Integrated profiling identifies ferredoxin 1 as an immune-related biomarker of malignant phenotype in glioma
View abstract on PubMed
Summary
This summary is machine-generated.Ferredoxin 1 (FDX1) is upregulated in glioma, correlating with poor prognosis and increased immune cell infiltration. Targeting FDX1 may offer new therapeutic strategies for this challenging brain tumor.
Area Of Science
- Neuro-oncology
- Cancer immunology
- Cell death mechanisms
Background
- Glioma is a challenging central nervous system tumor known for resistance to treatment and high recurrence rates.
- Ferredoxin 1 (FDX1) plays a role in cuproptosis (a cell death pathway), but its prognostic significance in glioma and impact on tumor immunity are unclear.
Purpose Of The Study
- To investigate the prognostic value of FDX1 in glioma.
- To explore the relationship between FDX1 expression and tumor immune infiltration.
- To elucidate the biological function of FDX1 in glioma cells.
Main Methods
- Pan-cancer data analysis using public databases.
- Gene expression analysis via tissue microarray and single-cell sequencing.
- Prognostic assessment, differential gene expression, and Gene Set Enrichment Analysis (GSEA).
- Tumor Mutation Burden (TMB) and immune cell infiltration analysis.
- In vitro experiments on FDX1 knockdown in glioma cells.
Main Results
- FDX1 was upregulated in glioma and associated with poor prognosis and adverse clinicopathological features.
- Immune-related signaling pathways were enriched, linking FDX1 expression to mutation frequency and TMB.
- Higher FDX1 expression correlated with increased immune cell infiltration and immune checkpoint regulation.
- In vitro knockdown of FDX1 inhibited glioma cell proliferation, migration, invasion, and cell cycle progression.
Conclusions
- FDX1 expression is positively associated with glioma malignancy and altered immune cell infiltration.
- FDX1 may serve as a prognostic biomarker and a potential therapeutic target in glioma.

