Jinga Viorel, Csiki Irma Eva, Manolescu Andrei, Iordache Paul, Mates Ioan Nicolae, Radavoi Daniel, Rascu Stefan, Badescu Daniel, Badea Paula, Mates Dana
"Prof. Dr. Th. Burghele" Clinical Hospital, Urology Department, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
National Institute of Public Health, Bucharest, Romania.
J Cell Mol Med. 2016 Apr;20(4):594-600. doi: 10.1111/jcmm.12729. Epub 2016 Jan 15.
Prostate cancer is the third-most common form of cancer in men in Romania. The Romanian unscreened population represents a good sample to study common genetic risk variants. However, a comprehensive analysis has not been conducted yet. Here, we report our replication efforts in a Romanian population of 979 cases and 1027 controls, for potential association of 34 literature-reported single nucleotide polymorphisms (SNPs) with prostate cancer. We also examined whether any SNP was differentially associated with tumour grade or stage at diagnosis, with disease aggressiveness, and with the levels of PSA (prostate specific antigen). In the allelic analysis, we replicated the previously reported risk for 19 loci on 4q24, 6q25.3, 7p15.2, 8q24.21, 10q11.23, 10q26.13, 11p15.5, 11q13.2, 11q13.3. Statistically significant associations were replicated for other six SNPs only with a particular disease phenotype: low-grade tumour and low PSA levels (rs1512268), high PSA levels (rs401681 and rs11649743), less aggressive cancers (rs1465618, rs721048, rs17021918). The strongest association of our tested SNP's with PSA in controls was for rs2735839, with 29% increase for each copy of the major allele G, consistent with previous results. Our results suggest that rs4962416, previously associated only with prostate cancer, is also associated with PSA levels, with 12% increase for each copy of the minor allele C. The study enabled the replication of the effect for the majority of previously reported genetic variants in a set of clinically relevant prostate cancers. This is the first replication study on these loci, known to associate with prostate cancer, in a Romanian population.
前列腺癌是罗马尼亚男性中第三常见的癌症形式。罗马尼亚未接受筛查的人群是研究常见遗传风险变异的良好样本。然而,尚未进行全面分析。在此,我们报告了在罗马尼亚的979例病例和1027例对照人群中的重复研究结果,以探讨34个文献报道的单核苷酸多态性(SNP)与前列腺癌的潜在关联。我们还研究了是否有任何SNP与诊断时的肿瘤分级或分期、疾病侵袭性以及前列腺特异性抗原(PSA)水平存在差异关联。在等位基因分析中,我们重复了先前报道的4q24、6q25.3、7p15.2、8q24.21、10q11.23、10q26.13、11p15.5、11q13.2、11q13.3上19个位点的风险。仅在特定疾病表型中重复了其他六个SNP的统计学显著关联:低级别肿瘤和低PSA水平(rs1512268)、高PSA水平(rs401681和rs11649743)、侵袭性较低的癌症(rs1465618、rs721048、rs17021918)。在对照中,我们测试的SNP与PSA的最强关联是rs2735839,每个主要等位基因G拷贝增加29%,与先前结果一致。我们的结果表明,先前仅与前列腺癌相关的rs4962416也与PSA水平相关,每个次要等位基因C拷贝增加12%。该研究使得在一组临床相关的前列腺癌中重复了大多数先前报道的遗传变异的效应。这是在罗马尼亚人群中对这些已知与前列腺癌相关的位点进行的首次重复研究。