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dc.contributor.authorFeng, Y
dc.contributor.authorWang, Y
dc.contributor.authorLiu, H
dc.contributor.authorLiu, Z
dc.contributor.authorMills, C
dc.contributor.authorHan, Y
dc.contributor.authorHung, RJ
dc.contributor.authorBrhane, Y
dc.contributor.authorMcLaughlin, J
dc.contributor.authorBrennan, P
dc.contributor.authorBickeboeller, H
dc.contributor.authorRosenberger, A
dc.contributor.authorHoulston, RS
dc.contributor.authorCaporaso, NE
dc.contributor.authorTeresa Landi, M
dc.contributor.authorBrueske, I
dc.contributor.authorRisch, A
dc.contributor.authorYe, Y
dc.contributor.authorWu, X
dc.contributor.authorChristiani, DC
dc.contributor.authorAmos, CI
dc.contributor.authorWei, Q
dc.date.accessioned2020-10-21T13:34:00Z
dc.date.issued2017-04-11
dc.identifier.citationScientific reports, 2017, 7 (1), pp. 825 - ?
dc.identifier.issn2045-2322
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4182
dc.identifier.eissn2045-2322
dc.identifier.doi10.1038/s41598-017-00850-0
dc.description.abstractThe T-cell protein tyrosine phosphatase (TCPTP) pathway consists of signaling events mediated by TCPTP. Mutations and genetic variants of some genes in the TCPTP pathway are associated with lung cancer risk and survival. In the present study, we first investigated associations of 5,162 single nucleotide polymorphisms (SNPs) in 43 genes of this TCPTP pathway with lung cancer risk by using summary data of six published genome-wide association studies (GWAS) of 12,160 cases and 16,838 controls. We identified 11 independent SNPs in eight genes after correction for multiple comparisons by a false discovery rate <0.20. Then, we performed in silico functional analyses for these 11 SNPs by eQTL analysis, two of which, PTPN2 SNPs rs2847297 and rs2847282, were chosen as tagSNPs. We further included two additional GWAS datasets of Harvard University (984 cases and 970 controls) and deCODE (1,319 cases and 26,380 controls), and the overall effects of these two SNPs among all eight GWAS studies remained significant (OR = 0.95, 95% CI = 0.92-0.98, and P = 0.004 for rs2847297; OR = 0.95, 95% CI = 0.92-0.99, and P = 0.009 for rs2847282). In conclusion, the PTPN2 rs2847297 and rs2847282 may be potential susceptible loci for lung cancer risk.
dc.formatElectronic
dc.format.extent825 - ?
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectLung Neoplasms
dc.subjectPolymorphism, Single Nucleotide
dc.subjectProtein Tyrosine Phosphatase, Non-Receptor Type 2
dc.subjectGenome-Wide Association Study
dc.titleGenetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium.
dc.typeJournal Article
dcterms.dateAccepted2017-03-15
rioxxterms.versionofrecord10.1038/s41598-017-00850-0
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-04-11
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfScientific reports
pubs.issue1
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/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genomics
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/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genomics
pubs.publication-statusPublished
pubs.volume7
pubs.embargo.termsNot known
icr.researchteamCancer Genomicsen_US
dc.contributor.icrauthorHoulston, Richarden


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