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细胞死亡塑造癌症免疫:聚焦 PANoptosis。

Cell death shapes cancer immunity: spotlighting PANoptosis.

机构信息

National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, College of Pharmacy, Chongqing University of Arts and Sciences, Chongqing, 402160, People's Republic of China.

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, 30322, USA.

出版信息

J Exp Clin Cancer Res. 2024 Jun 15;43(1):168. doi: 10.1186/s13046-024-03089-6.

DOI:10.1186/s13046-024-03089-6
PMID:38877579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11179218/
Abstract

PANoptosis represents a novel type of programmed cell death (PCD) with distinctive features that incorporate elements of pyroptosis, apoptosis, and necroptosis. PANoptosis is governed by a newly discovered cytoplasmic multimeric protein complex known as the PANoptosome. Unlike each of these PCD types individually, PANoptosis is still in the early stages of research and warrants further exploration of its specific regulatory mechanisms and primary targets. In this review, we provide a brief overview of the conceptual framework and molecular components of PANoptosis. In addition, we highlight recent advances in the understanding of the molecular mechanisms and therapeutic applications of PANoptosis. By elucidating the complex crosstalk between pyroptosis, apoptosis and necroptosis and summarizing the functional consequences of PANoptosis with a special focus on the tumor immune microenvironment, this review aims to provide a theoretical basis for the potential application of PANoptosis in cancer therapy.

摘要

细胞焦亡样程序性细胞死亡(PANoptosis)是一种新型的程序性细胞死亡(PCD),具有独特的特征,融合了细胞焦亡、细胞凋亡和细胞坏死的特征。PANoptosis 受一种新发现的细胞质多聚体蛋白复合物调控,称为 PANoptosome。与每种单独的 PCD 类型不同,PANoptosis 仍处于研究的早期阶段,需要进一步探索其特定的调节机制和主要靶点。在这篇综述中,我们简要概述了 PANoptosis 的概念框架和分子组成。此外,我们还强调了对 PANoptosis 的分子机制和治疗应用的理解的最新进展。通过阐明细胞焦亡、细胞凋亡和细胞坏死之间的复杂串扰,并总结 PANoptosis 的功能后果,特别关注肿瘤免疫微环境,本综述旨在为 PANoptosis 在癌症治疗中的潜在应用提供理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/2ede5d753989/13046_2024_3089_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/9dc7cf286a3f/13046_2024_3089_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/f0622073f62b/13046_2024_3089_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/c9c8927ab8b3/13046_2024_3089_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/2ede5d753989/13046_2024_3089_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/9dc7cf286a3f/13046_2024_3089_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/f0622073f62b/13046_2024_3089_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/c9c8927ab8b3/13046_2024_3089_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b98/11179218/2ede5d753989/13046_2024_3089_Fig4_HTML.jpg

