中国临床解剖学杂志 ›› 2024, Vol. 42 ›› Issue (4): 448-452.doi: 10.13418/j.issn.1001-165x.2024.4.15

• 实验研究 • 上一篇    下一篇

COL4A1在胆管癌中的表达分析

唐婷1, 石玉莲2, 刘艳玲1, 李梅莲1, 戴景兴2*, 樊庭宇2*   

  1. 1. 中山大学肿瘤防治中心,  广州   510060; 2.南方医科大学解剖学教研室,  广州   510515
  • 收稿日期:2024-02-29 出版日期:2024-07-25 发布日期:2024-08-27
  • 作者简介:唐婷(1990-),女,湖南娄底人,护理师,研究方向为胆管癌的发生发展机制,E-mail:503187967@qq.com
  • 基金资助:
    国家重点研发计划项目(2022YFF1202603)

Analysis of COL4A1 expression in cholangiocarcinoma

Tang Ting1, Shi Yulian2, Liu Yanling1, Li Meilian1, Dai Jingxing2*, Fan Tingyu2*   

  1. 1.Sun Yat-Sen University Cancer Center, Guangzhou 510060, China; 2. Department of Anatomy, Southern Medical University, Guangzhou 510515, China  
  • Received:2024-02-29 Online:2024-07-25 Published:2024-08-27

摘要: 目的 探究胆管癌发生发展的分子机制。  方法 在GEO数据库中下载数据集GSE89749,并依次进行差异基因分析、GO/KEGG富集分析和蛋白-蛋白网络(PPI)分析以得到关键基因。TCGA数据库中分析COL4A1在肾上腺皮质癌、膀胱尿路上皮癌和乳腺浸润癌等16种癌症的基因表达情况。  结果 差异基因和GO/KEGG富集分析显示差异基因被显著富集在含胶原蛋白的细胞外基质。PPI分析结果显示基因胶原IVα1基因(COL4A1)为关键基因。COL4A1基因在胆管癌、结直肠癌和食管癌等8种癌症中高表达。  结论 COL4A1在胆管癌组织中显著高表达,这为探究胆管癌发生发展的分子机制提供了新的角度和实验基础。

关键词: 胆管癌,  GEO数据库,  TCGA数据库,  COL4A1

Abstract: Objective    To explore the molecular mechanisms underlying the development of cholangiocarcinoma.  Methods  The dataset GSE89749 was downloaded from the GEO database, and differential gene analysis, GO/KEGG enrichment analysis, and protein-protein interaction (PPI) analysis were sequentially performed to identify key genes. The expressions of COL4A1 in 16 types of cancers, including adrenocortical carcinoma, bladder urothelial carcinoma, and invasive breast carcinoma, were analyzed in the TCGA database.   Results    Differential gene and GO/KEGG enrichment analysis showed that differential genes were significantly enriched in the extracellular matrix containing collagen. PPI analysis identified the gene COL4A1 as a key gene. COL4A1 was found to be highly expressed in cholangiocarcinoma, colorectal cancer, and esophageal cancer among 8 types of cancers.   Conclusions   COL4A1 is significantly over-expressed in cholangiocarcinoma tissues, providing new perspective and experimental basis for exploring the molecular mechanisms of cholangiocarcinoma development.

Key words: Cholangiocarcinoma,  ,  , GEO database,  ,  , TCGA database,  ,  , COL4A1

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