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Distinct co-expression networks using multi-omic data reveal novel interventional targets in HPV-positive and negative head-and-neck squamous cell cancer

机译:使用多组学数据的不同共表达网络揭示了HPV阳性和阴性头颈鳞状细胞癌的新型介入靶标

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摘要

The human papillomavirus (HPV) is present in a significant fraction of head-and-neck squamous cell cancer (HNSCC). The main goal of this study was to identify distinct co-expression patterns between HPV+ and HPV− HNSCC and to provide insights into potential regulatory mechanisms/effects within the analyzed networks. We selected cases deposited in The Cancer Genome Atlas database comprising data of gene expression, methylation profiles and mutational patterns, in addition to clinical information. The intersection among differentially expressed and differentially methylated genes showed the negative correlations between the levels of methylation and expression, suggesting that these genes have their expression levels regulated by methylation alteration patterns in their promoter. Weighted correlation network analysis was used to identify co-expression modules and a systematic approach was applied to refine them and identify key regulatory elements integrating results from the other omics. Three distinct co-expression modules were associated with HPV status and molecular signatures. Validation using independent studies reporting biological experimental data converged for the most significant genes in all modules. This study provides insights into complex genetic and epigenetic particularities in the development and progression of HNSCC according to HPV status, and contribute to unveiling specific genes/pathways as novel therapeutic targets in HNSCC.
机译:人乳头瘤病毒(HPV)存在于很大一部分的头颈鳞状细胞癌(HNSCC)中。这项研究的主要目标是确定HPV +和HPV- HNSCC之间的独特共表达模式,并提供对所分析网络中潜在调控机制/效应的见解。我们选择了存放在《癌症基因组图谱》数据库中的病例,其中除了临床信息外,还包括基因表达,甲基化谱和突变模式的数据。差异表达和差异甲基化基因之间的相交显示了甲基化水平与表达之间的负相关,表明这些基因的表达水平受其启动子中甲基化改变模式的调节。加权相关网络分析用于识别共表达模块,并应用系统方法对其进行优化,并确定整合其他组学结果的关键调控元件。三个不同的共表达模块与HPV状态和分子标记相关。使用报告生物学实验数据的独立研究进行的验证,验证了所有模块中最重要的基因的融合。这项研究根据HPV的状态,为HNSCC的发展和进程中复杂的遗传和表观遗传学特性提供了见识,并有助于揭示作为HNSCC新型治疗靶点的特定基因/途径。

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