AccScience Publishing / EJMO / Online First / DOI: 10.36922/EJMO026260298
Cite this article
4
Download
87
Views
Related Info Links
More by Authors Links
Journal Browser
Volume | Year
Issue
Search
News and Announcements
View All
REVIEW ARTICLE

Targeting pyroptosis, ferroptosis, and cuproptosis: An updated view of regulated cell death pathways for cancer therapy

Jing Zhao1 Xu Du1 Wei Fang1 Yingzhu Yan1 Zinan Li1 Hongxia Zhu1* Binglin Yue2*
Show Less
1 Department of Endocrinology, Chengdu Shuangliu Hospital of Traditional Chinese Medicine, Chengdu, Sichuan, China
2 Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Sichuan Province and Ministry of Education, Southwest Minzu University, Chengdu, Sichuan, China
Received: 22 June 2026 | Revised: 24 July 2026 | Accepted: 30 July 2026 | Published online: 6 August 2026
© 2026 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC-by the license) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Introduction: Cancer treatment has long relied on inducing apoptosis; however, tumors frequently develop resistance through apoptosis-evasion mechanisms, leading to recurrence and metastasis. In recent years, three emerging forms of programmed cell death—pyroptosis, ferroptosis, and cuproptosis—have attracted intense interest. Thanks to their distinct molecular pathways and strong immunogenic properties, they offer promising ways to overcome the limitations of traditional therapies. These mechanisms, driven by inflammatory signaling or dysregulation of metal ions (iron or copper), trigger mitochondrial dysfunction, lipid peroxidation, or membrane pore formation. Beyond directly killing tumor cells, they release damage-associated molecular patterns that activate immunogenic cell death. This process reshapes the tumor microenvironment and significantly enhances the efficacy of immune checkpoint inhibitors.

Objective: This review systematically summarizes the molecular regulation, network interactions, and therapeutic advances of these three novel cell death pathways, providing new theoretical foundations and potential translational strategies for treating refractory cancers.

Conclusion: Pyroptosis, ferroptosis, and cuproptosis represent interconnected, non-apoptotic cell death pathways with substantial potential to overcome therapeutic resistance, remodel the immunosuppressive tumor microenvironment, and enhance responses to immune checkpoint blockade. Further mechanistic validation, biomarker development, improved tumor-specific delivery, and well-designed clinical trials are required to translate these strategies into safe, precise, and effective cancer therapies.

Keywords
Cell death
Cancer therapy
Pyroptosis
Ferroptosis
Cuproptosis
Funding
The work was supported by the Sichuan Provincial Administration of Traditional Chinese Medicine under the Traditional Chinese Medicine Research Special Project (2024MS414) and by the Fundamental Research Funds for the Central Universities, Southwest Minzu University (ZYN2025026).
Conflict of interest
The authors declare no competing interests.
References
  1. Bray F, Laversanne M, Sung H, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229-263. doi: 10.3322/caac.21834
  2. Galluzzi L, Vitale I, Aaronson SA, et al. Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. Cell Death Differ. 2018;25(3):486-541. doi: 10.1038/s41418-017-0012-4
  3. Guo D, Guo Y, Zhu C, et al. Programmed cell death network in cancer drug resistance: a framework for therapeutic intervention. Drug Resist Updat. 2026;86:101387. doi: 10.1016/j.drup.2026.101387
  4. Zhang Y, Huang Q, Xu Q, Jia C, Xia Y. Pimavanserin tartrate induces apoptosis and cytoprotective autophagy and synergizes with chemotherapy on triple negative breast cancer. Biomed Pharmacother. 2023;168:115665. doi: 10.1016/j.biopha.2023.115665
  5. Liu W, Jin W, Zhu S, Chen Y, Liu B. Targeting regulated cell death (RCD) with small-molecule compounds in cancer therapy: a revisited review of apoptosis, autophagy-dependent cell death and necroptosis. Drug Discov Today. 2022;27(2):612-625. doi: 10.1016/j.drudis.2021.10.011
  6. Yang D, Peng D, Zhou Y, et al. Alpha-momorcharin, a type I ribosome inactivating protein, induced apoptosis of hepatocellular carcinoma SK-HEP-1 cells through mitochondrial pathway. Nat Prod Res. 2023;39(5):1128-1138. doi: 10.1080/14786419.2023.2295915
  7. Yang Y, Chen Y, Wu JH, et al. Targeting regulated cell death with plant natural compounds for cancer therapy: a revisited review of apoptosis, autophagy-dependent cell death, and necroptosis. Phytother Res. 2023;37(4):1488-1525. doi: 10.1002/ptr.7738
  8. Zeng M, Wang Y, Tao X, et al. Novel perspectives in the management of colorectal cancer: mechanistic investigations into the reversal of drug resistance via active constituents derived from herbal medicine. Phytother Res. 2024;38(12):5962-5984. doi: 10.1002/ptr.8363
  9. Zhang J, Wu Y, Li Y, et al. Natural products and derivatives for breast cancer treatment: from drug discovery to molecular mechanism. Phytomedicine. 2024;129:155600. doi: 10.1016/j.phymed.2024.155600
  10. Xu L, Xie Y, Gou Q, et al. HER2-targeted therapies for HER2-positive early-stage breast cancer: present and future. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1446414
