Department of Thoracic Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi.
Department of Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
Eur J Cancer Prev. 2022 Jan 1;31(1):7-13. doi: 10.1097/CEJ.0000000000000671.
FCGR2A, ORAI1 and CD40 are all involved in the immune and inflammatory responses in the human body, whereas its association with lung cancer is still unclear. This study aimed to investigate the effects of polymorphisms in these genes on the susceptibility to lung cancer. Six candidate single nucleotide polymorphisms (SNPs) were genotyped using a MassARRAY platform in a discovery cohort, including 400 lung cancer patients and 400 healthy controls, and validated in a replication cohort, including 529 lung cancer cases and 532 controls. Comparing the allele frequency distributions, we found that the rs1801274-G, rs511278-T and rs1883832-T were risk alleles for lung cancer (P < 0.05), whereas the minor allele of rs12320939-T was a protective allele for the disease (P = 0.037). Comparing the genotype frequency distributions, we found that rs1801274-GG, rs511278-CT and of rs1883832-TT were risk genotype for lung cancer (P < 0.05). Genetic model analysis showed that the rs1801274 A>G was correlated with an elevated risk of lung cancer in recessive and log-additive models (P < 0.05); rs511278 C>T exhibited an increased risk of disease in dominant and log-additive models (P < 0.05); rs1883832 C>T had a strong relationship with risk of disease in all three models (P < 0.001), whereas rs12320939 G>T was correlated to a reduced risk of disease in recessive and log-additive models (P < 0.05). Finally, the association between the above SNPs and lung cancer risk was validated in a replication cohort (P < 0.05). These results shed new light on the association between immune-related genes and risk of lung cancer, and might be useful for the identification of high-risk individuals.
FCGR2A、ORAI1 和 CD40 均参与人体的免疫和炎症反应,但其与肺癌的关系尚不清楚。本研究旨在探讨这些基因的多态性与肺癌易感性的关系。在一个发现队列中,使用 MassARRAY 平台对 6 个候选单核苷酸多态性(SNP)进行基因分型,包括 400 例肺癌患者和 400 例健康对照,在一个验证队列中,包括 529 例肺癌病例和 532 例对照,对其进行验证。比较等位基因频率分布,发现 rs1801274-G、rs511278-T 和 rs1883832-T 是肺癌的风险等位基因(P<0.05),而 rs12320939-T 的次要等位基因是疾病的保护等位基因(P=0.037)。比较基因型频率分布,发现 rs1801274-GG、rs511278-CT 和 rs1883832-TT 是肺癌的风险基因型(P<0.05)。遗传模型分析显示,rs1801274 A>G 在隐性和对数相加模型中与肺癌风险升高相关(P<0.05);rs511278 C>T 在显性和对数相加模型中显示出疾病风险增加(P<0.05);rs1883832 C>T 在所有三种模型中与疾病风险有很强的关系(P<0.001),而 rs12320939 G>T 在隐性和对数相加模型中与疾病风险降低相关(P<0.05)。最后,在一个验证队列中验证了上述 SNP 与肺癌风险的关系(P<0.05)。这些结果为免疫相关基因与肺癌风险之间的关系提供了新的认识,可能有助于识别高危个体。