Department of General Dentistry, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, P.R. China.
Shanghai Key Laboratory of Stomatology and Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, 200000, P.R. China.
Biosci Rep. 2020 Jan 31;40(1). doi: 10.1042/BSR20193349.
DNA methylation has been demonstrated to play significant roles in the etiology and pathogenesis of head and neck squamous cell carcinoma (HNSCC). In the present study, methylation microarray dataset (GSE87053) and gene expression microarray dataset (GSE23558) were downloaded from GEO database and analyzed through R language. A total of 255 hypermethylated-downregulated genes and 114 hypomethylated-upregulated genes were finally identified. Functional enrichment analyses were performed and a comprehensive protein-protein interaction (PPI) network was constructed. Subsequently, the top ten hub genes selected by Cytoscape software were subjected to further analyses. It was illustrated that the expression level of CSF2, CTLA4, ETS1, PIK3CD, and CFTR was intimately associated with HNSCC. Survival analysis suggested that CTLA4 and FGFR2 could serve as effective independent prognostic biomarkers for HNSCC patients. Overall, our study lay a groundwork for further investigation into the underlying molecular mechanisms in HNSCC carcinogenesis, providing potential biomarkers and therapeutic targets for HNSCC.
DNA 甲基化已被证明在头颈部鳞状细胞癌 (HNSCC) 的病因学和发病机制中发挥重要作用。本研究从 GEO 数据库中下载了甲基化微阵列数据集 (GSE87053) 和基因表达微阵列数据集 (GSE23558),并通过 R 语言进行分析。最终确定了 255 个高甲基化下调基因和 114 个低甲基化上调基因。进行了功能富集分析,并构建了一个综合的蛋白质-蛋白质相互作用 (PPI) 网络。随后,通过 Cytoscape 软件选择了前 10 个枢纽基因进行进一步分析。结果表明,CSF2、CTLA4、ETS1、PIK3CD 和 CFTR 的表达水平与 HNSCC 密切相关。生存分析表明,CTLA4 和 FGFR2 可作为 HNSCC 患者有效的独立预后生物标志物。总的来说,我们的研究为进一步研究 HNSCC 癌变的潜在分子机制奠定了基础,为 HNSCC 提供了潜在的生物标志物和治疗靶点。