signal. Expression studies in breast tumor tissues found SNP rs2787486 to be associated with increased STXBP4 expression, suggesting this may be a target gene of this locus.
Subject: SUSCEPTIBILITY LOCI
FUNCTIONAL VARIANTS
HUMAN GENOME
RISK LOCUS
EXPRESSION
ASSOCIATION
CONSORTIUM
ENHANCERS
REVEALS
REGION
3122 Cancers
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