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靶向程序性细胞死亡:细胞凋亡、坏死性凋亡、焦亡、铁死亡和铜死亡在抗癌免疫中的作用

Targeting regulated cell death: Apoptosis, necroptosis, pyroptosis, ferroptosis, and cuproptosis in anticancer immunity.

作者信息

Guo Ziyu, Liu Yihuang, Chen Danyao, Sun Yuming, Li Daishi, Meng Yu, Zhou Qian, Zeng Furong, Deng Guangtong, Chen Xiang

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.

National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology, Changsha 410008, Hunan Province, China.

出版信息

J Transl Int Med. 2025 Mar 19;13(1):10-32. doi: 10.1515/jtim-2025-0004. eCollection 2025 Feb.

DOI:10.1515/jtim-2025-0004
PMID:40115032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11921819/
Abstract

In the evolving landscape of cancer treatment, the strategic manipulation of regulated cell death (RCD) pathways has emerged as a crucial component of effective anti-tumor immunity. Evidence suggests that tumor cells undergoing RCD can modify the immunogenicity of the tumor microenvironment (TME), potentially enhancing its ability to suppress cancer progression and metastasis. In this review, we first explore the mechanisms of apoptosis, necroptosis, pyroptosis, ferroptosis, and cuproptosis, along with the crosstalk between these cell death modalities. We then discuss how these processes activate antigen-presenting cells, facilitate the cross-priming of CD8+ T cells, and trigger anti-tumor immune responses, highlighting the complex effects of novel forms of tumor cell death on TME and tumor biology. Furthermore, we summarize potential drugs and nanoparticles that can induce or inhibit these emerging RCD pathways and their therapeutic roles in cancer treatment. Finally, we put forward existing challenges and future prospects for targeting RCD in anti-cancer immunity. Overall, this review enhances our understanding of the molecular mechanisms and biological impacts of RCD-based therapies, providing new perspectives and strategies for cancer treatment.

摘要

在不断演变的癌症治疗格局中,对程序性细胞死亡(RCD)途径的策略性调控已成为有效抗肿瘤免疫的关键组成部分。有证据表明,经历RCD的肿瘤细胞可改变肿瘤微环境(TME)的免疫原性,这可能增强其抑制癌症进展和转移的能力。在本综述中,我们首先探讨凋亡、坏死性凋亡、炎性小体介导的细胞焦亡、铁死亡和铜死亡的机制,以及这些细胞死亡方式之间的相互作用。然后,我们讨论这些过程如何激活抗原呈递细胞,促进CD8 + T细胞的交叉呈递,并触发抗肿瘤免疫反应,强调新型肿瘤细胞死亡形式对TME和肿瘤生物学的复杂影响。此外,我们总结了能够诱导或抑制这些新兴RCD途径的潜在药物和纳米颗粒及其在癌症治疗中的治疗作用。最后,我们提出了在抗癌免疫中靶向RCD的现有挑战和未来前景。总的来说,本综述增进了我们对基于RCD的治疗的分子机制和生物学影响的理解,为癌症治疗提供了新的视角和策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/f44a37a595fc/j_jtim-2025-0004_fig_005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/a4d3791e8ab0/j_jtim-2025-0004_fig_001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/de58e9d1200d/j_jtim-2025-0004_fig_002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/b4f6f46f812e/j_jtim-2025-0004_fig_003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/719c3ab51a0c/j_jtim-2025-0004_fig_004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/f44a37a595fc/j_jtim-2025-0004_fig_005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/a4d3791e8ab0/j_jtim-2025-0004_fig_001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/de58e9d1200d/j_jtim-2025-0004_fig_002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/b4f6f46f812e/j_jtim-2025-0004_fig_003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/719c3ab51a0c/j_jtim-2025-0004_fig_004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06eb/11921819/f44a37a595fc/j_jtim-2025-0004_fig_005.jpg

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