Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0037866
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dc.titleReplication and fine mapping for association of the C2orf43, FOXP4, GPRC6A and RFX6 genes with prostate cancer in the Chinese population
dc.contributor.authorLong Q.-Z.
dc.contributor.authorDu Y.-F.
dc.contributor.authorDing X.-Y.
dc.contributor.authorLi X.
dc.contributor.authorSong W.-B.
dc.contributor.authorYang Y.
dc.contributor.authorZhang P.
dc.contributor.authorZhou J.-P.
dc.contributor.authorLiu X.-G.
dc.date.accessioned2019-11-11T06:39:02Z
dc.date.available2019-11-11T06:39:02Z
dc.date.issued2012
dc.identifier.citationLong Q.-Z., Du Y.-F., Ding X.-Y., Li X., Song W.-B., Yang Y., Zhang P., Zhou J.-P., Liu X.-G. (2012). Replication and fine mapping for association of the C2orf43, FOXP4, GPRC6A and RFX6 genes with prostate cancer in the Chinese population. PLoS ONE 7 (5) : e37866. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0037866
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161979
dc.description.abstractBackground: Prostate cancer represents the leading cause of male death across the world. A recent genome-wide association study (GWAS) identified five novel susceptibility loci for prostate cancer in the Japanese population. This study is to replicate and fine map the potential association of these five loci with prostate cancer in the Chinese Han population. Methods: In Phase I of the study, we tested the five single nucleotide polymorphisms (SNPs) which showed the strongest association evidence in the original GWAS in Japanese. The study sample consists of 1,169 Chinese Hans, comprising 483 patients and 686 healthy controls. Then in phase II, flanking SNPs of the successfully replicated SNPs in Phase I were genotyped and tested for association with prostate cancer to fine map those significant association signals. Results: We successfully replicated the association of rs13385191 (located in the C2orf43 gene, P = 8.60×10 -5 ), rs12653946 (P = 1.33×10 -6 ), rs1983891 (FOXP4, P = 6.22×10 -5 ), and rs339331 (GPRC6A/RFX6, P = 1.42×10 -5 ) with prostate cancer. The most significant odds ratio (OR) was recorded as 1.41 (95% confidence interval 1.18-1.68) for rs12653946. Rs9600079 did not show significant association (P = 8.07×10 -2 ) with prostate cancer in this study. The Phase II study refined these association signals, and identified several SNPs showing more significant association with prostate cancer than the very SNPs tested in Phase I. Conclusions: Our results provide further support for association of the C2orf43, FOXP4, GPRC6A and RFX6 genes with prostate cancer in Eastern Asian populations. This study also characterized the novel loci reported in the original GWAS with more details. Further work is still required to determine the functional variations and finally clarify the underlying biological mechanisms. © 2012 Long et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectgenomic DNA
dc.subjectaged
dc.subjectarticle
dc.subjectC2orf43 gene
dc.subjectcancer susceptibility
dc.subjectChinese
dc.subjectcontrolled study
dc.subjectFOXP4 gene
dc.subjectgene locus
dc.subjectgene mapping
dc.subjectgene replication
dc.subjectgenetic association
dc.subjectgenotype
dc.subjecthuman
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectoncogene
dc.subjectprostate cancer
dc.subjectRFX6 gene
dc.subjectsingle nucleotide polymorphism
dc.subjectAged
dc.subjectAsian Continental Ancestry Group
dc.subjectCase-Control Studies
dc.subjectChina
dc.subjectChromosome Mapping
dc.subjectDNA Replication
dc.subjectDNA-Binding Proteins
dc.subjectForkhead Transcription Factors
dc.subjectGenome-Wide Association Study
dc.subjectHumans
dc.subjectLinkage Disequilibrium
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeoplasm Proteins
dc.subjectPolymorphism, Single Nucleotide
dc.subjectProstatic Neoplasms
dc.subjectReceptors, G-Protein-Coupled
dc.subjectTranscription Factors
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1371/journal.pone.0037866
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue5
dc.description.pagee37866
dc.published.statePublished
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