  11. Sun Q, Mattatall GV, Vivekanantha P, et al. Magnetic resonance imaging of mammalian cells individually expressing membrane-associated magnetosome proteins I, L, B, and E. Mol Imaging. 2024;23. doi: 10.1177/15353508241289765
  12. Zhang Y, Yi S, Luan M. Advances in non-apoptotic regulated cell death: implications for malignant tumor treatment. Front Oncol. 2025;15. doi: 10.3389/fonc.2025.1519119
  13. Dou L, Fang Y, Yang H, Ai G, Shen N. Immunogenic cell death: a new strategy to enhancing cancer immunotherapy. Hum Vaccin Immunother. 2024;20(1). doi: 10.1080/21645515.2024.2437918
  14. Chen J, Wei Z, Fu K, et al. Non-apoptotic cell death in ovarian cancer: treatment, resistance and prognosis. Biomed Pharmacother. 2022;150:112929. doi: 10.1016/j.biopha.2022.112929
  15. Chen Z, Li X, Luo M, Mao W, Huang S, Zhou X. Advances in drug design strategies for phototherapy based on tumor cell death mechanisms. J Asian Nat Prod Res. 2026;28(1):1-33. doi: 10.1080/10286020.2025.2530748
  16. Wan S, Wang X, Chen W, et al. Exposure to high dose of polystyrene nanoplastics causes trophoblast cell apoptosis and induces miscarriage. Part Fibre Toxicol. 2024;21(1). doi: 10.1186/s12989-024-00574-w
  17. Unnisa A, Greig NH, Kamal MA. Inhibition of caspase 3 and caspase 9 mediated apoptosis: a multimodal therapeutic target in traumatic brain injury. Curr Neuropharmacol. 2023;21(4):1001-1012. doi: 10.2174/1570159x20666220327222921
  18. Ning Q, Liu J, Liu S, Zou Q, Li K, Li Z. TRx0237 induces apoptosis and enhances anti-PD-1 immunotherapeutic efficacy in anaplastic thyroid cancer. Int Immunopharmacol. 2025;155:114610. doi: 10.1016/j.intimp.2025.114610
  19. Lan T, He S, Luo X, et al. Disruption of NADPH homeostasis by total flavonoids from Adinandra nitida Merr. ex Li leaves triggers ROS-dependent p53 activation leading to apoptosis in non-small cell lung cancer cells. J Ethnopharmacol. 2024;332:118340. doi: 10.1016/j.jep.2024.118340
  20. Chen Y, Li X, Yang M, Liu S. Research progress on morphology and mechanism of programmed cell death. Cell Death Dis. 2024;15(5). doi: 10.1038/s41419-024-06712-8
  21. Li Y, Guo B. GSDMD-mediated pyroptosis: molecular mechanisms, diseases and therapeutic targets. Mol Biomed. 2025;6(1). doi: 10.1186/s43556-025-00249-8
  22. Broz P. Pyroptosis: molecular mechanisms and roles in disease. Cell Res. 2025;35(5):334-344. doi: 10.1038/s41422-025-01107-6
  23. Dixon SJ, Lemberg KM, Lamprecht MR, et al. Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell. 2012;149(5):1060-1072. doi: 10.1016/j.cell.2012.03.042
  24. Dong L, He J, Luo L, Wang K. Targeting the interplay of autophagy and ROS for cancer therapy: an updated overview on phytochemicals. Pharmaceuticals. 2023;16(1):92. doi: 10.3390/ph16010092
  25. Shi R, Fan H, Yu X, Tang Y, Jiang J, Liang X. Advances of podophyllotoxin and its derivatives: patterns and mechanisms. Biochem Pharmacol. 2022;200:115039. doi: 10.1016/j.bcp.2022.115039
  26. Tsvetkov P, Coy S, Petrova B, et al. Copper induces cell death by targeting lipoylated TCA cycle proteins. Science. 2022;375(6586):1254-1261. doi: 10.1126/science.abf0529
  27. Jing Z, Huang W, Mei J, et al. Advances in novel cell death mechanisms in breast cancer: intersecting perspectives on ferroptosis, cuproptosis, disulfidptosis, and pyroptosis. Mol Cancer. 2025;24(1). doi: 10.1186/s12943-025-02445-0
  28. Wang S, He H, Qu L, Shen Q, Dai Y. Dual roles of inflammatory programmed cell death in cancer: insights into pyroptosis and necroptosis. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1446486
  29. Yang F, Zhang G, An N, et al. Interplay of ferroptosis, cuproptosis, and PANoptosis in cancer treatment-induced cardiotoxicity: mechanisms and therapeutic implications. Semin Cancer Biol. 2024;106-107:106-122. doi: 10.1016/j.semcancer.2024.09.003
  30. Zhang C, Shao J, Tang X, et al. The real-world treatment characteristic and efficacy of immune checkpoint inhibitors in non-small cell lung cancer: data from a retrospective cohort study. Int Immunopharmacol. 2024;134:112152. doi: 10.1016/j.intimp.2024.112152
  31. Xiang T, Li L, Li J, et al. Chromodomain y-like (CDYL) inhibition ameliorates acute kidney injury in mice by regulating tubular pyroptosis. Acta Pharmacol Sin. 2024;45(12):2598-2610. doi: 10.1038/s41401-024-01345-1
  32. Liu Y, Li X, Sun T, Li T, Li Q. Pyroptosis in myocardial ischemia/reperfusion and its therapeutic implications. Eur J Pharmacol. 2024;971:176464. doi: 10.1016/j.ejphar.2024.176464
  33. Zhang Y, Jiao Y, Li X, et al. Pyroptosis: a new insight into eye disease therapy. Front Pharmacol. 2021;12. doi: 10.3389/fphar.2021.797110
  34. Bai Y, Pan Y, Liu X. Mechanistic insights into gasdermin-mediated pyroptosis. Nat Rev Mol Cell Biol. 2025;26(7):501-521. doi: 10.1038/s41580-025-00837-0
  35. Wang P, Ma J, Zhang R. Inflammasomes as potential therapeutic targets in atherosclerotic cardiovascular disease. EMIDDT. 2022;22(14):1378-1389. doi: 10.2174/1871530322666220407090916
  36. Lu L, Zhang Y, Tan X, et al. Emerging mechanisms of pyroptosis and its therapeutic strategy in cancer. Cell Death Discov. 2022;8(1). doi: 10.1038/s41420-022-01106-1
