Systematic Reviews and Meta Analysis
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The Role of Iron Chelation Therapy in Prostate Cancer

Year 2025, Volume: 4 Issue: 2, 116 - 132, 13.12.2025
https://doi.org/10.5281/zenodo.17786796

Abstract

Prostate cancer remains a significant clinical challenge despite advances in current therapeutic modalities, with its progression to advanced stages closely associated with profound metabolic reprogramming, including disrupted iron homeostasis. Emerging evidence demonstrates that prostate cancer cells exhibit an “iron addiction,” characterized by enhanced expression of iron import proteins and suppression of iron export pathways, thereby fulfilling their elevated proliferative and metabolic requirements. Iron chelation therapy has consequently gained attention as a promising approach to target these iron-dependent processes by limiting intracellular iron availability, leading to the disruption of essential enzymes, signaling pathways, and redox balance. This review summarizes the mechanistic rationale, preclinical findings, and clinical hurdles related to the application of iron chelators in prostate cancer treatment. Furthermore, novel chelating agents and combination strategies are highlighted, with a focus on addressing limitations encountered in early clinical trials. Collectively, current evidence suggests that targeting iron metabolism holds considerable potential as a complementary strategy to enhance the efficacy of conventional therapies in prostate cancer management.

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There are 64 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other)
Journal Section Systematic Reviews and Meta Analysis
Authors

Mesut Akyüz 0000-0001-8161-2479

Elanur Aydın Karataş 0000-0001-8975-1932

Submission Date August 25, 2025
Acceptance Date October 11, 2025
Early Pub Date December 11, 2025
Publication Date December 13, 2025
Published in Issue Year 2025 Volume: 4 Issue: 2

Cite

APA Akyüz, M., & Aydın Karataş, E. (2025). The Role of Iron Chelation Therapy in Prostate Cancer. Eurasian Journal of Molecular and Biochemical Sciences, 4(2), 116-132. https://doi.org/10.5281/zenodo.17786796