Hang Zi-Shan, Huang Yue-Ying, Song An, Sun Zhi-Jun
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Frontier Science Center for Immunology and Metabolism, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan, China.
The Affiliated Stomatological Hospital, State Key Laboratory Cultivation Base of Research, Prevention and Treatment of Oral Diseases, Jiangsu Province Engineering Research Center of Stomatological Translational Medicine, Nanjing Medical University, Nanjing, China.
Int J Med Sci. 2025 Jul 11;22(13):3277-3291. doi: 10.7150/ijms.109515. eCollection 2025.
Radiotherapy, one of the most utilized strategies to combat malignancies, has been constantly explored for its effectiveness and optimized, and it is currently operating at the molecular level. The tumor microenvironment (TME), where complicated changes take place under radiotherapy and other treatments, inevitably draws our attention to metabolic alterations, immunogenic cell death (ICD) and immunological interactions. In response to radiotherapy, tumor metabolism promotes DNA and membrane repair processes and reduces oxidative stress, thereby collectively alleviating the occurrence of cell death. Moreover, the induction of pyroptosis, necroptosis and ferroptosis under radiotherapy has the potential to increase antitumor immunity. Therefore, comprehensive knowledge about how radiotherapy triggers these modalities of ICD mechanically is necessary for developing nanomedicines with more accurate targets. In addition, information on clinical advancements as well as the management of adverse events is important for investigating radiotherapy combined with immunotherapy. This review provides an overview of up-to-date findings on metabolic changes and ICD under radiotherapy and provides insight into the status of the TME.
放射疗法是对抗恶性肿瘤最常用的策略之一,人们一直在不断探索其有效性并进行优化,目前已深入到分子层面。肿瘤微环境(TME)在放疗和其他治疗过程中会发生复杂变化,不可避免地引起了我们对代谢改变、免疫原性细胞死亡(ICD)和免疫相互作用的关注。放疗后,肿瘤代谢会促进DNA和细胞膜修复过程,并减轻氧化应激,从而共同减轻细胞死亡的发生。此外,放疗诱导的细胞焦亡、坏死性凋亡和铁死亡有可能增强抗肿瘤免疫力。因此,全面了解放疗如何机械性地触发这些ICD模式对于开发具有更精确靶点的纳米药物至关重要。此外,有关临床进展以及不良事件管理的信息对于研究放疗联合免疫疗法也很重要。本综述概述了放疗后代谢变化和ICD的最新研究结果,并深入探讨了TME的现状。
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