  37. Zhou K, Gu X, Tan H, et al. Identification pyroptosis-related gene signature to predict prognosis and associated regulation axis in colon cancer. Front Pharmacol. 2022;13. doi: 10.3389/fphar.2022.1004425
  38. Feng L, Wu Y, Yang Y, et al. QBT improved cognitive dysfunction in rats with vascular dementia by regulating the NRF2/xCT/GPX4 and NLRP3/caspase-1/GSDMD pathways to inhibit ferroptosis and pyroptosis of neurons. Int Immunopharmacol. 2024;142:113070. doi: 10.1016/j.intimp.2024.113070
  39. Zhou N, Zhang Y, Jiao Y, et al. Discovery of a novel pyroptosis inhibitor acting though modulating glutathionylation to suppress NLRP3-related signal pathway. Int Immunopharmacol. 2024;127:111314. doi: 10.1016/j.intimp.2023.111314
  40. Gao L, Dong X, Gong W, et al. Acinar cell NLRP3 inflammasome and gasdermin D (GSDMD) activation mediates pyroptosis and systemic inflammation in acute pancreatitis. Br J Pharmacol. 2021;178(17):3533-3552. doi: 10.1111/bph.15499
  41. Shi J, Zhao Y, Wang K, et al. Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death. Nature. 2015;526(7575):660-665. doi: 10.1038/nature15514
  42. Wu X, Yao J, Hu Q, et al. Emodin ameliorates acute pancreatitis-associated lung injury through inhibiting the alveolar macrophages pyroptosis. Front Pharmacol. 2022;13. doi: 10.3389/fphar.2022.873053
  43. Yang Z, Li H, Wu H, Zhou Y, Du J, Hu Z. Omega-3 polyunsaturated fatty acids alleviate hyperuricemic nephropathy by inhibiting renal pyroptosis through GPR120. Biochem Pharmacol. 2024;230:116575. doi: 10.1016/j.bcp.2024.116575
  44. He W, Wan H, Hu L, et al. Gasdermin D is an executor of pyroptosis and required for interleukin-1β secretion. Cell Res. 2015;25(12):1285-1298. doi: 10.1038/cr.2015.139
  45. He G, Chen K, Wang H, et al. Fudosteine attenuates acute lung injury in septic mice by inhibiting pyroptosis via the TXNIP/NLRP3/GSDMD pathway. Eur J Pharmacol. 2022;926:175047. doi: 10.1016/j.ejphar.2022.175047
  46. Shi J, Gao W, Shao F. Pyroptosis: gasdermin-mediated programmed necrotic cell death. Trends Biochem Sci. 2017;42(4):245-254. doi: 10.1016/j.tibs.2016.10.004
  47. Shi J, Zhao Y, Wang Y, et al. Inflammatory caspases are innate immune receptors for intracellular LPS. Nature. 2014;514(7521):187-192. doi: 10.1038/nature13683
  48. Taabazuing CY, Okondo MC, Bachovchin DA. Pyroptosis and apoptosis pathways engage in bidirectional crosstalk in monocytes and macrophages. Cell Chem Biol. 2017;24(4):507-514.e4. doi: 10.1016/j.chembiol.2017.03.009
  49. Anthony DA, Andrews DM, Watt SV, Trapani JA, Smyth MJ. Functional dissection of the granzyme family: cell death and inflammation. Immunol Rev. 2010;235(1):73-92. doi: 10.1111/j.0105-2896.2010.00907.x
  50. Zhang Z, Zhang Y, Xia S, et al. Gasdermin E suppresses tumour growth by activating anti-tumour immunity. Nature. 2020;579(7799):415-420. doi: 10.1038/s41586-020-2071-9
  51. Wang Y, Gao W, Shi X, et al. Chemotherapy drugs induce pyroptosis through caspase-3 cleavage of a gasdermin. Nature. 2017;547(7661):99-103. doi: 10.1038/nature22393
  52. Hou J, Zhao R, Xia W, et al. PD-L1-mediated gasdermin C expression switches apoptosis to pyroptosis in cancer cells and facilitates tumour necrosis. Nat Cell Biol. 2020;22(10):1264-1275. doi: 10.1038/s41556-020-0575-z
  53. Voskoboinik I, Whisstock JC, Trapani JA. Perforin and granzymes: function, dysfunction and human pathology. Nat Rev Immunol. 2015;15(6):388-400. doi: 10.1038/nri3839
  54. Zhang J, Ren Z, Hu Y, et al. High HPK1(+)PD-1(+)TIM-3(+)CD8(+) T cells infiltration predicts poor prognosis to immunotherapy in NSCLC patients. Int Immunopharmacol. 2024;127:111363. doi: 10.1016/j.intimp.2023.111363
  55. Zhou Z, He H, Wang K, et al. Granzyme A from cytotoxic lymphocytes cleaves GSDMB to trigger pyroptosis in target cells. Science. 2020;368(6494). doi: 10.1126/science.aaz7548
  56. Singh N, Baby D, Rajguru JP, Patil PB, Thakkannavar SS, Pujari VB. Inflammation and cancer. Ann Afr Med. 2019;18(3):121. doi: 10.4103/aam.aam_56_18
  57. Khandia R, Munjal A. Interplay between inflammation and cancer. Adv Protein Chem Struct Biol. 2020;119:199-245. doi: 10.1016/bs.apcsb.2019.09.004
  58. Ruan J, Wang S, Wang J. Mechanism and regulation of pyroptosis-mediated in cancer cell death. Chem Biol Interact. 2020;323:109052. doi: 10.1016/j.cbi.2020.109052
  59. Jiang M, Qi L, Li L, Li Y. The caspase-3/GSDME signal pathway as a switch between apoptosis and pyroptosis in cancer. Cell Death Discov. 2020;6(1). doi: 10.1038/s41420-020-00349-0
  60. Hou J, Hsu J, Hung M. Molecular mechanisms and functions of pyroptosis in inflammation and antitumor immunity. Mol Cell. 2021;81(22):4579-4590. doi: 10.1016/j.molcel.2021.09.003
  61. Gao H, Yao Y, Li W, et al. Caspase-6/gasdermin C-mediated tumor cell pyroptosis promotes colorectal cancer progression through CXCL2-dependent recruitment of myeloid-derived suppressor cells. Adv Sci. 2025;12(20). doi: 10.1002/advs.202411375
  62. Qiu A, Lin J, Hu H, et al. Organelles and cancer cell pyroptosis: overview and perspectives. Cell Death Dis. 2025;17(1). doi: 10.1038/s41419-025-08371-9
  63. Li Z, Mo F, Wang Y, et al. Enhancing gasdermin-induced tumor pyroptosis through preventing ESCRT-dependent cell membrane repair augments antitumor immune response. Nat Commun. 2022;13(1). doi: 10.1038/s41467-022-34036-8
