Zhao Liang, Zhang Jiayue, Liu Zhiyuan, Zhao Peng
Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University Nanjing, Jiangsu, China.
Am J Transl Res. 2020 Apr 15;12(4):1222-1238. eCollection 2020.
Secondary glioblastoma (sGBM) is a type of glioblastoma multiforme that evolves from low-grade glioma (LGG). However, the mechanism of this transition still remains poorly understood. In this study, we used weighted gene co-expression network analysis (WGCNA) on the gene expression profiles of glioma samples from the Chinese Glioma Genome Atlas (CGGA) database to identify key genetic module related to distinguish histological characteristics. Here, the brown module was highly correlated with histological characteristics and was selected as the hub module. By applying functional annotation analysis, we found that biological processes related to the cell-cycle and DNA-replication were enriched in the genes of the brown module. After constructing a protein-protein interaction (PPI) network, validation of differential gene expression, and survival analyses, we ultimately identified five hub genes: CCNB2 (Cyclin B2), KIF2C (Kinesin Family Member 2C), CDC20 (Cell Division Cycle 20), TPX2 (TPX2 Microtubule Nucleation Factor), and PLK1 (Polo Like Kinase 1). In addition, a computational risk model was developed for predicting the clinical outcomes of sGBM patients by combining gene expression levels. This gene signature was demonstrated to be an independent predictor of survival by univariate and multivariable Cox regression analysis. Finally, we used the Genomics of Drug Sensitivity in Cancer (GDSC) database to predict the responses of sGBM patients to routine chemotherapeutic drugs. Patients from the high-risk group were more sensitive to common chemotherapies during clinical treatment. Our findings based on comprehensive analyses might advance the understanding of sGBM transition and aid the development of novel biomarkers for diagnosing and predicting the survival of sGBM patients.
继发性胶质母细胞瘤(sGBM)是一种多形性胶质母细胞瘤,由低级别胶质瘤(LGG)演变而来。然而,这种转变的机制仍知之甚少。在本研究中,我们对来自中国胶质瘤基因组图谱(CGGA)数据库的胶质瘤样本基因表达谱进行加权基因共表达网络分析(WGCNA),以识别与区分组织学特征相关的关键基因模块。在此,棕色模块与组织学特征高度相关,并被选为核心模块。通过功能注释分析,我们发现棕色模块的基因中富集了与细胞周期和DNA复制相关的生物学过程。构建蛋白质-蛋白质相互作用(PPI)网络、验证差异基因表达并进行生存分析后,我们最终确定了五个核心基因:CCNB2(细胞周期蛋白B2)、KIF2C(驱动蛋白家族成员2C)、CDC20(细胞分裂周期20)、TPX2(TPX2微管成核因子)和PLK1(波罗样激酶1)。此外,通过结合基因表达水平,开发了一种计算风险模型来预测sGBM患者的临床结局。单变量和多变量Cox回归分析表明,这种基因特征是生存的独立预测因子。最后,我们使用癌症药物敏感性基因组学(GDSC)数据库来预测sGBM患者对常规化疗药物的反应。高危组患者在临床治疗中对常用化疗更敏感。我们基于综合分析的研究结果可能会增进对sGBM转变的理解,并有助于开发用于诊断和预测sGBM患者生存的新型生物标志物。