Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

  • Helian Feng
  • Alexander Gusev
  • Bogdan Pasaniuc
  • Lang Wu
  • Jirong Long
  • Zomoroda Abu-Full
  • Kristiina Aittomäki
  • Irene L Andrulis
  • Hoda Anton-Culver
  • Antonis C Antoniou
  • Adalgeir Arason
  • Volker Arndt
  • Kristan J Aronson
  • Banu K Arun
  • Ella Asseryanis
  • Paul L Auer
  • Jacopo Azzollini
  • Judith Balmaña
  • Rosa B Barkardottir
  • Daniel R Barnes
  • Daniel Barrowdale
  • Sabine Behrens
  • Javier Benitez
  • Marina Bermisheva
  • Katarzyna Białkowska
  • Ana Blanco
  • Carl Blomqvist
  • Bram Boeckx
  • Natalia V Bogdanova
  • Stig E Bojesen
  • Manjeet K Bolla
  • Bernardo Bonanni
  • Ake Borg
  • Hiltrud Brauch
  • Hermann Brenner
  • Ignacio Briceno
  • Annegien Broeks
  • Thomas Brüning
  • Barbara Burwinkel
  • Qiuyin Cai
  • Trinidad Caldés
  • Maria A Caligo
  • Ian Campbell
  • Sander Canisius
  • Daniele Campa
  • Brian D Carter
  • Jonathan Carter
  • Jose E Castelao
  • Jenny Chang-Claude
  • Stephen J Chanock
  • Hans Christiansen
  • Wendy K Chung
  • Kathleen B M Claes
  • Christine L Clarke
  • Fergus J Couch
  • Angela Cox
  • Simon S Cross
  • Cezary Cybulski
  • Kamila Czene
  • Mary B Daly
  • Miguel de la Hoya
  • Kim De Leeneer
  • Joe Dennis
  • Peter Devilee
  • Orland Diez
  • Susan M Domchek
  • Thilo Dörk
  • Isabel Dos-Santos-Silva
  • Alison M Dunning
  • Miriam Dwek
  • Diana M Eccles
  • Bent Ejlertsen
  • Carolina Ellberg
  • Christoph Engel
  • Mikael Eriksson
  • Peter A Fasching
  • Olivia Fletcher
  • Henrik Flyger
  • Florentia Fostira
  • Eitan Friedman
  • Lin Fritschi
  • Debra Frost
  • Marike Gabrielson
  • Patricia A Ganz
  • Susan M Gapstur
  • Judy Garber
  • Montserrat García-Closas
  • José A García-Sáenz
  • Mia M Gaudet
  • Graham G Giles
  • Gord Glendon
  • Andrew K Godwin
  • Mark S Goldberg
  • David E Goldgar
  • Anna González-Neira
  • Mark H Greene
  • Jacek Gronwald
  • Pascal Guénel
  • Christopher A Haiman
  • Per Hall
  • Ute Hamann
  • Christopher Hake
  • Wei He
  • Jane Heyworth
  • Frans B L Hogervorst
  • Antoinette Hollestelle
  • Maartje J Hooning
  • Robert N Hoover
  • John L Hopper
  • Guanmengqian Huang
  • Peter J Hulick
  • Keith Humphreys
  • Evgeny N Imyanitov
  • Claudine Isaacs
  • Milena Jakimovska
  • Anna Jakubowska
  • Paul James
  • Ramunas Janavicius
  • Rachel C Jankowitz
  • Esther M John
  • Nichola Johnson
  • Vijai Joseph
  • Audrey Jung
  • Beth Y Karlan
  • Elza Khusnutdinova
  • Johanna I Kiiski
  • Irene Konstantopoulou
  • Vessela N Kristensen
  • Yael Laitman
  • Diether Lambrechts
  • Conxi Lazaro
  • Dominique Leroux
  • Goska Leslie
  • Jenny Lester