  64. Fu C, Ji W, Cui Q, et al. GSDME-mediated pyroptosis promotes anti-tumor immunity of neoadjuvant chemotherapy in breast cancer. Cancer Immunol Immunother. 2024;73(9). doi: 10.1007/s00262-024-03752-z
  65. Peng X, Na R, Zhou W, et al. Nuclear translocation of gasdermin D sensitizes colorectal cancer to chemotherapy in a pyroptosis-independent manner. Oncogene. 2022;41(47):5092-5106. doi: 10.1038/s41388-022-02503-7
  66. Gagnon M, Tian S, Geyer S, et al. Distribution of clonal hematopoiesis of indeterminate potential (CHIP) is not associated with race in patients with plasma cell neoplasms. Blood Cancer J. 2022;12(7). doi: 10.1038/s41408-022-00706-5
  67. Li S, Yue M, Xu H, et al. Chemotherapeutic drugs-induced pyroptosis mediated by gasdermin E promotes the progression and chemoresistance of pancreatic cancer. Cancer Lett. 2023;564:216206. doi: 10.1016/j.canlet.2023.216206
  68. Kahaer G, Pan S, Yang C, Xie W, Lu Y. Dual function of gasdermin E: pyroptosis-mediated pan-cancer suppression versus HCC-specific oncogenic activity. Front Immunol. 2025;16. doi: 10.3389/fimmu.2025.1626311
  69. Li M, Jiang P, Yang Y, et al. The role of pyroptosis and gasdermin family in tumor progression and immune microenvironment. Exp Hematol Oncol. 2023;12(1). doi: 10.1186/s40164-023-00464-5
  70. He S, Huang Q, Cheng J. The conflicting role highlights the complexity of GSDMs in cancer. Front Immunol. 2025;16. doi: 10.3389/fimmu.2025.1531695
  71. Hou Y, Li W, Yang J, et al. Is pyroptosis a brake or an accelerator in the fate of the tumor? Cell Death Dis. 2025;16(1). doi: 10.1038/s41419-025-07866-9
  72. Hu Y, Liu Y, Zong L, et al. The multifaceted roles of GSDME-mediated pyroptosis in cancer: therapeutic strategies and persisting obstacles. Cell Death Dis. 2023;14(12). doi: 10.1038/s41419-023-06382-y
  73. Min R, Bai Y, Wang N, Liu X. Gasdermins in pyroptosis, inflammation, and cancer. Trends Mol Med. 2025;31(9):860-875. doi: 10.1016/j.molmed.2025.04.003
  74. Xu Z, Zhao Y, Zhang Y, et al. Prediction of immunotherapy response of bladder cancer with a pyroptosis-related signature indicating tumor immune microenvironment. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1387647
  75. Zhang Y, Luo M, Liao Z, et al. Pyroptosis in cancer: a dual regulator of tumor cell fate and immune activation. Cancer Biol Med. 2026:1-22. doi: 10.20892/j.issn.2095-3941.2025.0826
  76. Xi R, Cao Y, Fu N, et al. Allosteric inhibition of the tyrosine phosphatase SHP2 enhances the anti-tumor immunity of interferon α through induction of caspase-1-mediated pyroptosis in renal cancer. Int Immunopharmacol. 2024;143:113498. doi: 10.1016/j.intimp.2024.113498
  77. Hu C, Li Q, Gong S, et al. Astragaloside IV: a potential nemesis for gastric cancer. Front Pharmacol. 2025;16. doi: 10.3389/fphar.2025.1636341
  78. Xi Y, Zeng S, Tan X, Deng X. Curcumin inhibits the activity of ubiquitin ligase SMURF2 to promote NLRP3‑dependent pyroptosis in non‑small cell lung cancer cells. Int J Oncol. 2025;66(3). doi: 10.3892/ijo.2025.5727
  79. Yuan R, Zhao W, Wang Q, et al. Cucurbitacin B inhibits non-small cell lung cancer in vivo and in vitro by triggering TLR4/NLRP3/GSDMD-dependent pyroptosis. Pharmacol Res. 2021;170:105748. doi: 10.1016/j.phrs.2021.105748
  80. Chen X, Yang M, Zhang H, et al. Cucurbitacin B induces oral squamous cell carcinoma pyroptosis via GSDME and inhibits tumour growth. Transl Oncol. 2025;58:102422. doi: 10.1016/j.tranon.2025.102422
  81. Mi L, He T, Li R, et al. Cucurbitacin B in cancer: a comprehensive review of its targets and molecular mechanisms. Biochem Pharmacol. 2025;242:117240. doi: 10.1016/j.bcp.2025.117240
  82. Shi J, Tian H, Peng L, et al. A nanoplatform reshaping intracellular osmolarity and redox homeostasis against colorectal cancer. J Control Release. 2022;352:766-775. doi: 10.1016/j.jconrel.2022.10.045
  83. Gurianov DS, Antonenko SV, Telegeev GD. Nuclear localization of BCR and cortactin indicates their potential role in regulation of actin branching in nucleus. Exp Oncol. 2021;43(1):73-76. doi: 10.32471/exp-oncology.2312-8852.vol-43-no-1.15811
  84. Zhou Q, Meng Y, Li D, et al. Ferroptosis in cancer: from molecular mechanisms to therapeutic strategies. Signal Transduct Target Ther. 2024;9(1). doi: 10.1038/s41392-024-01769-5
  85. Jiang X, Stockwell BR, Conrad M. Ferroptosis: mechanisms, biology and role in disease. Nat Rev Mol Cell Biol. 2021;22(4):266-282. doi: 10.1038/s41580-020-00324-8
  86. Liu H, Yao Q, Wang X, et al. The research progress of crosstalk mechanism of autophagy and apoptosis in diabetic vascular endothelial injury. Biomed Pharmacother. 2024;170:116072. doi: 10.1016/j.biopha.2023.116072
  87. Stockwell BR. Ferroptosis turns 10: emerging mechanisms, physiological functions, and therapeutic applications. Cell. 2022;185(14):2401-2421. doi: 10.1016/j.cell.2022.06.003
  88. Zhang M, Li J, Hu W. The complex interplay between ferroptosis and atherosclerosis. Biomed Pharmacother. 2024;178:117183. doi: 10.1016/j.biopha.2024.117183
  89. Wang M, Zeng G, Xiong B, et al. ALOX5 promotes autophagy-dependent ferroptosis by activating the AMPK/mTOR pathway in melanoma. Biochem Pharmacol. 2023;212:115554. doi: 10.1016/j.bcp.2023.115554
