Department of Medical Oncology, The Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan 570311, China.
Department of Nursing, The Second Affiliated Hospital of Hainan Medical University, Haikou, Hainan 570311, China.
Biomed Res Int. 2018 Dec 24;2018:8305745. doi: 10.1155/2018/8305745. eCollection 2018.
Lung carcinoma is the most common cancer and cause of cancer deaths among both males and females in China. Previously, genetic variants located in gene untranslated region have been well established as interfering factors in mRNA translation and confirmed playing critical roles in lung oncogenesis. However, the correlation between polymorphisms in gene 3' untranslated region and lung cancer risk is less reported in China Han population. In this study, polymorphisms in 3'-untranslated region of , , and were determined in 322 lung cancer patients and 384 healthy controls with the usage of Sequenom MassARRAY. The correlation between selected variants and lung cancer risk was examined by unconditional logistic regression analysis with or without adjustments for age, gender, smoking status, and alcohol drinking status. Additionally, stratification analysis was applied to detect the associations of SNPs with lung cancer in different subgroups. As the results, significant relationships were found between rs859 and lung cancer susceptibility in recessive model (OR= 0.65, 95% CI: 0.44-0.96, = 0.029) and log-additive model (OR= 0.76, 95% CI: 0.60-0.96, = 0.019). Moreover, adjusted stratified analysis also revealed the important effects of rs859 on lung cancer risk among individuals aged older than 50, males, and nondrinkers. rs859 showed statistically significant evidence associated with susceptibility to lung adenocarcinoma and lung small cell carcinoma in Chinese Han population as well. Our research demonstrated that genetic variant rs859 of 3'UTR was associated with lung cancer risk in Chinese Han population and the result might be exploited as a new biomarker for lung cancer assessment and prevention.
肺癌是中国男性和女性中最常见的癌症和癌症死亡原因。先前,位于基因非翻译区的遗传变异已被证实是干扰 mRNA 翻译的因素,并被确认在肺癌发生中起关键作用。然而,在中国汉族人群中,基因 3'UTR 多态性与肺癌风险的相关性报道较少。在这项研究中,使用Sequenom MassARRAY 技术,在 322 名肺癌患者和 384 名健康对照中确定了 、 和 基因 3'UTR 中的多态性。通过无条件逻辑回归分析,在不调整或调整年龄、性别、吸烟状况和饮酒状况的情况下,检查了选定变体与肺癌风险之间的相关性。此外,还进行了分层分析,以检测 SNP 与不同亚组肺癌的关联。结果表明,在隐性模型(OR=0.65,95%CI:0.44-0.96,=0.029)和对数相加模型(OR=0.76,95%CI:0.60-0.96,=0.019)中, rs859 与肺癌易感性之间存在显著关系。此外,调整后的分层分析还表明, rs859 对 50 岁以上、男性和非饮酒者的肺癌风险有重要影响。 rs859 在中国汉族人群中也与肺腺癌和肺小细胞癌的易感性有统计学意义的关联。我们的研究表明, 基因 3'UTR 的遗传变异 rs859 与中国汉族人群的肺癌风险相关,该结果可能被用作肺癌评估和预防的新生物标志物。