# Role of Ferredoxin 1 (FDX1) in cancer and its therapeutic potential

**Authors:** Fen He, Hongyan Zhao, Ruixin Gao, Maoyou Lu, Siqi Wang, Yu Chen, Lijun Peng, Jiliang Xia

PMC · DOI: 10.1016/j.cpt.2025.11.002 · Cancer Pathogenesis and Therapy · 2025-11-07

## TL;DR

FDX1, a mitochondrial protein, is linked to cancer progression and immune responses, and may serve as a potential biomarker and therapeutic target.

## Contribution

This review highlights FDX1's dual roles in cancer and its potential as a mediator of cuproptosis and immunotherapy target.

## Key findings

- FDX1 expression is dysregulated in various cancers, with both upregulation and downregulation observed.
- FDX1 mediates cuproptosis, a copper-dependent cell death mechanism, suggesting tumor-suppressive roles.
- FDX1 correlates with tumor immunity and may act as a biomarker for cancer prognosis and immunotherapy response.

## Abstract

Ferredoxin 1 (FDX1) is a small iron-sulfur (Fe–S) cluster protein localized to the mitochondria. It functions as an electron carrier in diverse metabolic pathways and is critically involved in regulating protein lipoylation Accumulating evidence indicates that FDX1 expression is frequently dysregulated across various cancer types. Its expression is significantly associated with cancer progression, prognosis, and tumor immune responses, suggesting its potential as a biomarker for cancer diagnosis, prognostic evaluation, and immunotherapy response prediction. Transcription factors, epigenetic modifications, and non-coding RNAs (ncRNAs) contribute to the aberrant expression of FDX1 in cancer cells. Mechanistic studies reveal that FDX1 protein influences cancer progression by modulating oncogenic signaling pathways, metabolic reprogramming, and tumor immunity; Notably, FDX1 serves as a central mediator of cuproptosis — a copper-dependent form of programmed cell death — highlighting its potential tumor-suppressive function. Therefore, FDX1 may exert dual roles in cancer by either promoting or inhibiting disease progression. Recently, several agents targeting FDX1 have exhibited promising therapeutic efficacy both in vitro and in vivo across diverse cancer models. In this review, we summarize the regulatory mechanisms governing FDX1 expression and its functional roles in cancer progression. We also highlight its potential as a therapeutic target in cancer therapy.

Image 1

•Ferredoxin 1 (FDX1) expression is dysregulated in various cancer types, either upregulation or downregulation.•FDX1 plays a dual roles in different cancer types, exhibiting both tumor-promoting and tumor-suppressive functions•FDX1 is a key mediator of cuproptosis; therefore, elevating its expression or activity sensitizes cancer to cuproptosis.•FDX1 expression correlates with tumor immunity, suggesting it is a biomarker and therapeutic target for immunotherapy.

Ferredoxin 1 (FDX1) expression is dysregulated in various cancer types, either upregulation or downregulation.

FDX1 plays a dual roles in different cancer types, exhibiting both tumor-promoting and tumor-suppressive functions

FDX1 is a key mediator of cuproptosis; therefore, elevating its expression or activity sensitizes cancer to cuproptosis.

FDX1 expression correlates with tumor immunity, suggesting it is a biomarker and therapeutic target for immunotherapy.

## Linked entities

- **Genes:** FDX1 (ferredoxin 1) [NCBI Gene 2230]
- **Proteins:** FDX1 (ferredoxin 1)

## Full-text entities

- **Genes:** FDX1 (ferredoxin 1) [NCBI Gene 2230] {aka ADX, FDX, LOH11CR1D}
- **Diseases:** cancer (MESH:D009369)
- **Chemicals:** iron-sulfur (-), copper (MESH:D003300), Fe-S (MESH:D007501)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12992101/full.md

## References

132 references — full list in the complete paper: https://tomesphere.com/paper/PMC12992101/full.md

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Source: https://tomesphere.com/paper/PMC12992101