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A cuproptosis-based prognostic model for predicting survival in low-grade glioma
Zongren Zhao1, Yuanhao Ma2,3, Yu Liu1,3
1Department of Neurosurgery, Affiliated Huaian Hospital of Xuzhou Medical University, Huaian 223002, China.
Aging
|May 13, 2024
Summary
Researchers developed a predictive model for low-grade gliomas (LGG) using cuproptosis-related genes. This model effectively stratifies patient prognosis and may improve therapeutic strategies for glioma.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Low-grade gliomas (LGG) lack defined contributing variables for their formation and multiplication.
- Cuproptosis is an emerging cell death process with an unknown role in LGG.
- Understanding cuproptosis-related genes is crucial for advancing LGG therapeutic options.
Purpose of the Study:
- To investigate the role of cuproptosis-related genes in LGG.
- To develop a prognostic risk model for LGG based on cuproptosis-associated genes.
- To enhance therapeutic strategies for LGG patients.
Main Methods:
- Utilized TCGA and CGGA databases for risk model development and external validation.
- Employed Cox analysis (univariate, multivariate, LASSO) and ROC curves for predictive ability assessment.
- Performed immunohistochemistry, gene mutation analysis, functional enrichment, and Western blot to validate findings.
Main Results:
- A five-gene cuproptosis signature was developed, demonstrating significant differences in overall survival (OS) between high- and low-risk groups.
- The risk model showed high predictive performance and correlated with clinical characteristics and molecular subgroups.
- Immunological analysis indicated distinct immune microenvironments between risk groups, with implications for immunotherapy and chemotherapy.
Conclusions:
- A novel prediction model for LGG patients based on cuproptosis-associated genes was successfully developed.
- The risk model exhibits acceptable predictive performance for stratifying glioma patient prognosis.
- This study provides a foundation for targeted therapies and improved management of LGG.