  • Fabienne Lesueur
  • Noralane Lindor
  • Sara Lindström
  • Wing-Yee Lo
  • Jennifer T Loud
  • Jan Lubiński
  • Enes Makalic
  • Arto Mannermaa
  • Mehdi Manoochehri
  • Siranoush Manoukian
  • Sara Margolin
  • John W M Martens
  • Maria E Martinez
  • Laura Matricardi
  • Tabea Maurer
  • Dimitrios Mavroudis
  • Lesley McGuffog
  • Alfons Meindl
  • Usha Menon
  • Kyriaki Michailidou
  • Pooja M Kapoor
  • Austin Miller
  • Marco Montagna
  • Fernando Moreno
  • Lidia Moserle
  • Anna M Mulligan
  • Taru A Muranen
  • Katherine L Nathanson
  • Susan L Neuhausen
  • Heli Nevanlinna
  • Ines Nevelsteen
  • Finn C Nielsen
  • Liene Nikitina-Zake
  • Kenneth Offit
  • Edith Olah
  • Olufunmilayo I Olopade
  • Håkan Olsson
  • Ana Osorio
  • Janos Papp
  • Tjoung-Won Park-Simon
  • Michael T Parsons
  • Inge S Pedersen
  • Ana Peixoto
  • Paolo Peterlongo
  • Julian Peto
  • Paul D P Pharoah
  • Kelly-Anne Phillips
  • Dijana Plaseska-Karanfilska
  • Bruce Poppe
  • Nisha Pradhan
  • Karolina Prajzendanc
  • Nadege Presneau
  • Kevin Punie
  • Katri Pylkäs
  • Paolo Radice
  • Johanna Rantala
  • Muhammad Usman Rashid
  • Gad Rennert
  • Harvey A Risch
  • Mark Robson
  • Atocha Romero
  • Emmanouil Saloustros
  • Dale P Sandler
  • Catarina Santos
  • Elinor J Sawyer
  • Marjanka K Schmidt
  • Daniel F Schmidt
  • Rita K Schmutzler
  • Minouk J Schoemaker
  • Rodney J Scott
  • Priyanka Sharma
  • Xiao-Ou Shu
  • Jacques Simard
  • Christian F Singer
  • Anne-Bine Skytte
  • Penny Soucy
  • Melissa C Southey
  • John J Spinelli
  • Amanda B Spurdle
  • Jennifer Stone
  • Anthony J Swerdlow
  • William J Tapper
  • Jack A Taylor
  • Manuel R Teixeira
  • Mary Beth Terry
  • Alex Teulé
  • Mads Thomassen
  • Kathrin Thöne
  • Darcy L Thull
  • Marc Tischkowitz
  • Amanda E Toland
  • Rob A E M Tollenaar
  • Diana Torres
  • Thérèse Truong
  • Nadine Tung
  • Celine M Vachon
  • Christi J van Asperen
  • Ans M W van den Ouweland
  • Elizabeth J van Rensburg
  • Ana Vega
  • Alessandra Viel
  • Paula Vieiro-Balo
  • Qin Wang
  • Barbara Wappenschmidt
  • Clarice R Weinberg
  • Jeffrey N Weitzel
  • Camilla Wendt
  • Robert Winqvist
  • Xiaohong R Yang
  • Drakoulis Yannoukakos
  • Argyrios Ziogas
  • Roger L Milne
  • Douglas F Easton
  • Georgia Chenevix-Trench
  • Wei Zheng
  • Peter Kraft
  • Xia Jiang
  • GEMO Study Collaborators

Beteiligte Einrichtungen

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.

Bibliografische Daten

OriginalspracheEnglisch
ISSN0741-0395
DOIs
StatusVeröffentlicht - 07.2020

Anmerkungen des Dekanats

© 2020 The Authors. Genetic Epidemiology published by Wiley Periodicals, Inc.

PubMed 32115800