Li Xiaoqian
Department of Stomatology, Tianjin First Central Hospital, Nankai District, Tianjin, P.R. China.
Int Dent J. 2025 Apr;75(2):1165-1175. doi: 10.1016/j.identj.2024.07.012. Epub 2024 Aug 15.
Oral squamous cell carcinoma (OSCC) is the most common type of malignant tumour in the oral cavity, and it is known for its poor prognosis. Budding uninhibited by benzimidazoles 1 (BUB1) may be related to cancer prognosis; however, the specific relationship between BUB1 and OSCC prognosis remains largely unexplored.
The mRNA levels of BUB1 were analysed using data from the TCGA_OSCC and GSE23558 cohorts. OSCC samples from the TCGA_OSCC dataset were divided into low- and high-BUB1 expression groups based on the median BUB1 level. Furthermore, results of survival analysis, tumour mutation burden (TMB), gene set enrichment analysis (GSEA) pathways, and drug-sensitivity analysis were compared between the 2 groups.
Based on the data from the TCGA_OSCC and GSE23558 cohorts, BUB1 mRNA levels were significantly upregulated in OSCC tissues compared to healthy controls. Moreover, high expression of BUB1 may serve as an independent indicator of poor prognosis in OSCC. Additionally, patients with high BUB1 expression also exhibited increased levels of immune checkpoints and TMB, suggesting that patients with high BUB1 expression may benefit from immunotherapy. Mechanistically, transcription factors ZFP64, TCF3, and ZNF281 were found to potentially bind to the promoter region of BUB1, thereby regulating its gene expression. Furthermore, GSEA results showed that BUB1 expression was closely related to cell cycle and tumour-related pathways in OSCC. Drug-sensitivity analysis showed that patients with high BUB1 expression may be more sensitive to gemcitabine, paclitaxel, or imatinib.
Collectively, results demonstrated that high BUB1 levels may be related to a poor prognosis of OSCC, highlighting its potential as a novel prognostic biomarker for OSCC.
口腔鳞状细胞癌(OSCC)是口腔中最常见的恶性肿瘤类型,其预后较差。苯并咪唑不抑制的芽殖蛋白1(BUB1)可能与癌症预后相关;然而,BUB1与OSCC预后之间的具体关系在很大程度上仍未得到探索。
使用来自TCGA_OSCC和GSE23558队列的数据来分析BUB1的mRNA水平。基于TCGA_OSCC数据集中BUB1的中位数水平,将OSCC样本分为低BUB1表达组和高BUB1表达组。此外,比较了两组之间的生存分析结果、肿瘤突变负担(TMB)、基因集富集分析(GSEA)途径和药物敏感性分析结果。
基于TCGA_OSCC和GSE23558队列的数据,与健康对照相比,OSCC组织中BUB1的mRNA水平显著上调。此外,BUB1的高表达可能是OSCC预后不良的独立指标。此外,BUB1表达高的患者还表现出免疫检查点和TMB水平升高,这表明BUB1表达高的患者可能从免疫治疗中获益。从机制上讲,发现转录因子ZFP64、TCF3和ZNF281可能与BUB1的启动子区域结合,从而调节其基因表达。此外,GSEA结果表明,BUB1表达与OSCC中的细胞周期和肿瘤相关途径密切相关。药物敏感性分析表明,BUB1表达高的患者可能对吉西他滨、紫杉醇或伊马替尼更敏感。
总体而言,结果表明BUB1水平高可能与OSCC的不良预后相关,突出了其作为OSCC新型预后生物标志物的潜力。