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Updated: Jun 26, 2026

Transposon Mediated Integration of Plasmid DNA into the Subventricular Zone of Neonatal Mice to Generate Novel Models of Glioblastoma
Published on: February 22, 2015
Integrative multi-platform gene expression and machine learning analysis for glioblastoma biomarker discovery with
Haseeb Nisar1,2, Ali Islam3, Amna Arshad2
1IRC for Finance and Digital Economy, King Fahd University of Petroleum and Minerals (KFUPM), Dhahran, Saudi Arabia.
Background:
Glioblastoma (GBM) is a highly aggressive form of brain tumor with poor prognosis. This study aimed to identify genes critical to glioma development and assess their potential diagnostic and therapeutic value through an integrated analysis of microarray and RNA-Seq datasets.
Methods:
We used data integration to improve statistical robustness and reliability. LASSO regression, along with seven machine learning classifiers, was utilized to find the most important features. The classifier performance was validated on unseen datasets, where SVM and kNN showed the highest accuracy. Functional enrichment analysis was performed on the selected features to assess their biological relevance, followed by validation of biomarkers through qPCR.
Results:
We identified three key genes, PLOD1, COL4A2, and COL5A2, that emerged as consistently top-ranked across models. Survival analysis revealed PLOD1 is the only gene significantly associated with poor prognosis in GBM. Further validation in patient samples confirmed a strong association between high PLOD1 expression and GBM, highlighting its potential as a diagnostic biomarker and therapeutic target.
Conclusion:
This robust integrative machine learning approach for biomarker discovery in GBM supports the development of more personalized treatment strategies.
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