Xinjiang Medical University, Department of thoracic surgery, Feicheng Hospital Affiliated to Shandong First Medical University, China.
Department of Plastic Surgery, Feicheng Hospital Affiliated to Shandong First Medical University, China.
Medicine (Baltimore). 2022 Aug 19;101(33):e29253. doi: 10.1097/MD.0000000000029253.
Adenocarcinoma is the most common pathological type of lung cancer. The E2F7 transcription factor has been confirmed to be related to the occurrence and development of a variety of solid tumors, but the relationship with the prognosis of lung cancer is still unclear. Therefore, we conducted this study to explore the prognostic value of E2F7 for lung adenocarcinoma (LUAD) patients. In this study, we analyzed samples from the Cancer Genome Atlas (TCGA) to study the correlation between the expression of E2F7 and clinical features, the difference in expression between tumors and normal tissues, the prognostic and diagnostic value, and Enrichment analysis of related genes. All statistical analysis uses R statistical software (version 3.6.3). The result shows that the expression level of E2F7 in LUAD was significantly higher than that of normal lung tissue (P = 1e-34). High expression of E2F7 was significantly correlated with gender (P = .034), pathologic stage (P = .046) and M stage (P = .025). Multivariate Cox analysis confirmed that E2F7 is an independent risk factor for OS in LUAD patients (P = .027). Genes related to cell cycle checkpoints, DNA damage telomere stress-induced senescence, DNA methylation, chromosome maintenance and mitotic prophase showed differential enrichment in the E2F7 high expression group. In short, high expression of E2F7 is an independent risk factor for OS in LUAD patients and has a high diagnostic value.
腺癌是肺癌最常见的病理类型。E2F7 转录因子已被证实与多种实体瘤的发生发展有关,但与肺癌预后的关系尚不清楚。因此,我们进行了这项研究,旨在探讨 E2F7 对肺腺癌(LUAD)患者的预后价值。在本研究中,我们分析了癌症基因组图谱(TCGA)中的样本,以研究 E2F7 的表达与临床特征的相关性、肿瘤与正常组织之间的表达差异、预后和诊断价值以及相关基因的富集分析。所有统计分析均使用 R 统计软件(版本 3.6.3)。结果表明,LUAD 中 E2F7 的表达水平明显高于正常肺组织(P = 1e-34)。E2F7 的高表达与性别(P =.034)、病理分期(P =.046)和 M 分期(P =.025)显著相关。多因素 Cox 分析证实 E2F7 是 LUAD 患者 OS 的独立危险因素(P =.027)。与细胞周期检查点、DNA 损伤端粒应激诱导衰老、DNA 甲基化、染色体维持和有丝分裂前期相关的基因在 E2F7 高表达组中表现出差异富集。总之,E2F7 的高表达是 LUAD 患者 OS 的独立危险因素,具有较高的诊断价值。