医学分子生物学杂志 ›› 2025, Vol. 22 ›› Issue (5): 452-461.doi: 10.3870/j.issn.1672-8009.2025.05.006

• 论著 • 上一篇    下一篇

鉴定 EPDR1 作为胃癌预后的生物标志物及其对胃癌细胞侵袭迁移的影响 #br#

  

  1. 武汉大学中南医院1胃肠外科,2肿瘤生物学行为湖北省重点实验室 & 湖北省肿瘤医学临床研究中心 武汉市, 430071
  • 出版日期:2025-09-30 发布日期:2025-10-09

Identification of EPDR1 as Prognostic Biomarker of Gastric Cancer and Its Effect on Invasion and Migration of Gastric Cancer Cells #br#

  1. 1Department of Gastrointestinal Surgery,2Hubei Key Laboratory of Tumor Biological Behaviors and Hubei Cancer Clinical Study Center, Zhongnan Hospital of Wuhan University, Wuhan, 430071, China
  • Online:2025-09-30 Published:2025-10-09

摘要: 目的 分析室管膜蛋白相关蛋白 1 (ependymin related protein 1, EPDR1) 在胃癌 (gastric cancer,GC) 中表达水平及与 GC 患者预后的关系, 并进一步探究 EPDR1 GC 细胞侵袭迁移的影响及潜在机制方法 分析 TCGA-GTEx、 GEO 数据库中的 GSE62254 数据集中胃粘膜组织, 胃癌患者的胃癌组织及其癌旁组织中 EPDR1 表达水平及其与对应患者临床病理特征及预后的关系; 通过基因集富集分析 ( GSEA) 探索EPDR1 GC 中可能调控的信号通路; 通过 RT-qPCR、 蛋白质印迹免疫荧光以及 Transwell 实验探究EPDR1 GC 细胞迁移和侵袭的影响及潜在机制结果 生物信息学分析显示, EPDR1 GC 的原发灶及腹膜转移灶中均显著高表达, 且其高表达与 GC 患者较差的无病生存期和总生存期密切相关; GSEA 分析表明, EPDR1 可能通过激活 Wnt / β-catenin 信号通路参与 GC 的发生发展; 体外细胞实验表明, 过表达 EPDR1可增强 GC 细胞的迁移和侵袭能力, 同时可活化 Wnt / β-catenin 通路促进 CTNNB1 蛋白表达上调并向核内转位结论 EPDR1 GC 中高表达, 其与 GC 的侵袭迁移及不良预后密切相关, 可作为 GC 预后评估的生物标志物和潜在的治疗靶点

关键词: 胃癌, 室管膜蛋白相关蛋白 1, Wnt / β-catenin 通路, 预后, 生物信息学分析

Abstract: Objective To analyze the expression level of recombinant ependymin-related protein 1 (EPDR1) in gastric cancer ( GC) and its relationship with the prognosis of GC patients,and to further explore the effect of EPDR1 on the invasive and migrative abilities of GC cells and itspotential mechanism. Methods The expression levels of EPDR1 in gastric cancer tissues and adjacent non-cancerous tissues from the GSE62254 dataset of the GEO database and TCGA-GTEx were analyzed, and their associations with clinicopathological characteristics and prognosis of corresponding patients were investigated. Gene set enrichment analysis (GSEA) was used to explore the signaling pathways that EPDR1 might regulate in GC. The effects of EPDR1 on the migration and invasion of GC cells and its potential mechanism were investigated by RT-qPCR, Western blotting, immunofluorescence, and Transwell assay. Results Bioinformatics analysis showed that EPDR1 was significantly overexpressed in both the primary and peritoneal metastases of GC, and its high expression was closely related to poor disease-free survival and overall survival of GC patients. GSEA analysis indicated that EPDR1 may participate in the occurrence and development of GC by activating theWnt / β-catenin signaling pathway. In vitro cell experiments showed that overexpression of EPDR1 enhanced the migrative and invasive abilities of GC cells, and activated the Wnt / β-catenin pathway topromote the up-regulation of CTNNB1 protein and endonuclear translocation. Conclusion EPDR1is highly expressed in GC, which is closely related to the invasion, migration, and poor prognosis of GC, and can be used as a prognostic biomarker and potential therapeutic target for GC.

Key words:

gastric cancer, ependymin related protein 1, Wnt / β-catenin pathway, prognosis, bioinformatics analysis

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