Department of Urology, the First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an Shaanxi, People's Republic of China.
PLoS One. 2012;7(5):e37866. doi: 10.1371/journal.pone.0037866. Epub 2012 May 25.
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.
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.
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.
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.
前列腺癌是全球男性死亡的主要原因。最近的全基因组关联研究(GWAS)在日本人群中发现了五个与前列腺癌相关的新易感基因位点。本研究旨在复制并精确定位这些基因位点与中国汉族人群前列腺癌的潜在关联。
在研究的第一阶段,我们测试了在日本原 GWAS 中显示出最强关联证据的五个单核苷酸多态性(SNP)。研究样本包括 1169 名中国汉族人,其中 483 名患者和 686 名健康对照。然后在第二阶段,对第一阶段成功复制的 SNP 的侧翼 SNP 进行基因分型,并测试其与前列腺癌的关联,以精确定位这些显著关联信号。
我们成功复制了 rs13385191(位于 C2orf43 基因,P=8.60×10(-5))、rs12653946(P=1.33×10(-6))、rs1983891(FOXP4,P=6.22×10(-5))和 rs339331(GPRC6A/RFX6,P=1.42×10(-5))与前列腺癌的关联。rs12653946 的最大比值比(OR)为 1.41(95%置信区间 1.18-1.68)。rs9600079 与本研究中的前列腺癌无显著关联(P=8.07×10(-2))。第二阶段研究进一步细化了这些关联信号,并确定了几个 SNP 与前列腺癌的关联比第一阶段测试的 SNP 更为显著。
我们的结果进一步支持了 C2orf43、FOXP4、GPRC6A 和 RFX6 基因与东亚人群前列腺癌的关联。本研究还更详细地描述了原始 GWAS 中报道的新基因座。还需要进一步的工作来确定功能变异,最终阐明潜在的生物学机制。