Department of Clinical Biobank, Nantong University Affiliated Hospital, Nantong, P.R. China.
Department of Medicine, Nantong University Xinling College, Nantong, P.R. China.
Cancer Med. 2021 May;10(10):3403-3412. doi: 10.1002/cam4.3877. Epub 2021 May 2.
A primary factor in tumor morbidity and mortality, lung adenocarcinoma (LUAD) is known to be a major subtype of lung cancer, having the lowest survival rate among all other cancers. Using The Cancer Genome Atlas (TCGA) database the relationship between the immune infiltrate and the NUP62CL was explored and the value of the NUP62CL expression in the prognosis and diagnosis LUAD was examined. Using the logistic regression and the Wilcoxon signed-rank test the relationship between the NUP62CL and the clinico-pathological features was analyzed. There was a significant correlation between the clinical stage (p = 0.005), the N (p = 0.004), and the decreased expression of NUP62CL. The prognosis of LUAD with high NUP62CL expression was revealed to be worse than that with low NUP62CL expression (p < 0.001) by the Kaplan-Meier survival analysis. The potentiality of NUP62CL to be a significant factor of prognosis for LUAD was indicated by the analyses of the multivariate and the univariate Cox regression models. In LUAD, the crucial role of recombination and maintenance of telomere as a significant pathway for NUP62CL was suggested by the Gene Set Enrichment Analysis (GSEA). To analyze the correlation between the genes and the tumor infiltrating immune cells the CIBERSORT was used. Moreover the positive correlation with the NUP62CL expression in LUAD of the infiltration level of the tumor infiltrating B lymphocytes and memory CD4+ T cells was exhibited by CIBERSORT. Therefore, NUP62CL may be a new valuable prognostic indicator for LUAD.
肿瘤发病率和死亡率的一个主要因素是肺腺癌(LUAD),它是肺癌的主要亚型之一,在所有其他癌症中存活率最低。本研究利用癌症基因组图谱(TCGA)数据库探讨了免疫浸润与 NUP62CL 之间的关系,并研究了 NUP62CL 表达在 LUAD 预后和诊断中的价值。通过逻辑回归和 Wilcoxon 符号秩检验分析了 NUP62CL 与临床病理特征之间的关系。NUP62CL 与临床分期(p=0.005)、N 分期(p=0.004)呈负相关,且表达降低。通过 Kaplan-Meier 生存分析发现,NUP62CL 高表达的 LUAD 患者的预后比 NUP62CL 低表达的 LUAD 患者差(p<0.001)。多变量和单变量 Cox 回归模型分析表明,NUP62CL 具有 LUAD 预后的显著预测潜力。基因集富集分析(GSEA)表明,NUP62CL 在 LUAD 中作为一种重要的端粒重组和维持途径发挥关键作用。为了分析基因与肿瘤浸润免疫细胞之间的相关性,采用了 CIBERSORT 方法。此外,CIBERSORT 还显示,在 LUAD 中,NUP62CL 表达与肿瘤浸润性 B 淋巴细胞和记忆 CD4+T 细胞的浸润水平呈正相关。因此,NUP62CL 可能是 LUAD 的一个新的有价值的预后指标。