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头颈部鳞状细胞癌中的差异基因表达和网络分析。

Differential gene expression and network analysis in head and neck squamous cell carcinoma.

机构信息

Department of Computer Science, Jamia Millia Islamia, Jamia Nagar, New Delhi, 110025, India.

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif, 21944, Saudi Arabia.

出版信息

Mol Cell Biochem. 2022 May;477(5):1361-1370. doi: 10.1007/s11010-022-04379-3. Epub 2022 Feb 10.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a prevalent malignancy with a poor prognosis, whose biomarkers have not been studied in great detail. We have collected genomic data of HNSCC patients from The Cancer Genome Atlas (TCGA) and analyzed them to get deeper insights into the gene expression pattern. Initially, 793 differentially expressed genes (DEGs) were categorized, and their enrichment analysis was performed. Later, a protein-protein interaction network for the DEGs was constructed using the STRING plugin in Cytoscape to study their interactions. A set of 10 hub genes was selected based on Maximal Clique Centrality score, and later their survival analysis was studied. The elucidated set of 10 genes, i.e., PRAME, MAGEC2, MAGEA12, LHX1, MAGEA3, CSAG1, MAGEA6, LCE6A, LCE2D, LCE2C, referred to as potential candidates to be explored as HNSCC biomarkers. The Kaplan-Meier overall survival of the selected genes suggested that the alterations in the candidate genes were linked to the decreased survival of the HNSCC patients. Altogether, the results of this study signify that the genomic alterations and differential expression of the selected genes can be explored in therapeutic interpolations of HNSCC, exploiting early diagnosis and target-propelled therapy.

摘要

头颈部鳞状细胞癌(HNSCC)是一种普遍存在且预后不良的恶性肿瘤,其生物标志物尚未得到详细研究。我们从癌症基因组图谱(TCGA)收集了 HNSCC 患者的基因组数据,并对其进行了分析,以更深入地了解基因表达模式。最初,我们对 793 个差异表达基因(DEGs)进行了分类,并对其进行了富集分析。随后,我们使用 Cytoscape 中的 STRING 插件构建了 DEGs 的蛋白质-蛋白质相互作用网络,以研究它们的相互作用。根据最大团中心度评分,选择了一组 10 个枢纽基因,并进一步研究了它们的生存分析。阐明的 10 个基因集,即 PRAME、MAGEC2、MAGEA12、LHX1、MAGEA3、CSAG1、MAGEA6、LCE6A、LCE2D、LCE2C,被认为是探索 HNSCC 生物标志物的潜在候选基因。选定基因的 Kaplan-Meier 总体生存分析表明,候选基因的改变与 HNSCC 患者生存时间的缩短有关。总之,这项研究的结果表明,所选基因的基因组改变和差异表达可以在 HNSCC 的治疗干预中进行探索,利用早期诊断和靶向治疗。

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