Xue Jianxin, Qin Zhiqiang, Li Xiao, Zhang Jianzhong, Zheng Yuxiao, Xu Weizhang, Cao Qiang, Wang Zengjun
Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Department of Urology, The Second Affiliated Hospital of Southeast University, Nanjing, 210003, China.
Oncotarget. 2017 Sep 8;8(46):80889-80899. doi: 10.18632/oncotarget.20720. eCollection 2017 Oct 6.
Recently, the functional polymorphisms in Cyclin D1 (CCND1) have been shown the potential influence to risk of renal cell cancer (RCC). Therefore, the present study was performed to investigate whether these polymorphisms could influence the susceptibility of RCC. Four potentially functional polymorphisms in CCND1 (rs1944129, rs7177, rs9344 and rs678653) were genotyped in this hospital-based case-control study, comprising of 1,488 RCC patients and 1,677 cancer-free controls in a Chinese population by the TaqMan assay. The logistic regression was used to assess the associations between CCND1 polymorphisms and the risk of RCC. We found the genotype and allele frequency distribution of rs1944129 and rs7177 were significantly associated with risk of RCC ( = 0.015 and = 0.018, respectively). The analysis of combined risk alleles revealed that patients with 2-4 risk alleles showed an elevated risk of RCC compared to those with 0-1 risk alleles (OR = 1.35, 95% CI = 1.15 - 1.58, < 0.001). Furthermore, compared with the genotypes containing G allele (AG and GG), the patients carrying the AA genotype in CCND1 rs1944129 polymorphism had a significantly greater prevalence of high clinical stage disease (OR = 0.56, 95% CI = 0.33 - 0.94, = 0.029). These results suggested that these CCND1 polymorphisms rs1944129 and rs7177 might contribute to the susceptibility of RCC in the Chinese population.
最近,细胞周期蛋白D1(CCND1)中的功能多态性已显示出对肾细胞癌(RCC)风险的潜在影响。因此,本研究旨在调查这些多态性是否会影响RCC的易感性。在这项基于医院的病例对照研究中,通过TaqMan分析对CCND1中的四个潜在功能多态性(rs1944129、rs7177、rs9344和rs678653)进行了基因分型,该研究纳入了1488例RCC患者和1677例中国人群中的无癌对照。采用逻辑回归分析评估CCND1多态性与RCC风险之间的关联。我们发现rs1944129和rs7177的基因型和等位基因频率分布与RCC风险显著相关(分别为 = 0.015和 = 0.018)。联合风险等位基因分析显示,与具有0 - 1个风险等位基因的患者相比,具有2 - 4个风险等位基因的患者患RCC的风险升高(OR = 1.35,95% CI = 1.15 - 1.58, < 0.001)。此外,与含有G等位基因的基因型(AG和GG)相比,CCND1 rs1944129多态性中携带AA基因型的患者高临床分期疾病的患病率显著更高(OR = 0.56,95% CI = 0.33 - 0.94, = 0.029)。这些结果表明,这些CCND1多态性rs1944129和rs7177可能与中国人群中RCC的易感性有关。