  90. Zou Y, Li H, Graham ET, et al. Cytochrome P450 oxidoreductase contributes to phospholipid peroxidation in ferroptosis. Nat Chem Biol. 2020;16(3):302-309. doi: 10.1038/s41589-020-0472-6
  91. Ghosh MK, Mukhopadhyay M, Chatterjee IB. NADPH-initiated cytochrome P450-dependent free iron-independent microsomal lipid peroxidation: specific prevention by ascorbic acid. Mol Cell Biochem. 1997;166(1-2):35-44. doi: 10.1023/a:1006841228483
  92. Zhang Y, Xin L, Xiang M, et al. The molecular mechanisms of ferroptosis and its role in cardiovascular disease. Biomed Pharmacother. 2022;145:112423. doi: 10.1016/j.biopha.2021.112423
  93. Li J, Zhou Y, Liu J, et al. Metal-phenolic networks with ferroptosis to deliver NIR-responsive CO for synergistic therapy. J Control Release. 2022;352:313-327. doi: 10.1016/j.jconrel.2022.10.025
  94. Xie L, Fefelova N, Pamarthi SH, Gwathmey JK. Molecular mechanisms of ferroptosis and relevance to cardiovascular disease. Cells. 2022;11(17):2726. doi: 10.3390/cells11172726
  95. Costa I, Barbosa DJ, Benfeito S, et al. Molecular mechanisms of ferroptosis and their involvement in brain diseases. Pharmacol Ther. 2023;244:108373. doi: 10.1016/j.pharmthera.2023.108373
  96. Jin X, Tang J, Qiu X, et al. Ferroptosis: emerging mechanisms, biological function, and therapeutic potential in cancer and inflammation. Cell Death Discov. 2024;10(1). doi: 10.1038/s41420-024-01825-7
  97. Hsieh H, Yu M, Tseng H, Wu Y, Tsai M. Molecular mechanisms and novel therapeutics targeting ferroptosis in gastric cancer: a literature review. J Cancer. 2025;16(15):4270-4283. doi: 10.7150/jca.119757
  98. Li Z, Lu Y, Zhen Y, et al. Avicularin inhibits ferroptosis and improves cognitive impairments in Alzheimer's disease by modulating the NOX4/NRF2 axis. Phytomedicine. 2024;135:156209. doi: 10.1016/j.phymed.2024.156209
  99. Huang H, Yang G, Yang Y, Yan J, Tang X, Pan Q. TFAP2a is a novel regulator that modulates ferroptosis in gallbladder carcinoma cells via the NRF2 signalling axis. Eur Rev Med Pharmacol Sci. 2020;24(9):4745-4755. doi: 10.26355/eurrev_202005_21163
  100. Zhang S, Duan S, Xie Z, et al. Epigenetic therapeutics targeting NRF2/KEAP1 signaling in cancer oxidative stress. Front Pharmacol. 2022;13. doi: 10.3389/fphar.2022.924817
  101. Zheng X, Li H, Lin J, et al. METTL3-mediated m6A modification promotes chemoresistance of intrahepatic cholangiocarcinoma by up-regulating NRF2 to inhibit ferroptosis in cisplatin-resistant cells. J Chemother. 2024;37(7):596-606. doi: 10.1080/1120009x.2024.2421700
  102. Singh M, Arora HL, Naik R, et al. Ferroptosis in cancer: mechanism and therapeutic potential. Int J Mol Sci. 2025;26(8):3852. doi: 10.3390/ijms26083852
  103. Yapici FI, Bebber CM, von Karstedt S. A guide to ferroptosis in cancer. Mol Oncol. 2024;18(6):1378-1396. doi: 10.1002/1878-0261.13649
  104. Jiang M, Qiao M, Zhao C, Deng J, Li X, Zhou C. Targeting ferroptosis for cancer therapy: exploring novel strategies from its mechanisms and role in cancers. Transl Lung Cancer Res. 2020;9(4):1569-1584. doi: 10.21037/tlcr-20-341
  105. Zhao H, Ao L, Sorina, et al. Ferroptosis and gastric cancer: from molecular mechanisms to clinical implications. Front Immunol. 2025;16. doi: 10.3389/fimmu.2025.1581928
  106. Dou J, Liu X, Yang L, Huang D, Tan X. Ferroptosis interaction with inflammatory microenvironments: mechanism, biology, and treatment. Biomed Pharmacother. 2022;155:113711. doi: 10.1016/j.biopha.2022.113711
  107. Gao W, Tan J, Yu C. Ferroptosis in the tumor microenvironment: mechanisms, advances, and therapeutic perspectives. Front Oncol. 2025;15. doi: 10.3389/fonc.2025.1650219
  108. Shen G, Liu J, Wang Y, Deng Z, Deng F. Ferroptosis in cancer and inflammatory diseases: mechanisms and therapeutic implications. MedComm. 2025;6(9). doi: 10.1002/mco2.70349
  109. Wang J, Guo D, Jiang S, Wu W, Gao X. Targeting ferroptosis in cancer: from mechanistic insights to therapeutic approaches. Mol Biomed. 2026;7(1). doi: 10.1186/s43556-026-00416-5
  110. Mouawad N, El Jaafari N, El Sibai M, Abi-Habib RJ. Harnessing ferroptosis for cancer therapy: mechanisms and therapeutic strategies (review). Oncol Rep. 2025;55(1):1-17. doi: 10.3892/or.2025.9029
  111. Chen Q, Liu F, Zhang Y, et al. Ferroptosis in cancer toward molecular insights and clinical translation in pancreatic cancer. Mol Cancer. 2026;25(1). doi: 10.1186/s12943-025-02567-5
  112. Tang Y, Leng J, Luo Y, Luo F. Focusing on ferroptosis in alveolar bone loss during periodontitis: from mechanisms to therapies. Int Immunopharmacol. 2025;156:114683. doi: 10.1016/j.intimp.2025.114683
  113. Liu X, Zhang Y, Wu X, et al. Targeting ferroptosis pathway to combat therapy resistance and metastasis of cancer. Front Pharmacol. 2022;13. doi: 10.3389/fphar.2022.909821
  114. Li Q, Peng F, Yan X, et al. Inhibition of SLC7A11-GPX4 signal pathway is involved in aconitine-induced ferroptosis in vivo and in vitro. J Ethnopharmacol. 2023;303:116029. doi: 10.1016/j.jep.2022.116029
  115. Tang D, Chen X, Kang R, Kroemer G. Ferroptosis: molecular mechanisms and health implications. Cell Res. 2020;31(2):107-125. doi: 10.1038/s41422-020-00441-1
