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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Ferreira, Manuel A; Gamazon, Eric R; Al-Ejeh, Fares; Aittomaki, Kristiina; Andrulis, Irene L; Anton-Culver, Hoda; Arason, Adalgeir; Arndt, Volker; Aronson, Kristan J; Arun, Banu K; Dahlstrom, Jane

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Genome-wide association studies (GWAS) have identified more than 170 breast cancer susceptibility loci. Here we hypothesize that some risk-associated variants might act in nonbreast tissues, specifically adipose tissue and immune cells from blood and spleen. Using expression quantitative trait loci (eQTL) reported in these tissues, we identify 26 previously unreported, likely target genes of overall breast cancer risk variants, and 17 for estrogen receptor (ER)-negative breast cancer, several...[Show more]

dc.contributor.authorFerreira, Manuel A
dc.contributor.authorGamazon, Eric R
dc.contributor.authorAl-Ejeh, Fares
dc.contributor.authorAittomaki, Kristiina
dc.contributor.authorAndrulis, Irene L
dc.contributor.authorAnton-Culver, Hoda
dc.contributor.authorArason, Adalgeir
dc.contributor.authorArndt, Volker
dc.contributor.authorAronson, Kristan J
dc.contributor.authorArun, Banu K
dc.contributor.authorDahlstrom, Jane
dc.date.accessioned2022-06-07T04:44:31Z
dc.date.available2022-06-07T04:44:31Z
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1885/267187
dc.description.abstractGenome-wide association studies (GWAS) have identified more than 170 breast cancer susceptibility loci. Here we hypothesize that some risk-associated variants might act in nonbreast tissues, specifically adipose tissue and immune cells from blood and spleen. Using expression quantitative trait loci (eQTL) reported in these tissues, we identify 26 previously unreported, likely target genes of overall breast cancer risk variants, and 17 for estrogen receptor (ER)-negative breast cancer, several with a known immune function. We determine the directional effect of gene expression on disease risk measured based on single and multiple eQTL. In addition, using a gene-based test of association that considers eQTL from multiple tissues, we identify seven (and four) regions with variants associated with overall (and ER-negative) breast cancer risk, which were not reported in previous GWAS. Further investigation of the function of the implicated genes in breast and immune cells may provide insights into the etiology of breast cancer.
dc.format.mimetypeapplication/pdf
dc.language.isoen_AU
dc.publisherMacmillan Publishers Ltd
dc.rights© 2019 The authors
dc.rights.urihttp://creativeco mmons.org/licenses/by/4.0/
dc.sourceNature Communications
dc.titleGenome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume10
dc.date.issued2019
local.identifier.absfor111201 - Cancer Cell Biology
local.identifier.ariespublicationu3102795xPUB4936
local.publisher.urlhttps://www.nature.com/
local.type.statusPublished Version
local.contributor.affiliationFerreira, Manuel A, QIMR Berghofer Medical Research Institute
local.contributor.affiliationGamazon, Eric R, Vanderbilt University
local.contributor.affiliationAl-Ejeh, Fares, QIMR Berghofer Medical Research Institute
local.contributor.affiliationAittomaki, Kristiina, Helsinki University Hospital, University of Helsinki
local.contributor.affiliationAndrulis, Irene L, Lunenfeld-Tanenbaum Research Institute of Mount Sinai Hospital
local.contributor.affiliationAnton-Culver, Hoda, Genetic Epidemiology Research Institute, University of California Irvine
local.contributor.affiliationArason, Adalgeir, Landspitali University Hospital
local.contributor.affiliationArndt, Volker, German Cancer Research Center (DKFZ)
local.contributor.affiliationAronson, Kristan J, Queen's University
local.contributor.affiliationArun, Banu K, University of Texas MD Anderson Cancer Center
local.contributor.affiliationDahlstrom, Jane, College of Health and Medicine, ANU
local.bibliographicCitation.startpage1
local.bibliographicCitation.lastpage18
local.identifier.doi10.1038/s41467-018-08053-5
local.identifier.absseo920102 - Cancer and Related Disorders
dc.date.updated2021-01-17T07:18:51Z
local.identifier.thomsonIDWOS:000464494100010
dcterms.accessRightsOpen Access
dc.provenanceOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/ licenses/by/4.0/.
dc.rights.licensecreative commons
CollectionsANU Research Publications

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