Bu Fan, Zhong Jifa, Guan Ruiqian
The Third Affiliated Hospital of Xinxiang Medical University, Xinxiang, Henan, China.
Heilongjiang University of Chinese Medicine Affiliated Second Hospital, Harbin, China.
Front Mol Biosci. 2025 Mar 18;12:1506961. doi: 10.3389/fmolb.2025.1506961. eCollection 2025.
Discovering biomarkers is central to the research and treatment of degenerative central nervous system (CNS) diseases, playing a crucial role in early diagnosis, disease monitoring, and the development of new treatments, particularly for challenging conditions like degenerative CNS diseases and glioblastoma (GBM).
This study analyzed gene expression data from a public database, employing differential expression analyses and Gene Co-expression Network Analysis (WGCNA) to identify gene modules associated with degenerative CNS diseases and GBM. Machine learning methods, including Random Forest, Least Absolute Shrinkage and Selection Operator (LASSO), and Support Vector Machine - Recursive Feature Elimination (SVM-RFE), were used for case-control differentiation, complemented by functional enrichment analysis and external validation of key genes.
Ninety-five commonly altered genes related to degenerative CNS diseases and GBM were identified, with and emerging as significant through machine learning screening. Receiver operating characteristic (ROC) analysis confirmed their diagnostic value, which was further validated externally, indicating their elevated expression in controls.
The study's integration of WGCNA and machine learning uncovered and as potential biomarkers for degenerative CNS diseases and GBM, suggesting their utility in diagnostics and as therapeutic targets. This contributes new perspectives on the pathogenesis and treatment of these complex conditions.
发现生物标志物是退行性中枢神经系统(CNS)疾病研究和治疗的核心,在早期诊断、疾病监测以及新治疗方法的开发中发挥着关键作用,尤其是对于退行性CNS疾病和胶质母细胞瘤(GBM)等具有挑战性的病症。
本研究分析了来自公共数据库的基因表达数据,采用差异表达分析和基因共表达网络分析(WGCNA)来识别与退行性CNS疾病和GBM相关的基因模块。机器学习方法,包括随机森林、最小绝对收缩和选择算子(LASSO)以及支持向量机-递归特征消除(SVM-RFE),用于病例对照区分,并辅以功能富集分析和关键基因的外部验证。
鉴定出95个与退行性CNS疾病和GBM相关的常见改变基因,通过机器学习筛选,[具体基因1]和[具体基因2]显示出显著性。受试者工作特征(ROC)分析证实了它们的诊断价值,并在外部进一步验证,表明它们在对照组中表达升高。
该研究将WGCNA和机器学习相结合,发现[具体基因1]和[具体基因2]是退行性CNS疾病和GBM的潜在生物标志物,表明它们在诊断和作为治疗靶点方面的效用。这为这些复杂病症的发病机制和治疗提供了新的视角。