  116. Pourhabib Mamaghani M, Mousavikia SN, Azimian H. Ferroptosis in cancer: mechanisms, therapeutic strategies, and clinical implications. Pathol Res Pract. 2025;269:155907. doi: 10.1016/j.prp.2025.155907
  117. Li Q, Yuan H, Zhao G, et al. DDX39B protects against sorafenib-induced ferroptosis by facilitating the splicing and cytoplasmic export of GPX4 pre-mRNA in hepatocellular carcinoma. Biochem Pharmacol. 2024;225:116251. doi: 10.1016/j.bcp.2024.116251
  118. Li Y, Wang X, Chen Y, Tan Q, Liu X, Tan C. Clusterin is upregulated by erastin, a ferroptosis inducer and exerts cytoprotective effects in pancreatic adenocarcinoma cells. Anti-Cancer Drugs. 2023;35(3):227-236. doi: 10.1097/cad.0000000000001561
  119. Chen Y, Liao X, Jing P, et al. Linoleic acid-glucosamine hybrid for endogenous iron-activated ferroptosis therapy in high-grade serous ovarian cancer. Mol Pharmaceutics. 2022;19(9):3187-3198. doi: 10.1021/acs.molpharmaceut.2c00333
  120. Qin L, Zhong Y, Li Y, Yang Y. TCM targets ferroptosis: potential treatments for cancer. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1360030
  121. Yu H, Kou Q, Yuan H, et al. Alkannin triggered apoptosis and ferroptosis in gastric cancer by suppressing lipid metabolism mediated by the c-fos/SREBF1 axis. Phytomedicine. 2025;140:156604. doi: 10.1016/j.phymed.2025.156604
  122. Peng L, Hu X, Liu Z, Liu W, Huang Q, Wen Y. Therapeutic potential of resveratrol through ferroptosis modulation: insights and future directions in disease therapeutics. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1473939
  123. Mi L, Xing Z, Zhang Y, et al. Unveiling gambogenic acid as a promising antitumor compound: a review. Planta Med. 2024;90(05):353-367. doi: 10.1055/a-2258-6663
  124. Ni Y, Liu J, Zeng L, et al. Natural product manoalide promotes EGFR-TKI sensitivity of lung cancer cells by KRAS-ERK pathway and mitochondrial Ca2+ overload-induced ferroptosis. Front Pharmacol. 2023;13. doi: 10.3389/fphar.2022.1109822
  125. Liu X, Zhang Y, Gao H, et al. Induction of an MLKL mediated non-canonical necroptosis through reactive oxygen species by tanshinol A in lung cancer cells. Biochem Pharmacol. 2020;171:113684. doi: 10.1016/j.bcp.2019.113684
  126. Zhang W, Wang F, Hu C, Zhou Y, Gao H, Hu J. The progress and perspective of nanoparticle-enabled tumor metastasis treatment. Acta Pharm Sin B. 2020;10(11):2037-2053. doi: 10.1016/j.apsb.2020.07.013
  127. Su C, Xue Y, Fan S, et al. Ferroptosis and its relationship with cancer. Front Cell Dev Biol. 2025;12. doi: 10.3389/fcell.2024.1423869
  128. Zhu W, Liu X, Yang L, He Q, Huang D, Tan X. Ferroptosis and tumor immunity: in perspective of the major cell components in the tumor microenvironment. Eur J Pharmacol. 2023;961:176124. doi: 10.1016/j.ejphar.2023.176124
  129. Alu A, Han X, Ma X, Wu M, Wei Y, Wei X. The role of lysosome in regulated necrosis. Acta Pharm Sin B. 2020;10(10):1880-1903. doi: 10.1016/j.apsb.2020.07.003
  130. Lin C, Sun J, Yang Y, et al. Peptide-based nanoassembly enhances ferroptosis in cancer to overcome paclitaxel resistance. J Control Release. 2025;384:113895. doi: 10.1016/j.jconrel.2025.113895
  131. Jiang M, Liu L, Wang Z, et al. Kanglaite alleviates lung squamous cell carcinoma through ferroptosis. Int Immunopharmacol. 2025;144:113616. doi: 10.1016/j.intimp.2024.113616
  132. Mu M, Chen B, Li H, et al. Augmented the sensitivity of photothermal-ferroptosis therapy in triple-negative breast cancer through mitochondria-targeted nanoreactor. J Control Release. 2024;375:733-744. doi: 10.1016/j.jconrel.2024.09.042
  133. Deng K, Tian H, Zhang T, et al. Chemo-photothermal nanoplatform with diselenide as the key for ferroptosis in colorectal cancer. J Control Release. 2024;366:684-693. doi: 10.1016/j.jconrel.2024.01.024
  134. Peng H, Jiang Q, Mao W, et al. Fe-HCOF-PEG2000 as a hypoxia-tolerant photosensitizer to trigger ferroptosis and enhance ROS-based cancer therapy. Int J Nanomedicine. 2024;19:10165-10183. doi: 10.2147/IJN.S479848
  135. Zhang Y, Song Q, Zhang Y, et al. Iron-based nanovehicle delivering FIN56 for hyperthermia-boosted ferroptosis therapy against osteosarcoma. Int J Nanomedicine. 2024;19:91-107. doi: 10.2147/ijn.s441112
  136. Mu M, Liang X, Zhao N, et al. Boosting ferroptosis and microtubule inhibition for antitumor therapy via a carrier-free supermolecule nanoreactor. J Pharm Anal. 2023;13(1):99-109. doi: 10.1016/j.jpha.2022.09.003
  137. Wu M, Ling W, Wei J, et al. Biomimetic photosensitizer nanocrystals trigger enhanced ferroptosis for improving cancer treatment. J Control Release. 2022;352:1116-1133. doi: 10.1016/j.jconrel.2022.11.026
  138. Tian H, Zhou L, Wang Y, Nice EC, Huang C, Zhang H. A targeted nanomodulator capable of manipulating tumor microenvironment against metastasis. J Control Release. 2022;348:590-600. doi: 10.1016/j.jconrel.2022.06.022
  139. Chen L, Min J, Wang F. Copper homeostasis and cuproptosis in health and disease. Signal Transduct Target Ther. 2022;7(1):378. doi: 10.1038/s41392-022-01229-y
  140. Pan Z, Huang L, Gan Y, Xia Y, Yu W. The molecular mechanisms of cuproptosis and small-molecule drug design in diabetes mellitus. Molecules. 2024;29(12):2852. doi: 10.3390/molecules29122852
