An Peng, Wang Junhong, Fan Rong
Material Evidence Technology Center, School of Law, Tianjin University of Commerce, Tianjin, 300134, China.
School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China.
Sci Rep. 2025 Apr 11;15(1):12515. doi: 10.1038/s41598-025-97629-5.
Pancreatic ductal adenocarcinoma (PDAC) is a prevalent cancer with a high mortality rate. This study aims to identify and validate biomarkers for early PDAC diagnosis. We employed the GEO2R online tool to screen differentially expressed genes (DEGs), construct protein interaction networks, and perform functional enrichment analysis, survival prognosis analysis, and expression level validation. We identified 260 DEGs, comprising 165 upregulated genes and 95 downregulated genes. Following functional enrichment and survival analysis, we selected plasminogen activator urokinase (PLAU) for the RNA and protein level verification and preliminary cell phenotype analysis. We found that PLAU knockdown inhibits the proliferation and survival of pancreatic cancer cells. Therefore, PLAU may serve as a potential biomarker, offering new strategies for understanding PDAC's pathological mechanisms.
胰腺导管腺癌(PDAC)是一种常见且死亡率高的癌症。本研究旨在识别和验证用于早期PDAC诊断的生物标志物。我们使用GEO2R在线工具筛选差异表达基因(DEG)、构建蛋白质相互作用网络,并进行功能富集分析、生存预后分析和表达水平验证。我们鉴定出260个DEG,包括165个上调基因和95个下调基因。经过功能富集和生存分析后,我们选择尿激酶型纤溶酶原激活剂(PLAU)进行RNA和蛋白质水平验证以及初步细胞表型分析。我们发现敲低PLAU可抑制胰腺癌细胞的增殖和存活。因此,PLAU可能作为一种潜在的生物标志物,为理解PDAC的病理机制提供新策略。