Published October 21, 2026 | Version v1

Ferroptosis and Cuproptosis in the Pathogenesis of Breast Cancer: Molecular Mechanisms, Crosstalk, and Therapeutic Perspectives

  • 1. Independent Researcher

Description

The essay reviews current understanding of the role of metal-dependent forms of regulated cell death – ferroptosis and cuproptosis – in the pathogenesis of breast cancer and their therapeutic potential. The aim of the work was to analyze the molecular mechanisms of both processes, identify common regulatory nodes, and assess the prospects for their joint targeting to overcome chemoresistance. Methodologically, the work is based on a critical review of peer-reviewed scientific sources devoted to ferroptosis, cuproptosis, and their cross-talk in the context of oncology. It has been shown that ferroptosis, iron-dependent lipid peroxidation, and cuproptosis, copper-dependent proteotoxic death, have common regulatory nodes, in particular, glutathione metabolism, mitochondrial respiration, and the p53 signaling pathway. It has been established that induction of both processes allows overcoming resistance to cisplatin, doxorubicin, and taxanes, especially in aggressive subtypes such as triple-negative breast cancer. Current therapeutic strategies are reviewed, including the use of nanocarriers for targeted delivery of ferroptosis and cuproptosis inducers, as well as the results of clinical trials of disulfiram, elesclomol, and copper chelators. At the same time, limitations of clinical translation are emphasized: the lack of validated biomarkers, the risk of systemic toxicity, and tumor heterogeneity. It is concluded that co-targeting ferroptosis and cuproptosis is a promising strategy, but its widespread clinical application requires further prospective studies, biomarker identification, and development of targeted nanosystems.