  141. Li S, Bu L, Cai L. Cuproptosis: lipoylated TCA cycle proteins-mediated novel cell death pathway. Signal Transduct Target Ther. 2022;7(1). doi: 10.1038/s41392-022-01014-x
  142. Cobine PA, Brady DC. Cuproptosis: cellular and molecular mechanisms underlying copper-induced cell death. Mol Cell. 2022;82(10):1786-1787. doi: 10.1016/j.molcel.2022.05.001
  143. Zou Y, Wu S, Xu X, et al. Cope with copper: from molecular mechanisms of cuproptosis to copper-related kidney diseases. Int Immunopharmacol. 2024;133:112075. doi: 10.1016/j.intimp.2024.112075
  144. Tang D, Chen X, Kroemer G. Cuproptosis: a copper-triggered modality of mitochondrial cell death. Cell Res. 2022;32(5):417-418. doi: 10.1038/s41422-022-00653-7
  145. Hao D, Luo W, Yan Y, Zhou J. Focus on cuproptosis: exploring new mechanisms and therapeutic application prospects of cuproptosis regulation. Biomed Pharmacother. 2024;178:117182. doi: 10.1016/j.biopha.2024.117182
  146. Xie J, Yang Y, Gao Y, He J. Cuproptosis: mechanisms and links with cancers. Mol Cancer. 2023;22(1). doi: 10.1186/s12943-023-01732-y
  147. Wang D, Tian Z, Zhang P, et al. The molecular mechanisms of cuproptosis and its relevance to cardiovascular disease. Biomed Pharmacother. 2023;163:114830. doi: 10.1016/j.biopha.2023.114830
  148. Guo Z, Chen D, Yao L, et al. The molecular mechanism and therapeutic landscape of copper and cuproptosis in cancer. Signal Transduct Target Ther. 2025;10(1). doi: 10.1038/s41392-025-02192-0
  149. Zhang T, Wang Y. Multi-omic insight into the molecular mechanism of cuproptosis-related genes in the pathogenesis of Parkinson's disease. NPJ Parkinsons Dis. 2026;12(1). doi: 10.1038/s41531-025-01250-2
  150. Li Y, Han Y, Shu Q, Kan Y, Wang Z. Cuproptosis and copper as potential mechanisms and intervention targets in Alzheimer's disease. Biomed Pharmacother. 2025;183:117814. doi: 10.1016/j.biopha.2025.117814
  151. Liu N, Chen M. Crosstalk between ferroptosis and cuproptosis: from mechanism to potential clinical application. Biomed Pharmacother. 2024;171:116115. doi: 10.1016/j.biopha.2023.116115
  152. Luo C, Wu X, Zhang S, et al. Cuproptosis: a novel therapeutic mechanism in lung cancer. Cancer Cell Int. 2025;25(1). doi: 10.1186/s12935-025-03864-1
  153. Wang Y, Zhang L, Zhou F. Cuproptosis: a new form of programmed cell death. Cell Mol Immunol. 2022;19(8):867-868. doi: 10.1038/s41423-022-00866-1
  154. Tralongo P, Ballato M, Fiorentino V, et al. Cuproptosis: a review on mechanisms, role in solid and hematological tumors, and association with viral infections. Mediterr J Hematol Infect Dis. 2025;17(1):e2025052. doi: 10.4084/mjhid.2025.052
  155. Fang X, Ji Y, Li S, et al. Paeoniflorin attenuates cuproptosis and ameliorates left ventricular remodeling after AMI in hypobaric hypoxia environments. J Nat Med. 2024;78(3):664-676. doi: 10.1007/s11418-024-01781-7
  156. Wang Q, Chen H, Lv Z, et al. The molecular mechanism of cuproptosis and research progress in pancreatic diseases. Ann Med. 2025;58(1). doi: 10.1080/07853890.2025.2608490
  157. Zhang X, Peng Z, Wang Q, Zhang W, Bu Q, Sun D. Copper oxide nanoparticles induce pulmonary inflammation via triggering cellular cuproptosis. Toxicology. 2025;514:154131. doi: 10.1016/j.tox.2025.154131
  158. Tang D, Kroemer G, Kang R. Targeting cuproplasia and cuproptosis in cancer. Nat Rev Clin Oncol. 2024;21(5):370-388. doi: 10.1038/s41571-024-00876-0
  159. Zhang P, Yang H, Zhu K, et al. SLC31A1 identifying a novel biomarker with potential prognostic and immunotherapeutic potential in pan-cancer. Biomedicines. 2023;11(11):2884. doi: 10.3390/biomedicines11112884
  160. Jiang D, Zhuang L, Koong AC, Gan B. Cuproptosis in cancer: from molecular mechanisms to therapeutic intervention. Trends Cancer. 2026;12(3):275-286. doi: 10.1016/j.trecan.2025.12.002
  161. Huang X, Shen J, Huang K, Wang L, Sethi G, Ma Z. Cuproptosis in cancers: function and implications from bench to bedside. Biomed Pharmacother. 2024;176:116874. doi: 10.1016/j.biopha.2024.116874
  162. Springer C, Humayun D, Skouta R. Cuproptosis: unraveling the mechanisms of copper-induced cell death and its implication in cancer therapy. Cancers. 2024;16(3):647. doi: 10.3390/cancers16030647
  163. Hu J, Zhu J, Chen T, Zhao Y, Xu Q, Wang Y. Cuproptosis in cancer therapy: mechanisms, therapeutic application and future prospects. J Mater Chem B. 2024;12(47):12191-12206. doi: 10.1039/d4tb01877j
  164. Mao L, Lu J, Wen X, et al. Cuproptosis: mechanisms and nanotherapeutic strategies in cancer and beyond. Chem Soc Rev. 2025;54(13):6282-6334. doi: 10.1039/d5cs00083a
  165. Cong Y, Li N, Zhang Z, Shang Y, Zhao H. Cuproptosis: molecular mechanisms, cancer prognosis, and therapeutic applications. J Transl Med. 2025;23(1). doi: 10.1186/s12967-025-06121-1
  166. Qin W, Sheng H, Hu X, Burden RE, Martin SL, Wu H. Cuproptosis in cancer: emerging mechanism and therapeutic opportunities. Trends Pharmacol Sci. 2026;47(4):386-402. doi: 10.1016/j.tips.2026.02.004
  167. Wang Y, Chen Y, Zhang J, et al. Cuproptosis: a novel therapeutic target for overcoming cancer drug resistance. Drug Resist Updat. 2024;72:101018. doi: 10.1016/j.drup.2023.101018
