Li Peng, Liu Hong-Liang, Zhang Zhi-Qiang, Lv Xiao-Dong, Chang Yu-Xi, Wang Hui-Juan, Ma Jie, Ma Zhi-Yong, Qu Xiu-Juan, Teng Yue-E
Department of Medical Oncology, The First Hospital of China Medical University, Shenyang 110001, China.
Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, The First Hospital of China Medical University, Shenyang 110001, China.
J Thorac Dis. 2018 Mar;10(3):1635-1647. doi: 10.21037/jtd.2018.02.31.
Casitas B-lineage lymphoma proto-oncogene-b (CBLB) influences the threshold of T cell activation and controlling peripheral T cell tolerance. In the present study, we hypothesize that potentially functional single nucleotide polymorphisms (SNPs) in CBLB are associated with clinical outcomes in patients advanced non-small cell lung cancer (NSCLC) treated with the first-line chemotherapy.
We genotyped three SNPs (rs2305035, rs3772534 and rs9657904) at CBLB in 116 advanced NSCLC patients with progression free survival (PFS) data and 133 advanced NSCLC patients with overall survival (OS) data, and we assessed their associations, 95% confidence interval (CI), with clinical outcomes by using Cox proportional hazards regression analyses. In silico functional analysis was also performed for the SNPs under investigation.
We found that associations between the three SNPs and PFS/OS were not significant in the overall NSCLC patients. The rs2305035 AA genotype was associated with a worse PFS in female patients and those of non-smokers or light smokers (95% CI, 1.14-11.81, P=0.030; 95% CI, 1.42-10.24, P=0.008; and 95% CI, 1.39-9.93, P=0.009; respectively), compared with the GG+AA genotypes. We also found that the rs9657904 CC genotype was significantly associated with a worse OS than TT + TC genotypes in male advanced NSCLC patients. Further in silico functional analysis revealed that the rs965704 T allele was significantly associated with lower mRNA expression levels of the CBLB gene.
Our findings identified two CBLB SNPs (rs2305035 and rs9657904) that were significantly associated with PFS and OS in several subgroups of Chinese advanced NSCLC patients after the first-line chemotherapy.
卡斯他斯B系淋巴瘤原癌基因b(CBLB)影响T细胞激活阈值并控制外周T细胞耐受性。在本研究中,我们假设CBLB中潜在的功能性单核苷酸多态性(SNP)与接受一线化疗的晚期非小细胞肺癌(NSCLC)患者的临床结局相关。
我们对116例有无进展生存期(PFS)数据的晚期NSCLC患者和133例有总生存期(OS)数据的晚期NSCLC患者的CBLB基因中的三个SNP(rs2305035、rs3772534和rs9657904)进行基因分型,并通过Cox比例风险回归分析评估它们与临床结局的关联及95%置信区间(CI)。还对所研究的SNP进行了计算机功能分析。
我们发现这三个SNP与总体NSCLC患者的PFS/OS之间的关联不显著。与GG+AA基因型相比,rs2305035的AA基因型在女性患者以及非吸烟者或轻度吸烟者中与较差的PFS相关(分别为95%CI,1.14 - 11.81,P = 0.030;95%CI,1.42 - 10.24,P = 0.008;95%CI,1.39 - 9.93,P = 0.009)。我们还发现,在男性晚期NSCLC患者中,rs9657904的CC基因型与比TT + TC基因型更差的OS显著相关。进一步的计算机功能分析显示,rs965704的T等位基因与CBLB基因较低的mRNA表达水平显著相关。
我们的研究结果确定了两个CBLB SNP(rs2305035和rs9657904),它们与中国晚期NSCLC患者一线化疗后的几个亚组中的PFS和OS显著相关。