Zhang Yuxuan, Huang Qibing
Department of Emergency Neurosurgical Intensive Care Unit, Qilu Hospital of Shandong University, Jinan, 250012, People's Republic of China.
Int J Gen Med. 2025 Mar 31;18:1807-1821. doi: 10.2147/IJGM.S512624. eCollection 2025.
Cancer-associated fibroblasts (CAFs) could promote the progression and migration of tumors. However, the roles of CAFs infiltration related genes in glioblastoma (GBM) were still unclear.
GBM-related transcriptome data and clinical information were downloaded from the UCSC Xena and CGGA databases. In this study, the abundance of fibroblasts were calculated by "MCPcounter", and the CAFs infiltration related genes were identified by "WGCNA". Then, the biomarkers of GBM were screened out, and based on it, the survival risk model (risk score) and the prognostic model (nomogram) were constructed to clinical predict the survival of GBM. Moreover, the function and mutation analyses were performed to further study the mechanisms of GBM. Furthermore, the competitive endogenous RNAs (ceRNA) regulatory network were used to reveal the potential regulation of biomarkers.
Totals of 46 CAFs infiltration related genes were associated with focal adhesion. Four biomarkers, including STC1, BDKRB2, SOCS3 and FURIN were identified, and all of them were negative factors. Nomogram constructed based on risk scores and clinical indicators had good predictive performance (AUC > 0.68). Noticeable, COL5A1 might be the key gene, which were extremely positively associated with all these four biomarkers. Besides, the genes in high-risk groups were associated with the functions of epithelial mesenchymal transition (EMT) and angiogenesis. In addition, hsa-miR-107 could regulate STC1 through the TGF-β signaling pathway and further regulating the migration and invasion of tumour.
This study identified four CAFs infiltration related biomarkers associated with the prognosis of GBM. This finding might help to deepen the understanding the roles of CAFs in development of GBM.
癌症相关成纤维细胞(CAFs)可促进肿瘤进展和迁移。然而,CAFs浸润相关基因在胶质母细胞瘤(GBM)中的作用仍不清楚。
从UCSC Xena和CGGA数据库下载GBM相关转录组数据和临床信息。本研究中,通过“MCPcounter”计算成纤维细胞丰度,通过“WGCNA”鉴定CAFs浸润相关基因。然后,筛选出GBM的生物标志物,并在此基础上构建生存风险模型(风险评分)和预后模型(列线图)以临床预测GBM的生存情况。此外,进行功能和突变分析以进一步研究GBM的机制。此外,利用竞争性内源性RNA(ceRNA)调控网络揭示生物标志物的潜在调控作用。
共有46个CAFs浸润相关基因与粘着斑相关。鉴定出4个生物标志物,包括STC1、BDKRB2、SOCS3和FURIN,且均为负性因子。基于风险评分和临床指标构建的列线图具有良好的预测性能(AUC>0.68)。值得注意的是,COL5A1可能是关键基因,它与所有这4个生物标志物均呈极显著正相关。此外,高危组基因与上皮间质转化(EMT)和血管生成功能相关。此外,hsa-miR-107可通过TGF-β信号通路调控STC1,进而调节肿瘤的迁移和侵袭。
本研究鉴定出4个与GBM预后相关的CAFs浸润相关生物标志物。这一发现可能有助于加深对CAFs在GBM发生发展中作用的理解。