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dc.contributor.authorFletcher, O
dc.contributor.authorDudbridge, F
dc.date.accessioned2020-08-06T14:56:05Z
dc.date.issued2014-10-17
dc.identifier.citationBMC medicine, 2014, 12 pp. 195 - ?
dc.identifier.issn1741-7015
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3921
dc.identifier.eissn1741-7015
dc.identifier.doi10.1186/s12916-014-0195-1
dc.description.abstractGene-environment interactions have the potential to shed light on biological processes leading to disease, identify individuals for whom risk factors are most relevant, and improve the accuracy of epidemiological risk models. We review the progress that has been made in investigating gene-environment interactions in the field of breast cancer. Although several large-scale analyses have been carried out, only a few significant interactions have been reported. One of these, an interaction between CASP8-rs1045485 and alcohol consumption has been replicated, but others have not, including LSP1- rs3817198 and parity, and 1p11.2-rs11249433 and ever being parous. False positive interactions may arise if the gene and environment are correlated and the causal variant is less frequent than the tag SNP. We conclude that while much progress has been made in this area it is still too soon to tell whether gene-environment interactions will fulfil their promise. Before we can make this assessment we will need to replicate (or refute) the reported interactions, identify the causal variants that underlie tag-SNP associations and validate the next generation of epidemiological risk models.
dc.formatElectronic
dc.format.extent195 - ?
dc.languageeng
dc.language.isoeng
dc.publisherBIOMED CENTRAL LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectGenetic Predisposition to Disease
dc.subjectRisk Factors
dc.subjectEnvironment
dc.subjectPregnancy
dc.subjectPolymorphism, Single Nucleotide
dc.subjectFemale
dc.subjectGene-Environment Interaction
dc.titleCandidate gene-environment interactions in breast cancer.
dc.typeJournal Article
dcterms.dateAccepted2014-09-30
rioxxterms.versionofrecord10.1186/s12916-014-0195-1
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2014-10-17
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBMC medicine
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genetic Epidemiology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genetic Epidemiology
pubs.publication-statusPublished
pubs.volume12
pubs.embargo.termsNot known
icr.researchteamFunctional Genetic Epidemiology
dc.contributor.icrauthorFletcher, Olivia


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