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Genetic score of multiple risk-associated single nucleotide polymorphisms is a marker for genetic susceptibility to bladder cancer

机译:多个与风险相关的单核苷酸多态性的遗传评分是膀胱癌遗传易感性的标志

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Genome-wide association studies have identified 13 single nucleotide polymorphisms (SNPs) that are associated with bladder cancer; three of these SNPs were validated in the Chinese population. This study assessed the performance of these three SNPs, in combination, to predict genetic susceptibility to bladder cancer in Chinese. Three previously established bladder cancer risk-associated SNPs (rs798766 in TACC3, rs9642880 in MYC, and rs2294008 in PSCA) were genotyped in 1,210 bladder cancer patients and 1,008 control subjects in Shanghai, China. A genetic score was calculated for each subject based on these three SNPs. Each of these three SNPs was significantly associated with bladder cancer risk in this independent study population, P < 0.05. The genetic score based on these three SNPs was significantly higher in cases than controls, with a mean of 1.05 and 0.99, respectively, P = 1.03E-05. Compared with subjects with a genetic score <= 1.00, subjects with an elevated genetic score (>1.00) had a significantly increased risk for bladder cancer after adjusting for age, gender, and smoking status, OR = 1.58, 95% Confidence Interval (CI) = 1.21 - 2.06, P = 0.0007. When tested separately for lower (Ta) or higher (Tis, T1-T4) tumor stage, the association was significantly stronger for lower (OR = 2.24, 95% CI = 1.66 - 3.01, P = 1.02E-07) than higher tumor stage (OR = 1.33, 95% CI = 1.00 - 1.78, P = 0.05), P = 0.001. In conclusion, A combination of three previously implicated bladder cancer risk-associated SNPs is a significant predictor of genetic susceptibility to bladder cancer in Chinese.
机译:全基因组关联研究已经确定了13种与膀胱癌相关的单核苷酸多态性(SNP)。这些SNP中的三个已在中国人群中得到验证。这项研究评估了这三个SNP的综合性能,以预测中国人对膀胱癌的遗传易感性。在中国上海的1,210名膀胱癌患者和1,008名对照受试者中,对三个先前建立的与膀胱癌风险相关的SNP(TACC3中的rs798766,MYC中的rs9642880和PSCA中的rs2294008)进行了基因分型。基于这三个SNP,为每个受试者计算遗传评分。在该独立研究人群中,这三个SNP中的每一个均与膀胱癌风险显着相关,P <0.05。在这三种情况下,基于这三个SNP的遗传评分显着高于对照组,平均值分别为1.05和0.99,P = 1.03E-05。与遗传评分<= 1.00的受试者相比,遗传评分升高(> 1.00)的受试者在调整了年龄,性别和吸烟状况后,患膀胱癌的风险显着增加,OR = 1.58,95%的置信区间(CI) )= 1.21-2.06,P = 0.0007。当分别测试较低(Ta)或较高(Tis,T1-T4)肿瘤分期时,与较低肿瘤(OR = 2.24,95%CI = 1.66-3.01,P = 1.02E-07)的关联明显更强。阶段(OR = 1.33,95%CI = 1.00-1.78,P = 0.05),P = 0.001。总之,三个先前与膀胱癌风险相关的SNP的组合是中国人对膀胱癌遗传易感性的重要预测指标。

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