Department of Thoracic Surgery, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China.
Research Center for Translational Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China.
Oxid Med Cell Longev. 2020 Dec 19;2020:8847226. doi: 10.1155/2020/8847226. eCollection 2020.
Lung adenocarcinoma (LUAD), a major and fatal subtype of lung cancer, caused lots of mortalities and showed different outcomes in prognosis. This study was to assess key genes and to develop a prognostic signature for the patient therapy with LUAD.
RNA expression profile and clinical data from 522 LUAD patients were accessed and downloaded from the Cancer Genome Atlas (TCGA) database. Differentially expressed genes (DEGs) were extracted and analyzed between normal tissues and LUAD samples. Then, a 14-DEG signature was developed and identified for the survival prediction in LUAD patients by means of univariate and multivariate Cox regression analyses. The gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were performed to predict the potential biological functions and pathways of these DEGs.
Twenty-two out of 5924 DEGs in the TCGA dataset were screened and associated with the overall survival (OS) of LUAD patients. 14CID="C008" value=" "DEGs were finally selected and included in our development and validation model by risk score analysis. The ROC analysis indicated that the specificity and sensitivity of this profile signature were high. Further functional enrichment analyses indicated that these DEGs might regulate genes that affect the function of release of sequestered calcium ion into cytosol and pathways that associated with vibrio cholerae infection.
Our study developed a novel 14-DEG signature providing more efficient and persuasive prognostic information beyond conventional clinicopathological factors for survival prediction of LUAD patients.
肺腺癌(LUAD)是肺癌的一个主要且致命的亚型,导致了大量的死亡,并在预后方面表现出不同的结果。本研究旨在评估关键基因,并为 LUAD 患者的治疗开发一个预后特征。
从癌症基因组图谱(TCGA)数据库中获取并下载了 522 例 LUAD 患者的 RNA 表达谱和临床数据。在正常组织和 LUAD 样本之间提取和分析差异表达基因(DEGs)。然后,通过单变量和多变量 Cox 回归分析,为 LUAD 患者的生存预测开发和鉴定了一个 14-DEG 特征。进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路富集分析,以预测这些 DEGs 的潜在生物学功能和途径。
在 TCGA 数据集的 5924 个 DEGs 中筛选出 22 个与 LUAD 患者的总生存期(OS)相关。通过风险评分分析,最终选择了 14 个 CID="C008" value=" "DEGs 并将其纳入我们的开发和验证模型。ROC 分析表明该特征谱具有较高的特异性和敏感性。进一步的功能富集分析表明,这些 DEGs 可能调节影响细胞质中钙离子释放功能的基因,以及与霍乱弧菌感染相关的途径。
本研究开发了一个新的 14-DEG 特征,为 LUAD 患者的生存预测提供了比传统临床病理因素更有效和有说服力的预后信息。