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Polymorphisms in the PVT1 Gene and Susceptibility to the Lung Cancer in a Chinese Northeast Population: a Case-control Study

机译:PVT1基因中的多态性和中国东北人群中肺癌的易感性:一个病例对照研究

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Background: Long non-coding RNA (lncRNA) PVT1 has been identified to be related to risk of a variety of cancers, such as gastric cancer, pancreatic cancer and follicular lymphoma. This study assesses the association between genetic polymorphisms of PVT1 and the susceptibility to lung cancer as well as gene-environmental interaction. Method: A hospital-based case-control study, including 515 lung cancer patients and 582 healthy controls, was carried out in Shenyang, China. Unconditional logistic regression analyses calculated the odds ratios (ORs) and their 95% confidence intervals (CIs) to assess the associations between polymorphisms of rs2608053, rs1561927, rs13254990 and susceptibility to lung cancer. The gene-environment interaction was evaluated by additive model and multiplicative model. Results: There were no statistically significant associations between rs2608053 and rs1561927 polymorphisms in PVT1 and risk of lung cancer in the overall population. The relationship between polymorphism rs13254990 in PVT1 gene and lung adenocarcinoma was significant. Composed with individuals carrying CC genotypes, TT genotype carriers were more likely to develop lung adenocarcinoma (adjusted OR=2.095; 95%CI=1.084-4.047, P=0.028). In the recessive model, it also showed a statistically significant difference (TT vs CT CC: adjusted OR=2.251, 95%CI=1.174-4.318, P=0.015). In nonsmokers, individuals carrying genotype CT had a lower risk of lung cancer than those with CC genotype (adjusted OR=0.673, 95%CI=0.472-0.959, P=0.028). Comparing with the homozygous CC, the patients with the heterozygous CT had a lower risk of NCSLC in the non-smoking group (adjusted OR =0.685, 95%CI=0.477-0.984, P=0.040). Additionally, gene-environment interaction results were not statistically significant in either additive model or multiplicative model. Conclusion: The polymorphism rs13254990 in PVT1 gene is associated with the risk of lung adenocarcinoma in a Chinese northeast population.? The author(s).
机译:背景:已经鉴定了长期非编码RNA(LNCRNA)PVT1与各种癌症的风险有关,例如胃癌,胰腺癌和滤泡淋巴瘤。本研究评估PVT1遗传多态性与肺癌的敏感性以及基因 - 环境相互作用的关联。方法:中国沉阳,包括515名肺癌患者和582名健康对照,包括515名肺癌患者的病例对照研究。无条件逻辑回归分析计算了几率比(OR)及其95%的置信区间(CIS),以评估RS2608053,RS1561927,RS13254990的多态性之间的关联和对肺癌的易感性。通过添加模型和乘法模型评估基因环境相互作用。结果:PVT1的RS2608053和RS1561927多态性之间没有统计上显着的关联,以及整体人群中肺癌的风险。 PVT1基因和肺腺癌中多态性Rs13254990的关系显着。与携带CC基因型的个体组成,TT基因型载体更可能发育肺腺癌(调节或= 2.095; 95%CI = 1.084-4.047,P = 0.028)。在隐性模型中,它还表现出统计学上显着的差异(TT VS CT CC:调整或= 2.251,95%CI = 1.174-4.318,P = 0.015)。在非莫克者中,携带基因型CT的个体具有肺癌风险较低的风险低于CC基因型(调节或= 0.673,95%CI = 0.472-0.959,P = 0.028)。与纯合酶CC相比,杂合CT的患者在非吸烟组中具有较低的NCSLC风险(调节或= 0.685,95%CI = 0.477-0.984,P = 0.040)。另外,在添加剂模型或乘法模型中,基因环境相互作用结果在统计学上没有统计学意义。结论:PVT1基因中的多态性RS13254990与中国东北人群肺腺癌的风险有关。作者。

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