- Main
Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status
- Feng, Helian;
- Gusev, Alexander;
- Pasaniuc, Bogdan;
- Wu, Lang;
- Long, Jirong;
- Abu‐full, Zomoroda;
- Aittomäki, Kristiina;
- Andrulis, Irene L;
- Anton‐Culver, Hoda;
- Antoniou, Antonis C;
- Arason, Adalgeir;
- Arndt, Volker;
- Aronson, Kristan J;
- Arun, Banu K;
- Asseryanis, Ella;
- Auer, Paul L;
- Azzollini, Jacopo;
- Balmaña, Judith;
- Barkardottir, Rosa B;
- Barnes, Daniel R;
- Barrowdale, Daniel;
- Beckmann, Matthias W;
- Behrens, Sabine;
- Benitez, Javier;
- Bermisheva, Marina;
- Białkowska, Katarzyna;
- Blanco, Ana;
- Blomqvist, Carl;
- Boeckx, Bram;
- Bogdanova, Natalia V;
- Bojesen, Stig E;
- Bolla, Manjeet K;
- Bonanni, Bernardo;
- Borg, Ake;
- Brauch, Hiltrud;
- Brenner, Hermann;
- Briceno, Ignacio;
- Broeks, Annegien;
- Brüning, Thomas;
- Burwinkel, Barbara;
- Cai, Qiuyin;
- Caldés, Trinidad;
- Caligo, Maria A;
- Campbell, Ian;
- Canisius, Sander;
- Campa, Daniele;
- Carter, Brian D;
- Carter, Jonathan;
- Castelao, Jose E;
- Chang‐Claude, Jenny;
- Chanock, Stephen J;
- Christiansen, Hans;
- Chung, Wendy K;
- Claes, Kathleen BM;
- Clarke, Christine L;
- Collaborators, GEMO Study;
- Collaborators, EMBRACE;
- Collaborators, GC‐HBOC study;
- Couch, Fergus J;
- Cox, Angela;
- Cross, Simon S;
- Cybulski, Cezary;
- Czene, Kamila;
- Daly, Mary B;
- de la Hoya, Miguel;
- De Leeneer, Kim;
- Dennis, Joe;
- Devilee, Peter;
- Diez, Orland;
- Domchek, Susan M;
- Dörk, Thilo;
- dos‐Santos‐Silva, Isabel;
- Dunning, Alison M;
- Dwek, Miriam;
- Eccles, Diana M;
- Ejlertsen, Bent;
- Ellberg, Carolina;
- Engel, Christoph;
- Eriksson, Mikael;
- Fasching, Peter A;
- Fletcher, Olivia;
- Flyger, Henrik;
- Fostira, Florentia;
- Friedman, Eitan;
- Fritschi, Lin;
- Frost, Debra;
- Gabrielson, Marike;
- Ganz, Patricia A;
- Gapstur, Susan M;
- Garber, Judy;
- García‐Closas, Montserrat;
- García‐Sáenz, José A;
- Gaudet, Mia M;
- Giles, Graham G;
- Glendon, Gord;
- Godwin, Andrew K;
- Goldberg, Mark S;
- Goldgar, David E;
- González‐Neira, Anna;
- Greene, Mark H;
- Gronwald, Jacek;
- Guénel, Pascal;
- Haiman, Christopher A;
- Hall, Per;
- Hamann, Ute;
- Hake, Christopher;
- He, Wei;
- Heyworth, Jane;
- Hogervorst, Frans BL;
- Hollestelle, Antoinette;
- Hooning, Maartje J;
- Hoover, Robert N;
- Hopper, John L;
- Huang, Guanmengqian;
- Hulick, Peter J;
- Humphreys, Keith;
- Imyanitov, Evgeny N;
- Investigators, ABCTB;
- Investigators, HEBON;
- Investigators, BCFR;
- Investigators, OCGN;
- Isaacs, Claudine;
- Jakimovska, Milena;
- Jakubowska, Anna;
- James, Paul;
- Janavicius, Ramunas;
- Jankowitz, Rachel C;
- John, Esther M;
- Johnson, Nichola;
- Joseph, Vijai;
- Jung, Audrey;
- Karlan, Beth Y;
- Khusnutdinova, Elza;
- Kiiski, Johanna I;
- Konstantopoulou, Irene;
- Kristensen, Vessela N;
- Laitman, Yael;
- Lambrechts, Diether;
- Lazaro, Conxi;
- Leroux, Dominique;
- Leslie, Goska;
- Lester, Jenny;
- Lesueur, Fabienne;
- Lindor, Noralane;
- Lindström, Sara;
- Lo, Wing‐Yee;
- Loud, Jennifer T;
- Lubiński, Jan;
- Makalic, Enes;
- Mannermaa, Arto;
- Manoochehri, Mehdi;
- Manoukian, Siranoush;
- Margolin, Sara;
- Martens, John WM;
- Martinez, Maria E;
- Matricardi, Laura;
- Maurer, Tabea;
- Mavroudis, Dimitrios;
- McGuffog, Lesley;
- Meindl, Alfons;
- Menon, Usha;