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2026-10-21

References

  • 1. Bray, F.; Laversanne, M.; Sung, H.; Ferlay, J.; Siegel, R.L.; Soerjomataram, I.; Jemal, A. Global Cancer Statistics 2022: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA. Cancer J. Clin. 2024, 74, 229–263. https://doi.org/10.3322/caac.21834 2. Ivchuk, V. Chronic Inflammation as an Underlying Pathogenetic Mechanism of Chronic Non-Communicable Diseases: Molecular, Cellular, and Therapeutic Dimensions. Preprints 2026, 2026092666. https://doi.org/10.20944/preprints202609.2666.v1 3. Imam, M.; Ji, J.; Zhang, Z.; Yan, S. Targeting the Initiator to Activate Both Ferroptosis and Cuproptosis for Breast Cancer Treatment: Progress and Possibility for Clinical Application. Front. Pharmacol. 2025, 15, 1493188. https://doi.org/10.3389/fphar.2024.1493188 4. Dixon, S.J.; Lemberg, K.M.; Lamprecht, M.R.; Skouta, R.; Zaitsev, E.M.; Gleason, C.E.; Patel, D.N.; Bauer, A.J.; Cantley, A.M.; Yang, W.S.; et al. Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death. Cell 2012, 149, 1060–1072. https://doi.org/10.1016/j.cell.2012.03.042 5. Ivchuk, V. Ferroptosis: Molecular Mechanisms of Regulation and Therapeutic Potential in the Pathogenesis of Multifactorial Diseases. Preprints 2026, 2026090771. https://doi.org/10.20944/preprints202609.0771.v1 6. Koppula, P.; Zhuang, L.; Gan, B. Cystine Transporter SLC7A11/xCT in Cancer: Ferroptosis, Nutrient Dependency, and Cancer Therapy. Protein Cell 2021, 12, 599–620. https://doi.org/10.1007/s13238-020-00789-5 7. Doll, S.; Proneth, B.; Tyurina, Y.Y.; Panzilius, E.; Kobayashi, S.; Ingold, I.; Irmler, M.; Beckers, J.; Aichler, M.; Walch, A.; et al. ACSL4 Dictates Ferroptosis Sensitivity by Shaping Cellular Lipid Composition. Nat. Chem. Biol. 2017, 13, 91–98. https://doi.org/10.1038/nchembio.2239 8. Fang, X.; Ardehali, H.; Min, J.; Wang, F. The Molecular and Metabolic Landscape of Iron and Ferroptosis in Cardiovascular Disease. Nat. Rev. Cardiol. 2023, 20, 7–23. https://doi.org/10.1038/s41569-022-00735-4 9. Bersuker, K.; Hendricks, J.M.; Li, Z.; Magtanong, L.; Ford, B.; Tang, P.H.; Roberts, M.A.; Tong, B.; Maimone, T.J.; Zoncu, R.; et al. The CoQ Oxidoreductase FSP1 Acts Parallel to GPX4 to Inhibit Ferroptosis. Nature 2019, 575, 688–692. https://doi.org/10.1038/s41586-019-1705-2 10. Chen, X.; Kang, R.; Kroemer, G.; Tang, D. Broadening Horizons: The Role of Ferroptosis in Cancer. Nat. Rev. Clin. Oncol. 2021, 18, 280–296. https://doi.org/10.1038/s41571-020-00462-0 11. Wang, L.; Wang, C.; Li, X.; Tao, Z.; Zhu, W.; Su, Y.; Choi, W.S. Melatonin and Erastin Emerge Synergistic Anti-Tumor Effects on Oral Squamous Cell Carcinoma by Inducing Apoptosis, Ferroptosis, and Inhibiting Autophagy through Promoting ROS. Cell. Mol. Biol. Lett. 2023, 28, 36. https://doi.org/10.1186/s11658-023-00449-6 12. Tsvetkov, P.; Coy, S.; Petrova, B.; Dreishpoon, M.; Verma, A.; Abdusamad, M.; Rossen, J.; Joesch-Cohen, L.; Humeidi, R.; Spangler, R.D.; et al. Copper Induces Cell Death by Targeting Lipoylated TCA Cycle Proteins. Science 2022, 375, 1254–1261. https://doi.org/10.1126/science.abf0529 13. Dreishpoon, M.B.; Bick, N.R.; Petrova, B.; Warui, D.M.; Cameron, A.; Booker, S.J.; Kanarek, N.; Golub, T.R.; Tsvetkov, P. FDX1 Regulates Cellular Protein Lipoylation through Direct Binding to LIAS. J. Biol. Chem. 2023, 299, 105046. https://doi.org/10.1016/j.jbc.2023.105046 14. Tang, Y.; Lv, C.; Luo, Z.; Li, Z.; Yu, J. Construction of a Prognostic Model Based on Cuproptosis-Related Patterns for Predicting Survival, Immune Infiltration, and Immunotherapy Efficacy in Breast Cancer: Cuproptosis-Based Prognostic Modeling in Breast Cancer. Medicine (Baltimore) 2024, 103, e40136. https://doi.org/10.1097/MD.0000000000040136 15. Ivchuk, V. Cuproptosis: Biochemical Mechanisms, Therapeutic Potential, and Clinical Challenges. Preprints 2026, 2026101523. https://doi.org/10.20944/preprints202610.1523.v1 