Uncovering novel functions of NUF2 in glioblastoma and MRI-based expression prediction
Glioblastoma multiforme (GBM) is a lethal brain tumor with limited therapies. NUF2, a kinetochore protein involved in cell cycle regulation, shows oncogenic potential in various cancers; however, its role in GBM pathogenesis remains unclear. In this study, we investigated NUF2's function and mechanisms in GBM and developed an MRI-based machine learning model to predict its expression non-invasively, and evaluated its potential as a therapeutic target and prognostic biomarker. Functional assays (proliferation, colony formation, migration, and invasion) and cell cycle analysis were conducted using NUF2-knockdown U87/U251 cells. Western blotting was performed to assess the expression levels of β-catenin and MMP-9. Bioinformatic analyses included pathway enrichment, immune infiltration, and single-cell subtype characterization. Using preoperative T1CE Magnetic Resonance Imaging sequences from 61 patients, we extracted 1037 radiomic features and developed a predictive model using Least Absolute Shrinkage and Selection Operator regression for feature selection and random forest algorithms for classification with rigorous cross-validation. NUF2 overexpression in GBM tissues and cells was correlated with poor survival (p < 0.01). Knockdown of NUF2 significantly suppressed malignant phenotypes (p < 0.05), induced G0/G1 arrest (p < 0.01), and increased sensitivity to TMZ treatment via the β-catenin/MMP9 pathway. The radiomic model achieved superior NUF2 prediction (AUC = 0.897) using six optimized features. Key features demonstrated associations with MGMT methylation and 1p/19q co-deletion, serving as independent prognostic markers. NUF2 drives GBM progression through β-catenin/MMP9 activation, establishing its dual role as a therapeutic target and a prognostic biomarker. The developed radiogenomic model enables precise non-invasive NUF2 evaluation, thereby advancing personalized GBM management. This study highlights the translational value of integrating molecular biology with artificial intelligence in neuro-oncology.
Authors
- Zengwei Kou (ORCID: https://orcid.org/0009-0004-8779-7186)
- Ray Y. Zhong (ORCID: https://orcid.org/0000-0002-3011-2009)
- Han Tang (ORCID: https://orcid.org/0000-0002-2732-9573)
- Guodong Huang (ORCID: https://orcid.org/0000-0002-2848-7581)
- Qian Li (ORCID: https://orcid.org/0000-0003-4657-1020)
- Yuan Zhang (ORCID: https://orcid.org/0000-0002-3225-2769)
- Na Zhang (ORCID: https://orcid.org/0000-0002-5510-5702)
- Fanfan Chen (ORCID: https://orcid.org/0000-0003-0425-7420)
- Heng Wang (ORCID: https://orcid.org/0000-0003-1485-7032)
- Yunsheng Liu
Institutions
- Guangzhou University of Chinese Medicine (CN)
- Shenzhen University (CN)
- University of Toronto (CA)
- First Affiliated Hospital of University of South China (CN)
- Shenzhen Institutes of Advanced Technology (CN)
- Shenzhen Second People's Hospital (CN)
- University of South China (CN)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-09-01
- DOI
- https://doi.org/10.1038/s41598-025-15721-2
- Citations
- 1
- Primary Topic
- RNA modifications and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- Sanming Project of Medicine in Shenzhen