Identification of a Novel Eight-Gene Risk Model for Predicting Survival in Glioblastoma: A Comprehensive Bioinformatic Analysis

Author:

Dang Huy-Hoang1,Ta Hoang Dang Khoa23ORCID,Nguyen Truc Tran Thanh4ORCID,Wang Chih-Yang23ORCID,Lee Kuen-Haur235ORCID,Le Nguyen Quoc Khanh6789ORCID

Affiliation:

1. International Ph.D. Program for Cell Therapy and Regeneration Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan

2. Ph.D. Program for Cancer Molecular Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University and Academia Sinica, Taipei 110, Taiwan

3. Graduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 110, Taiwan

4. Taiwan International Graduate Program in Interdisciplinary Neuroscience, National Taiwan University and Academia Sinica, Taipei 115, Taiwan

5. Cancer Center, Wan Fang Hospital, Taipei Medical University, Taipei 110, Taiwan

6. Professional Master Program in Artificial Intelligence in Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan

7. AIBioMed Research Group, Taipei Medical University, Taipei 110, Taiwan

8. Research Center for Artificial Intelligence in Medicine, Taipei Medical University, Taipei 110, Taiwan

9. Translational Imaging Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan

Abstract

Glioblastoma (GBM) is one of the most progressive and prevalent cancers of the central nervous system. Identifying genetic markers is therefore crucial to predict prognosis and enhance treatment effectiveness in GBM. To this end, we obtained gene expression data of GBM from TCGA and GEO datasets and identified differentially expressed genes (DEGs), which were overlapped and used for survival analysis with univariate Cox regression. Next, the genes’ biological significance and potential as immunotherapy candidates were examined using functional enrichment and immune infiltration analysis. Eight prognostic-related DEGs in GBM were identified, namely CRNDE, NRXN3, POPDC3, PTPRN, PTPRN2, SLC46A2, TIMP1, and TNFSF9. The derived risk model showed robustness in identifying patient subgroups with significantly poorer overall survival, as well as those with distinct GBM molecular subtypes and MGMT status. Furthermore, several correlations between the expression of the prognostic genes and immune infiltration cells were discovered. Overall, we propose a survival-derived risk score that can provide prognostic significance and guide therapeutic strategies for patients with GBM.

Funder

Taiwan Higher Education Sprout Project by the Ministry of Education

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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