16. Zheng, P.; Zhou, C.; Lu, L.; Liu, B.; Ding, Y. Elesclomol: A Copper Ionophore Targeting Mitochondrial Metabolism for Cancer Therapy. J. Exp. Clin. Cancer Res. 2022, 41, 271. https://doi.org/10.1186/s13046-022-02485-0 17. Guo, X.; Xu, B.; Pandey, S.; Goessl, E.; Brown, J.; Armesilla, A.L.; Darling, J.L.; Wang, W. Disulfiram/Copper Complex Inhibiting NFκB Activity and Potentiating Cytotoxic Effect of Gemcitabine on Colon and Breast Cancer Cell Lines. Cancer Lett. 2010, 290, 104–113. https://doi.org/10.1016/j.canlet.2009.09.002 18. Zhang, P.; Zhou, C.; Ren, X.; Jing, Q.; Gao, Y.; Yang, C.; Shen, Y.; Zhou, Y.; Hu, W.; Jin, F.; et al. Inhibiting the Compensatory Elevation of xCT Collaborates with Disulfiram/Copper-Induced GSH Consumption for Cascade Ferroptosis and Cuproptosis. Redox Biol. 2024, 69, 103007. https://doi.org/10.1016/j.redox.2023.103007 19. Tang, D.; Chen, X.; Kroemer, G. Cuproptosis: A Copper-Triggered Modality of Mitochondrial Cell Death. Cell Res. 2022, 32, 417–418. https://doi.org/10.1038/s41422-022-00653-7 20. Xiong, C.; Ling, H.; Hao, Q.; Zhou, X. Cuproptosis: P53-Regulated Metabolic Cell Death? Cell Death Differ. 2023, 30, 876–884. https://doi.org/10.1038/s41418-023-01125-0 21. Xue, Q.; Yan, D.; Chen, X.; Li, X.; Kang, R.; Klionsky, D.J.; Kroemer, G.; Chen, X.; Tang, D.; Liu, J. Copper-Dependent Autophagic Degradation of GPX4 Drives Ferroptosis. Autophagy 2023, 19, 1982–1996. https://doi.org/10.1080/15548627.2023.2165323 22. Wang, W.; Lu, K.; Jiang, X.; Wei, Q.; Zhu, L.; Wang, X.; Jin, H.; Feng, L. Ferroptosis Inducers Enhanced Cuproptosis Induced by Copper Ionophores in Primary Liver Cancer. J. Exp. Clin. Cancer Res. 2023, 42, 142. https://doi.org/10.1186/s13046-023-02720-2 23. Gao, W.; Huang, Z.; Duan, J.; Nice, E.C.; Lin, J.; Huang, C. Elesclomol Induces Copper‐dependent Ferroptosis in Colorectal Cancer Cells via Degradation of ATP7A. Mol. Oncol. 2021, 15, 3527–3544. https://doi.org/10.1002/1878-0261.13079 24. Li, Y.; Du, Y.; Zhou, Y.; Chen, Q.; Luo, Z.; Ren, Y.; Chen, X.; Chen, G. Iron and Copper: Critical Executioners of Ferroptosis, Cuproptosis and Other Forms of Cell Death. Cell Commun. Signal. 2023, 21, 327. https://doi.org/10.1186/s12964-023-01267-1 25. Li, Y.; Liu, J.; Chen, Y.; Weichselbaum, R.R.; Lin, W. Nanoparticles Synergize Ferroptosis and Cuproptosis to Potentiate Cancer Immunotherapy. Adv. Sci. 2024, 11, 2310309. https://doi.org/10.1002/advs.202310309 26. Chen, K.; Zhou, A.; Zhou, X.; He, J.; Xu, Y.; Ning, X. Cellular Trojan Horse Initiates Bimetallic Fe-Cu MOF-Mediated Synergistic Cuproptosis and Ferroptosis against Malignancies. Sci. Adv. 2024, 10, eadk3201. https://doi.org/10.1126/sciadv.adk3201 27. O'Day, S.J.; Eggermont, A.M.M.; Chiarion-Sileni, V.; Kefford, R.; Grob, J.J.; Mortier, L.; Robert, C.; Schachter, J.; Testori, A.; Mackiewicz, J.; et al. Final Results of Phase III SYMMETRY Study: Randomized, Double-Blind Trial of Elesclomol Plus Paclitaxel Versus Paclitaxel Alone As Treatment for Chemotherapy-Naive Patients With Advanced Melanoma. J. Clin. Oncol. 2013, 31, 1211–1218. https://doi.org/10.1200/JCO.2012.44.5585 28. Hu, K.; Qiu, J.; Hu, Y.; Wang, Y.; Yu, C.; Wu, Y. Efficacy of FERscore in Predicting Sensitivity to Ferroptosis Inducers in Breast Cancer. NPJ Breast Cancer 2024, 10, 74. https://doi.org/10.1038/s41523-024-00685-9 29. Koppula, P.; Lei, G.; Zhang, Y.; Yan, Y.; Mao, C.; Kondiparthi, L.; Shi, J.; Liu, X.; Horbath, A.; Das, M.; et al. A Targetable CoQ-FSP1 Axis Drives Ferroptosis- and Radiation-Resistance in KEAP1 Inactive Lung Cancers. Nat. Commun. 2022, 13, 2206. https://doi.org/10.1038/s41467-022-29905-1 30. Yang, F.; Xiao, Y.; Ding, J.-H.; Jin, X.; Ma, D.; Li, D.-Q.; Shi, J.-X.; Huang, W.; Wang, Y.-P.; Jiang, Y.-Z.; et al. Ferroptosis Heterogeneity in Triple-Negative Breast Cancer Reveals an Innovative Immunotherapy Combination Strategy. Cell Metab. 2023, 35, 84-100.e8. https://doi.org/10.1016/j.cmet.2022.09.021