Wang Tianxiang, Zhou Xuemei, Yin Xinhao, Zhang Axue, Fan Yaxuan, Chen Kun, Tao Haojun, Tang Zhongxin, Zhang Pingchuan, He Xia, Yin Li
Department of Radiation Oncology, The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing, Jiangsu 210009, P.R. China.
Int J Oncol. 2025 Sep;67(3). doi: 10.3892/ijo.2025.5781. Epub 2025 Aug 8.
Ferroptosis is an iron‑dependent, lipid peroxidation‑driven form of regulated immunogenic cell death (ICD). ICD has demonstrated potential to overcome resistance to conventional cancer therapies, enhancing the efficacy of treatments such as chemotherapy, radiotherapy, immunotherapy and photodynamic therapy. Notably, in the context of radiotherapy, ferroptosis serves a key role, particularly when combined with radioimmunotherapy. Mitochondria are central to the regulation of radiation‑induced oxidative stress and the remodeling of the immune microenvironment, and they undergo characteristic morphological changes during the ferroptotic process. However, the precise regulatory association between mitochondrial dysfunction and ferroptosis remains incompletely understood, and there is an ongoing debate regarding this complex interaction. The present review aimed to explore the mechanisms through which mitochondria and ferroptosis interact in the context of radiotherapy, with a focus on how ferroptosis exacerbates mitochondrial dysfunction. Additionally, the present review proposed novel strategies leveraging radioimmunotherapy to offer more precise and effective approaches for cancer treatment.
铁死亡是一种铁依赖性、由脂质过氧化驱动的程序性免疫原性细胞死亡(ICD)形式。ICD已显示出克服对传统癌症疗法耐药性的潜力,可增强化疗、放疗、免疫疗法和光动力疗法等治疗的疗效。值得注意的是,在放疗背景下,铁死亡起着关键作用,尤其是与放射免疫疗法联合使用时。线粒体对于辐射诱导的氧化应激调节和免疫微环境重塑至关重要,并且它们在铁死亡过程中会发生特征性的形态变化。然而,线粒体功能障碍与铁死亡之间的确切调节关联仍未完全明确,关于这种复杂相互作用的争论仍在继续。本综述旨在探讨放疗背景下线粒体与铁死亡相互作用的机制,重点关注铁死亡如何加剧线粒体功能障碍。此外,本综述提出了利用放射免疫疗法的新策略,为癌症治疗提供更精确有效的方法。
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