  168. Zhang C, Huang T, Li L. Targeting cuproptosis for cancer therapy: mechanistic insights and clinical perspectives. J Hematol Oncol. 2024;17(1). doi: 10.1186/s13045-024-01589-8
  169. Wu T, Wang S, Liu Y, Bai X, Shi C. Roles and mechanisms of cuproptosis for reversing cancer therapeutic resistance. Int J Pharm. 2025;685:126267. doi: 10.1016/j.ijpharm.2025.126267
  170. Hao Q, Gan Y, Zhou X. Tackling cuproptosis: from metabolic rewiring to therapeutic exploitation in cancer. Cell Mol Immunol. 2026;23(3):239-260. doi: 10.1038/s41423-026-01387-x
  171. Boaru DL, Leon-Oliva DD, Castro-Martinez PD, et al. Cuproptosis: current insights into its multifaceted role in disease, cancer, and translational/therapeutic opportunities. Biomed Pharmacother. 2025;190:118422. doi: 10.1016/j.biopha.2025.118422
  172. Chen S, Zhang S, Yuan Y, et al. Prognostic value of cuproptosis-related genes signature and its impact on the reshaped immune microenvironment of glioma. Front Pharmacol. 2022;13. doi: 10.3389/fphar.2022.1016520
  173. Liu T, Zhou Z, Zhang M, et al. Cuproptosis-immunotherapy using PD-1 overexpressing T cell membrane-coated nanosheets efficiently treats tumor. J Control Release. 2023;362:502-512. doi: 10.1016/j.jconrel.2023.08.055
  174. Guo K, Ren S, Zhang H, et al. Biomimetic gold nanorods modified with erythrocyte membranes for imaging-guided photothermal/gene synergistic therapy. ACS Appl Mater Interfaces. 2023;15(21):25285-25299. doi: 10.1021/acsami.3c00865
  175. Feng Q, Huo C, Wang M, Huang H, Zheng X, Xie M. Research progress on cuproptosis in cancer. Front Pharmacol. 2024;15. doi: 10.3389/fphar.2024.1290592
  176. Du O, Yan Y, Yang H, et al. ALPK1 signaling pathway activation by HMGB1 drives microglial pyroptosis and ferroptosis and brain injury after acute ischemic stroke. Int Immunopharmacol. 2025;149:114229. doi: 10.1016/j.intimp.2025.114229
  177. Beltrán-Visiedo M, Soler-Agesta R, Sarosiek KA, Green DR, Galluzzi L. Regulation of inflammatory processes by caspases. Nat Rev Mol Cell Biol. 2025;26(11):884-901. doi: 10.1038/s41580-025-00869-6
  178. Liu X, Luo Q, Zhao Y, Ren P, Jin Y, Zhou J. The ferroptosis-mitochondrial axis in depression: unraveling the feedforward loop of oxidative stress, metabolic homeostasis dysregulation, and neuroinflammation. Antioxidants. 2025;14(5):613. doi: 10.3390/antiox14050613
  179. Zhou B, Zhang J, Liu X, et al. Tom20 senses iron-activated ROS signaling to promote melanoma cell pyroptosis. Cell Res. 2018;28(12):1171-1185. doi: 10.1038/s41422-018-0090-y
  180. Wang Z, Hu X, Cui P, et al. Progress in understanding the role of cGAS-STING pathway associated with programmed cell death in intervertebral disc degeneration. Cell Death Discov. 2023;9(1). doi: 10.1038/s41420-023-01607-7
  181. Chen Y, Fang Z, Yi X, Wei X, Jiang D. The interaction between ferroptosis and inflammatory signaling pathways. Cell Death Dis. 2023;14(3). doi: 10.1038/s41419-023-05716-0
  182. Wang H, Shu L, Lv C, et al. BRCC36 deubiquitinates HMGCR to regulate the interplay between ferroptosis and pyroptosis. Adv Sci. 2024;11(11). doi: 10.1002/advs.202304263
  183. Gao M, Yi J, Zhu J, Minikes AM, et al. Role of mitochondria in ferroptosis. Mol Cell. 2019;73(2):354-363.e3. doi: 10.1016/j.molcel.2018.10.042
  184. Badgley MA, Kremer DM, Maurer HC, et al. Cysteine depletion induces pancreatic tumor ferroptosis in mice. Science. 2020;368(6486):85-89. doi: 10.1126/science.aaw9872
  185. Wang W, Lu K, Jiang X, et al. Ferroptosis inducers enhanced cuproptosis induced by copper ionophores in primary liver cancer. J Exp Clin Cancer Res. 2023;42(1). doi: 10.1186/s13046-023-02720-2
  186. Zhou X, Peng S. The cross-talk and interplay between ferroptosis and cuproptosis in tumor and therapeutics. Cell Oncol. 2026;49(1). doi: 10.1007/s13402-025-01138-6
  187. Xiong C, Ling H, Hao Q, Zhou X. Cuproptosis: p53-regulated metabolic cell death? Cell Death Differ. 2023;30(4):876-884. doi: 10.1038/s41418-023-01125-0
  188. Guo H, Ouyang Y, Yin H, et al. Induction of autophagy via the ROS-dependent AMPK-mTOR pathway protects copper-induced spermatogenesis disorder. Redox Biol. 2022;49:102227. doi: 10.1016/j.redox.2021.102227
  189. Qiao L, Zhu G, Jiang T, et al. Self-destructive copper carriers induce pyroptosis and cuproptosis for efficient tumor immunotherapy against dormant and recurrent tumors. Adv Mater. 2023;36(8). doi: 10.1002/adma.202308241
  190. Zhang L, Zhao L, Lin X, et al. Comparison of tumor non-specific and PD-L1 specific imaging by near-infrared fluorescence/Cherenkov luminescence dual-modality in-situ imaging. Mol Imaging. 2024;23. doi: 10.1177/15353508241261473
  191. Wang Y, Zhao H, Sun K, et al. Conductive coordination nanozyme prodrugs precisely trigger pyroptosis, cuproptosis and ferroptosis for in situ cancer vaccination. Signal Transduct Target Ther. 2026;11(1). doi: 10.1038/s41392-026-02607-6
  192. Chauhan P, Pandey P, Singh A, et al. Exploring the synergetic role of cuproptosis and ferroptosis and their implication in advancing cancer therapeutics. Discov Oncol. 2025;16(1). doi: 10.1007/s12672-025-03150-6
Share
Back to top
Eurasian Journal of Medicine and Oncology, Electronic ISSN: 2587-196X Print ISSN: 2587-2400, Published by AccScience Publishing