Department of Neurosurgery, Renmin Hospital of Wuhan University, 9 Zhangzhidong Road and 238 Jiefang Road, Wuchang, Wuhan, Hubei, 430060, People's Republic of China.
BMC Med Genomics. 2018 Nov 1;11(1):96. doi: 10.1186/s12920-018-0407-1.
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.
多形性胶质母细胞瘤是最常见和侵袭性的脑肿瘤,预后较差。胶质母细胞瘤发生的分子机制仍知之甚少。因此,包括各种标志物在内的分子研究对于了解胶质瘤的发生和发展是必要的。
对 TCGA 胶质母细胞瘤样本进行加权基因共表达网络分析(WGCNA),构建基因共表达网络。基因本体(GO)和通路富集分析用于鉴定基因模块的意义。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),并确定了一个与 TCGA 胶质母细胞瘤样本生存时间相关的基因模块(黄色模块)。然后,根据基因显著性(GS)和模块显著性(MS)计算了 228 个枢纽基因。选择四个基因(OSMR+SOX21+MED10+PTPRN)构建 Cox 比例风险回归模型,具有较高的准确性(AUC=0.905)。Cox 比例风险回归模型的预后价值也在 GSE16011 数据集(GBM:n=156)中得到了验证。
我们开发了一种有前途的 mRNA 标志物,可用于估计胶质母细胞瘤患者的总生存率。