Yan Shouchun, Wu Shouzhen, Wu Jia, Zhang Qinlu, He Yongjun, Jiang Chao, Jin Tianbo
Department of Emergency Medicine, The Second Affiliated Hospital of Shaanxi University of Chinese Medicine, Xianyang 712000, Shaanxi Province, China.
School of Nursing, Shaanxi University of Chinese Medicine, Xianyang 712046, Shaanxi Province, China.
Open Med (Wars). 2023 Mar 9;18(1):20230655. doi: 10.1515/med-2023-0655. eCollection 2023.
Lung cancer is one of the malignant tumors, and genetic background is a risk factor in lung cancer that cannot be neglected. In this study, we aimed to find out the effect of MRPS30-DT and NINJ2 variants on lung cancer risk. In this study, the seven selected single-nucleotide polymorphisms (SNPs) of MRPS30-DT and NINJ2 were genotyped in 509 lung cancer patients and 501 healthy controls based on the Agena MassARRAY platform. Odds ratios and 95% confidence intervals were calculated by logistic regression analysis to evaluate association between gene polymorphisms and lung cancer risk. False-positive report probability was also used to assess false-positive results. Furthermore, the interaction between SNPs was analyzed by multifactor dimensionality reduction to predict lung cancer risk. We identified the genotype TA of rs16901963 (T < A) in MRPS30-DT as a protective factor against lung cancer, while rs16901963-TT was significantly associated with an increased risk of lung cancer. We also revealed that the effect of MRPS30-DT and NINJ2 variants on the risk of lung cancer was dependent on age, gender, smoking, and drinking status. In conclusion, this study first proved that MRPS30-DT and NINJ2 variants played important roles in affecting the susceptibility to lung cancer.
肺癌是恶性肿瘤之一,遗传背景是肺癌中一个不可忽视的风险因素。在本研究中,我们旨在探究MRPS30-DT和NINJ2基因变异对肺癌风险的影响。在本研究中,基于Agena MassARRAY平台,对509例肺癌患者和501例健康对照者进行了MRPS30-DT和NINJ2的7个选定单核苷酸多态性(SNP)的基因分型。通过逻辑回归分析计算优势比和95%置信区间,以评估基因多态性与肺癌风险之间的关联。还使用假阳性报告概率来评估假阳性结果。此外,通过多因素降维分析SNP之间的相互作用,以预测肺癌风险。我们确定MRPS30-DT中rs16901963(T < A)的基因型TA是肺癌的一个保护因素,而rs16901963-TT与肺癌风险增加显著相关。我们还发现,MRPS30-DT和NINJ2基因变异对肺癌风险的影响取决于年龄、性别、吸烟和饮酒状况。总之,本研究首次证明MRPS30-DT和NINJ2基因变异在影响肺癌易感性方面发挥重要作用。