- Michailidou, Kyriaki;
- Kapoor, Pooja M;
- Miller, Austin;
- Montagna, Marco;
- Moreno, Fernando;
- Moserle, Lidia;
- Mulligan, Anna M;
- Muranen, Taru A;
- Nathanson, Katherine L;
- Neuhausen, Susan L;
- Nevanlinna, Heli;
- Nevelsteen, Ines;
- Nielsen, Finn C;
- Nikitina‐Zake, Liene;
- Offit, Kenneth;
- Olah, Edith;
- Olopade, Olufunmilayo I;
- Olsson, Håkan;
- Osorio, Ana;
- Papp, Janos;
- Park‐Simon, Tjoung‐Won;
- Parsons, Michael T;
- Pedersen, Inge S;
- Peixoto, Ana;
- Peterlongo, Paolo;
- Peto, Julian;
- Pharoah, Paul DP;
- Phillips, Kelly‐Anne;
- Plaseska‐Karanfilska, Dijana;
- Poppe, Bruce;
- Pradhan, Nisha;
- Prajzendanc, Karolina;
- Presneau, Nadege;
- Punie, Kevin;
- Pylkäs, Katri;
- Radice, Paolo;
- Rantala, Johanna;
- Rashid, Muhammad Usman;
- Rennert, Gad;
- Risch, Harvey A;
- Robson, Mark;
- Romero, Atocha;
- Saloustros, Emmanouil;
- Sandler, Dale P;
- Santos, Catarina;
- Sawyer, Elinor J;
- Schmidt, Marjanka K;
- Schmidt, Daniel F;
- Schmutzler, Rita K;
- Schoemaker, Minouk J;
- Scott, Rodney J;
- Sharma, Priyanka;
- Shu, Xiao‐Ou;
- Simard, Jacques;
- Singer, Christian F;
- Skytte, Anne‐Bine;
- Soucy, Penny;
- Southey, Melissa C;
- Spinelli, John J;
- Spurdle, Amanda B;
- Stone, Jennifer;
- Swerdlow, Anthony J;
- Tapper, William J;
- Taylor, Jack A;
- Teixeira, Manuel R;
- Terry, Mary Beth;
- Teulé, Alex;
- Thomassen, Mads;
- Thöne, Kathrin;
- Thull, Darcy L;
- Tischkowitz, Marc;
- Toland, Amanda E;
- Tollenaar, Rob AEM;
- Torres, Diana;
- Truong, Thérèse;
- Tung, Nadine;
- Vachon, Celine M;
- van Asperen, Christi J;
- van den Ouweland, Ans MW;
- van Rensburg, Elizabeth J;
- Vega, Ana;
- Viel, Alessandra;
- Vieiro‐Balo, Paula;
- Wang, Qin;
- Wappenschmidt, Barbara;
- Weinberg, Clarice R;
- Weitzel, Jeffrey N;
- Wendt, Camilla;
- Winqvist, Robert;
- Yang, Xiaohong R;
- Yannoukakos, Drakoulis;
- Ziogas, Argyrios;
- Milne, Roger L;
- Easton, Douglas F;
- Chenevix‐Trench, Georgia;
- Zheng, Wei;
- Kraft, Peter;
- Jiang, Xia
- et al.
Abstract
Previous transcriptome-wide association studies (TWAS) have identified breast cancer risk genes by integrating data from expression quantitative loci and genome-wide association studies (GWAS), but analyses of breast cancer subtype-specific associations have been limited. In this study, we conducted a TWAS using gene expression data from GTEx and summary statistics from the hitherto largest GWAS meta-analysis conducted for breast cancer overall, and by estrogen receptor subtypes (ER+ and ER-). We further compared associations with ER+ and ER- subtypes, using a case-only TWAS approach. We also conducted multigene conditional analyses in regions with multiple TWAS associations. Two genes, STXBP4 and HIST2H2BA, were specifically associated with ER+ but not with ER- breast cancer. We further identified 30 TWAS-significant genes associated with overall breast cancer risk, including four that were not identified in previous studies. Conditional analyses identified single independent breast-cancer gene in three of six regions harboring multiple TWAS-significant genes. Our study provides new information on breast cancer genetics and biology, particularly about genomic differences between ER+ and ER- breast cancer.
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