Zhu Xiaonian, Wang Zhigang, Qiu Xiaoqiang, Tan Chao, Yu Hongping, Bei Chunhua, Qin Linyuan, Ren Yuan, Tan Shengkui
Department of Epidemiology, School of Public Health, Guilin Medical University, Guilin 541004, Guangxi, People's Republic of China and.
Department of Epidemiology, School of Public Health, Guangxi Medical University, Nanning 530021, Guangxi, People's Republic of China.
Carcinogenesis. 2017 May 1;38(5):532-540. doi: 10.1093/carcin/bgx031.
Down-regulated RINGl and YYl binding protein (RYBP) is reported to be an independent predictor of a poor prognosis in patients with hepatocellular carcinoma (HCC). However, the genetic association of RYBP polymorphisms with HCC risk and prognosis has not been investigated now. In this study, five RYBP SNPs, rs12956, rs2118593, rs17009699, rs4676875 and rs4532099, were studied from a hospital-based case-control study including 1100 cases (HCC patients) and 1100 controls (non-HCC patients) in Guangxi, China. All these SNPs interacted with environmental risk factors, such as HBV infection, alcohol intake and smoking in the pathogenesis of HCC. Compared to the CC genotype, patients with TT genotype of rs12956 had a decreased risk of HCC (OR = 0.587, 95% CI = 0.4030.923) and an increased survival time (Co-dominant, HR = 0.745, 95% CI = 0.5940.934), while those with TT genotype of rs2118593 had an increased risk of HCC (OR = 1.538, 95% CI = 1.0932.735) and a decreased survival time (Co-dominant, HR = 1.447, 95% CI = 1.1741.782). No significant difference was found between the other three RYBP polymorphisms with HCC risk and prognosis. Furthermore, we found that tumor number, tumor staging, metastasis and rs2118593 were associated with the overall survival of HCC patients by multivariate COX regression analysis. Our study suggests RYBP SNP, rs2118593 as a new predictor for poor prognosis of HCC patients.
据报道,下调的RING1和YY1结合蛋白(RYBP)是肝细胞癌(HCC)患者预后不良的独立预测指标。然而,目前尚未研究RYBP基因多态性与HCC风险及预后的遗传关联。在本研究中,我们从中国广西一项基于医院的病例对照研究中选取了5个RYBP单核苷酸多态性(SNP),即rs12956、rs2118593、rs17009699、rs4676875和rs4532099,该研究包括1100例病例(HCC患者)和1100例对照(非HCC患者)。所有这些SNP在HCC发病机制中均与环境危险因素相互作用,如乙肝病毒感染、饮酒和吸烟。与CC基因型相比,rs12956的TT基因型患者HCC风险降低(OR = 0.587,95%CI = 0.4030.923)且生存时间延长(共显性,HR = 0.745,95%CI = 0.5940.934),而rs2118593的TT基因型患者HCC风险增加(OR = 1.538,95%CI = 1.0932.735)且生存时间缩短(共显性,HR = 1.447,95%CI = 1.1741.782)。另外三个RYBP多态性与HCC风险及预后之间未发现显著差异。此外,通过多因素COX回归分析,我们发现肿瘤数量、肿瘤分期、转移和rs2118593与HCC患者的总生存相关。我们的研究表明,RYBP SNP rs2118593是HCC患者预后不良的一个新的预测指标。