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Identification of glioblastoma?gene prognosis modules based on weighted gene co-expression network analysis

机译:基于加权基因共表达网络分析的胶质母细胞瘤基因预后模块的鉴定

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Glioblastoma multiforme, the most prevalent and aggressive brain tumour, has a poor prognosis. The molecular mechanisms underlying gliomagenesis remain poorly understood. Therefore, molecular research, including various markers, is necessary to understand the occurrence and development of glioma. Weighted gene co-expression network analysis (WGCNA) was performed to construct a gene co-expression network in TCGA glioblastoma samples. Gene ontology (GO) and pathway-enrichment analysis were used to identify significance of gene modules. Cox proportional hazards regression model was used to predict outcome of glioblastoma patients. We performed weighted gene co-expression network analysis (WGCNA) and identified a gene module (yellow module) related to the survival time of TCGA glioblastoma samples. Then, 228 hub genes were calculated based on gene significance (GS) and module significance (MS). Four genes (OSMR + SOX21?+?MED10?+?PTPRN) were selected to construct a Cox proportional hazards regression model with high accuracy (AUC?=?0.905). The prognostic value of the Cox proportional hazards regression model was also confirmed in GSE16011 dataset (GBM: n?=?156). We developed a promising mRNA signature for estimating overall survival in glioblastoma patients.
机译:多形性胶质母细胞瘤是最普遍,最具侵略性的脑肿瘤,预后较差。胶质瘤发生的分子机制仍知之甚少。因此,包括各种标记物在内的分子研究对于了解神经胶质瘤的发生和发展是必要的。进行加权基因共表达网络分析(WGCNA),以在TCGA胶质母细胞瘤样品中构建基因共表达网络。基因本体论(GO)和途径富集分析被用来确定基因模块的重要性。 Cox比例风险回归模型用于预测胶质母细胞瘤患者的预后。我们进行了加权基因共表达网络分析(WGCNA),并确定了与TCGA胶质母细胞瘤样品的生存时间有关的基因模块(黄色模块)。然后,基于基因重要性(GS)和模块重要性(MS)计算了228个集线器基因。选择四个基因(OSMR + SOX21 + + MED10 + + PTPRN)来构建高精度的Cox比例风险回归模型(AUC = = 0.905)。 Cox比例风险回归模型的预后价值也在GSE16011数据集中得到了证实(GBM:n == 156)。我们开发了有前途的mRNA签名,用于估计胶质母细胞瘤患者的总体生存率。

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