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dc.contributor.authorPing, J
dc.contributor.authorJia, G
dc.contributor.authorCai, Q
dc.contributor.authorGuo, X
dc.contributor.authorTao, R
dc.contributor.authorAmbrosone, C
dc.contributor.authorHuo, D
dc.contributor.authorAmbs, S
dc.contributor.authorBarnard, ME
dc.contributor.authorChen, Y
dc.contributor.authorGarcia-Closas, M
dc.contributor.authorGu, J
dc.contributor.authorHu, JJ
dc.contributor.authorJohn, EM
dc.contributor.authorLi, CI
dc.contributor.authorNathanson, K
dc.contributor.authorNemesure, B
dc.contributor.authorOlopade, OI
dc.contributor.authorPal, T
dc.contributor.authorPress, MF
dc.contributor.authorSanderson, M
dc.contributor.authorSandler, DP
dc.contributor.authorYoshimatsu, T
dc.contributor.authorAdejumo, PO
dc.contributor.authorAhearn, T
dc.contributor.authorBrewster, AM
dc.contributor.authorHennis, AJM
dc.contributor.authorMakumbi, T
dc.contributor.authorNdom, P
dc.contributor.authorO'Brien, KM
dc.contributor.authorOlshan, AF
dc.contributor.authorOluwasanu, MM
dc.contributor.authorReid, S
dc.contributor.authorYao, S
dc.contributor.authorButler, EN
dc.contributor.authorHuang, M
dc.contributor.authorNtekim, A
dc.contributor.authorLi, B
dc.contributor.authorTroester, MA
dc.contributor.authorPalmer, JR
dc.contributor.authorHaiman, CA
dc.contributor.authorLong, J
dc.contributor.authorZheng, W
dc.coverage.spatialEngland
dc.date.accessioned2024-07-30T14:29:13Z
dc.date.available2024-07-30T14:29:13Z
dc.date.issued2024-05-02
dc.identifierARTN 3718
dc.identifier10.1038/s41467-024-47650-5
dc.identifier.citationNature Communications, 2024, 15 (1), pp. 3718 -en_US
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6328
dc.identifier.eissn2041-1723
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-024-47650-5
dc.identifier.doi10.1038/s41467-024-47650-5
dc.description.abstractAfrican-ancestry (AA) participants are underrepresented in genetics research. Here, we conducted a transcriptome-wide association study (TWAS) in AA female participants to identify putative breast cancer susceptibility genes. We built genetic models to predict levels of gene expression, exon junction, and 3' UTR alternative polyadenylation using genomic and transcriptomic data generated in normal breast tissues from 150 AA participants and then used these models to perform association analyses using genomic data from 18,034 cases and 22,104 controls. At Bonferroni-corrected P < 0.05, we identified six genes associated with breast cancer risk, including four genes not previously reported (CTD-3080P12.3, EN1, LINC01956 and NUP210L). Most of these genes showed a stronger association with risk of estrogen-receptor (ER) negative or triple-negative than ER-positive breast cancer. We also replicated the associations with 29 genes reported in previous TWAS at P < 0.05 (one-sided), providing further support for an association of these genes with breast cancer risk. Our study sheds new light on the genetic basis of breast cancer and highlights the value of conducting research in AA populations.
dc.formatElectronic
dc.format.extent3718 -
dc.languageeng
dc.language.isoengen_US
dc.publisherNATURE PORTFOLIOen_US
dc.relation.ispartofNature Communications
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectAdult
dc.subjectAged
dc.subjectFemale
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectBlack People
dc.subjectBreast Neoplasms
dc.subjectCase-Control Studies
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectGenetic Predisposition to Disease
dc.subjectGenome-Wide Association Study
dc.subjectPolymorphism, Single Nucleotide
dc.subjectReceptors, Estrogen
dc.subjectTranscriptome
dc.subjectBlack or African American
dc.subjectUnited States
dc.titleUsing genome and transcriptome data from African-ancestry female participants to identify putative breast cancer susceptibility genes.en_US
dc.typeJournal Article
dcterms.dateAccepted2024-04-08
dc.date.updated2024-07-30T14:28:46Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1038/s41467-024-47650-5en_US
rioxxterms.licenseref.startdate2024-05-02
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38697998
pubs.issue1
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Integrative Cancer Epidemiology
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1038/s41467-024-47650-5
pubs.volume15
icr.researchteamIntegrative Cancer Epidemen_US
dc.contributor.icrauthorGarcia-Closas, Montserrat
icr.provenanceDeposited by Mr Arek Surman on 2024-07-30. Deposit type is initial. No. of files: 1. Files: Using genome and transcriptome data from African-ancestry female participants to identify putative breast cancer susceptibil.pdf


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