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纳米医学靶向铁死亡以克服抗癌治疗耐药性。

Nanomedicine targeting ferroptosis to overcome anticancer therapeutic resistance.

机构信息

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Medical Research Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.

Nanhai Translational Innovation Center of Precision Immunology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Foshan, 528200, China.

出版信息

Sci China Life Sci. 2024 Jan;67(1):19-40. doi: 10.1007/s11427-022-2340-4. Epub 2023 Sep 15.

DOI:10.1007/s11427-022-2340-4
PMID:37728804
Abstract

A potential reason for the failure of tumor therapies is treatment resistance. Resistance to chemotherapy, radiotherapy, and immunotherapy continues to be a major obstacle in clinic, resulting in tumor recurrence and metastasis. The major mechanisms of therapy resistance are inhibitions of cell deaths, like apoptosis and necrosis, through drug inactivation and excretion, repair of DNA damage, tumor heterogeneity, or changes in tumor microenvironment, etc. Recent studies have shown that ferroptosis play a major role in therapies resistance by inducing phospholipid peroxidation and iron-dependent cell death. Some ferroptosis inducers in combination with clinical treatment techniques have been used to enhance the effect in tumor therapy. Notably, versatile ferroptosis nanoinducers exhibit an extensive range of functions in reversing therapy resistance, including directly triggering ferroptosis and feedback regulation. Herein, we provide a detailed description of the design, mechanism, and therapeutic application of ferroptosis-mediated synergistic tumor therapeutics. We also discuss the prospect and challenge of nanomedicine in tumor therapy resistance by regulating ferroptosis and combination therapy.

摘要

肿瘤治疗失败的一个潜在原因是治疗耐药性。化疗、放疗和免疫治疗的耐药性仍然是临床的主要障碍,导致肿瘤复发和转移。治疗耐药性的主要机制包括通过药物失活和排泄、DNA 损伤修复、肿瘤异质性或肿瘤微环境改变等来抑制细胞死亡,如细胞凋亡和坏死。最近的研究表明,铁死亡通过诱导磷脂过氧化和铁依赖性细胞死亡在治疗耐药性中起主要作用。一些铁死亡诱导剂与临床治疗技术联合使用,以增强肿瘤治疗效果。值得注意的是,多功能铁死亡纳米诱导剂在逆转治疗耐药性方面表现出广泛的功能,包括直接触发铁死亡和反馈调节。本文详细描述了铁死亡介导的协同肿瘤治疗的设计、机制和治疗应用。我们还讨论了通过调节铁死亡和联合治疗,纳米医学在肿瘤治疗耐药性方面的前景和挑战。

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Nanomedicine targeting ferroptosis to overcome anticancer therapeutic resistance.纳米医学靶向铁死亡以克服抗癌治疗耐药性。
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本文引用的文献

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Nanomedicine-mediated ferroptosis targeting strategies for synergistic cancer therapy.纳米医学介导的铁死亡靶向策略用于协同癌症治疗。
J Mater Chem B. 2023 Feb 8;11(6):1171-1190. doi: 10.1039/d2tb02161g.
2
Radiotherapy-mediated redox homeostasis-controllable nanomedicine for enhanced ferroptosis sensitivity in tumor therapy.放射治疗介导的氧化还原平衡控制纳米医学增强肿瘤治疗中的铁死亡敏感性。
Acta Biomater. 2023 Mar 15;159:300-311. doi: 10.1016/j.actbio.2023.01.022. Epub 2023 Jan 13.
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Non-apoptotic cell death-based cancer therapy: Molecular mechanism, pharmacological modulators, and nanomedicine.
从线粒体失调到铁死亡:探索放射免疫疗法的新策略与挑战(综述)
Int J Oncol. 2025 Sep;67(3). doi: 10.3892/ijo.2025.5781. Epub 2025 Aug 8.
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Inhibition of recurrence and metastasis in triple-negative breast cancer through nanoparticle-mediated silencing of LPCAT1 to remodel ATP energy metabolism.通过纳米颗粒介导沉默LPCAT1以重塑ATP能量代谢来抑制三阴性乳腺癌的复发和转移。
Sci China Life Sci. 2025 May 7. doi: 10.1007/s11427-024-2887-x.
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STAT1 increases the sensitivity of lung adenocarcinoma to carbon ion irradiation via HO-1-mediated ferroptosis.信号转导及转录激活因子1(STAT1)通过血红素加氧酶-1(HO-1)介导的铁死亡增加肺腺癌对碳离子辐射的敏感性。
Mol Cell Biochem. 2025 Mar 14. doi: 10.1007/s11010-025-05240-z.
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Isowalsuranolide targets TrxR1/2 and triggers lysosomal biogenesis and autophagy via the p53-TFEB/TFE3 axis.异沃苏烷内酯靶向硫氧还蛋白还原酶1/2,并通过p53-转录因子EB/转录因子E3轴触发溶酶体生物发生和自噬。
Sci China Life Sci. 2025 Mar 7. doi: 10.1007/s11427-023-2563-6.
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Int J Nanomedicine. 2024 Oct 7;19:10165-10183. doi: 10.2147/IJN.S479848. eCollection 2024.
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