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本文引用的文献

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Circadian tumor infiltration and function of CD8 T cells dictate immunotherapy efficacy.昼夜节律性肿瘤浸润和 CD8 T 细胞功能决定免疫治疗效果。
Cell. 2024 May 23;187(11):2690-2702.e17. doi: 10.1016/j.cell.2024.04.015. Epub 2024 May 8.
2
Inflammatory cell death PANoptosis is induced by the anti-cancer curaxin CBL0137 via eliciting the assembly of ZBP1-associated PANoptosome.炎性细胞死亡 PANoptosis 是由抗癌药物 curaxin CBL0137 通过引发 ZBP1 相关 PANoptosome 的组装而诱导的。
Inflamm Res. 2024 Apr;73(4):597-617. doi: 10.1007/s00011-024-01858-9. Epub 2024 Feb 14.
3
Sodium sulfite triggered hepatic apoptosis, necroptosis, and pyroptosis by inducing mitochondrial damage in mice and AML-12 cells.
A potential strategy to rebuild the tumor immune microenvironment: PANoptosis.
重建肿瘤免疫微环境的一种潜在策略:全凋亡。
Front Immunol. 2025 Aug 4;16:1626411. doi: 10.3389/fimmu.2025.1626411. eCollection 2025.
4
Diverse functions of NLRP3 inflammasome in PANoptosis and diseases.NLRP3炎性小体在PAN细胞焦亡及疾病中的多种功能
Cell Death Discov. 2025 Aug 19;11(1):389. doi: 10.1038/s41420-025-02689-1.
5
Single-Cell RNA Sequencing Integrated with Bulk-RNA Sequencing Analysis Reveals Prognostic Signatures Based on PANoptosis in Hepatocellular Carcinoma.单细胞RNA测序与批量RNA测序分析相结合揭示基于肝细胞癌PAN凋亡的预后特征
J Hepatocell Carcinoma. 2025 Jul 29;12:1661-1676. doi: 10.2147/JHC.S533777. eCollection 2025.
6
Comprehensive landscape of cell death mechanisms: from molecular cross-talk to therapeutic innovation in oncology.细胞死亡机制全景:从分子相互作用到肿瘤学治疗创新
Front Cell Dev Biol. 2025 Jul 16;13:1611055. doi: 10.3389/fcell.2025.1611055. eCollection 2025.
7
PANoptosis in cancer: bridging molecular mechanisms to therapeutic innovations.癌症中的全程序死亡:将分子机制与治疗创新相联系
Cell Mol Immunol. 2025 Jul 28. doi: 10.1038/s41423-025-01329-z.
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AIM2-PANoptosome-driven PANoptosis in hepatic lipid dysregulation induced by β-HCH and nanoplastics co-exposure.AIM2-泛凋亡小体驱动的泛凋亡在β-六氯环己烷与纳米塑料共同暴露诱导的肝脏脂质失调中的作用
Apoptosis. 2025 Jul 23. doi: 10.1007/s10495-025-02147-4.
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The role of lipid metabolism imbalance in copper-induced PANoptosis in broiler kidney.脂质代谢失衡在铜诱导的肉鸡肾脏PANoptosis中的作用。
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亚硫酸钠通过诱导小鼠和 AML-12 细胞线粒体损伤引发肝细胞凋亡、坏死性凋亡和焦亡。
J Hazard Mater. 2024 Apr 5;467:133719. doi: 10.1016/j.jhazmat.2024.133719. Epub 2024 Feb 6.
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Integrated NLRP3, AIM2, NLRC4, Pyrin inflammasome activation and assembly drive PANoptosis.NLRP3、AIM2、NLRC4、Pyrin 炎症小体激活和组装导致全凋亡。
Cell Mol Immunol. 2023 Dec;20(12):1513-1526. doi: 10.1038/s41423-023-01107-9. Epub 2023 Nov 27.
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Tumor-associated neutrophils upregulate PANoptosis to foster an immunosuppressive microenvironment of non-small cell lung cancer.肿瘤相关中性粒细胞上调 PANoptosis 以促进非小细胞肺癌的免疫抑制微环境。
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Biomed Pharmacother. 2023 Dec;168:115696. doi: 10.1016/j.biopha.2023.115696. Epub 2023 Oct 12.
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Immunogenic PANoptosis-Initiated Cancer Sono-Immune Reediting Nanotherapy by Iteratively Boosting Cancer Immunity Cycle.免疫原性 PANoptosis 引发的癌症声免疫再编辑纳米治疗通过迭代增强癌症免疫循环。
Adv Mater. 2024 Jan;36(2):e2305361. doi: 10.1002/adma.202305361. Epub 2023 Nov 23.
9
Expression patterns and immunological characterization of PANoptosis -related genes in gastric cancer.胃癌中 PANoptosis 相关基因的表达模式和免疫学特征。
Front Endocrinol (Lausanne). 2023 Aug 18;14:1222072. doi: 10.3389/fendo.2023.1222072. eCollection 2023.
10
Immune regulator IRF1 contributes to ZBP1-, AIM2-, RIPK1-, and NLRP12-PANoptosome activation and inflammatory cell death (PANoptosis).免疫调节因子 IRF1 有助于 ZBP1、AIM2、RIPK1 和 NLRP12 形成 PANoptosome 并激活炎症细胞死亡(PANoptosis)。
J Biol Chem. 2023 Sep;299(9):105141. doi: 10.1016/j.jbc.2023.105141. Epub 2023 Aug 7.