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细胞焦亡在炎症性疾病和癌症中的作用。

Pyroptosis in inflammatory diseases and cancer.

机构信息

Engineering Research Center of Molecular & Neuroimaging, Ministry of Education, School of Life Science and Technology, Xidian University, Xi'an, Shaanxi, 710126, P. R. China.

Department of Radiotherapy, Chinese PLA General Hospital, Beijing, 100071, P. R. China.

出版信息

Theranostics. 2022 May 16;12(9):4310-4329. doi: 10.7150/thno.71086. eCollection 2022.


DOI:10.7150/thno.71086
PMID:35673561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9169370/
Abstract

Pyroptosis is a lytic and inflammatory type of programmed cell death that is usually triggered by inflammasomes and executed by gasdermin proteins. The main characteristics of pyroptosis are cell swelling, membrane perforation, and the release of cell contents. In normal physiology, pyroptosis plays a critical role in host defense against pathogen infection. However, excessive pyroptosis may cause immoderate and continuous inflammatory responses that involves in the occurrence of inflammatory diseases. Attractively, as immunogenic cell death, pyroptosis can serve as a new strategy for cancer elimination by inducing pyroptotic cell death and activating intensely antitumor immunity. To make good use of this double-edged sword, the molecular mechanisms, and therapeutic implications of pyroptosis in related diseases need to be fully elucidated. In this review, we first systematically summarize the signaling pathways of pyroptosis and then present the available evidences indicating the role of pyroptosis in inflammatory diseases and cancer. Based on this, we focus on the recent progress in strategies that inhibit pyroptosis for treatment of inflammatory diseases, and those that induce pyroptosis for cancer therapy. Overall, this should shed light on future directions and provide novel ideas for using pyroptosis as a powerful tool to fight inflammatory diseases and cancer.

摘要

细胞焦亡是一种由炎性小体激活、并由Gasdermin 蛋白执行的溶酶体依赖性的细胞程序性死亡方式。细胞焦亡的主要特征是细胞肿胀、细胞膜穿孔以及细胞内容物的释放。在正常生理条件下,细胞焦亡在宿主防御病原体感染中发挥着至关重要的作用。然而,过度的细胞焦亡可能导致过度和持续的炎症反应,从而涉及炎症性疾病的发生。引人注目的是,作为一种免疫原性细胞死亡,细胞焦亡可以通过诱导细胞焦亡和激活强烈的抗肿瘤免疫来作为消除肿瘤的新策略。为了充分利用这把双刃剑,需要充分阐明细胞焦亡在相关疾病中的分子机制和治疗意义。在这篇综述中,我们首先系统地总结了细胞焦亡的信号通路,然后介绍了表明细胞焦亡在炎症性疾病和癌症中发挥作用的现有证据。在此基础上,我们重点介绍了抑制细胞焦亡治疗炎症性疾病和诱导细胞焦亡治疗癌症的最新进展。总的来说,这将为未来的研究方向提供启示,并为将细胞焦亡作为一种强大的工具用于治疗炎症性疾病和癌症提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/c062aab59c63/thnov12p4310g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/b67b06005416/thnov12p4310g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/c75ce10ae5d7/thnov12p4310g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/71bf87862805/thnov12p4310g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/dca49fb63b4d/thnov12p4310g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/79f37d1a18b8/thnov12p4310g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/ffcfa18cc0ca/thnov12p4310g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/c062aab59c63/thnov12p4310g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/b67b06005416/thnov12p4310g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/c75ce10ae5d7/thnov12p4310g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/71bf87862805/thnov12p4310g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/dca49fb63b4d/thnov12p4310g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/79f37d1a18b8/thnov12p4310g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/ffcfa18cc0ca/thnov12p4310g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c42/9169370/c062aab59c63/thnov12p4310g007.jpg

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引用本文的文献

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Long non-coding RNA STMN1P2 promotes breast cancer doxorubicin resistance by inhibiting pyroptosis through the hnRNPU-EZH2-TARF6-MALT1-caspase-1 pathway.

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[2]
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[3]
Integrating Spatial Multi-Omics and Machine Learning to Unravel the Role of PANoptosis in Bladder Cancer Prognosis and Immunotherapy Response.

Oncol Res. 2025-8-28

[4]
Circ_0070987 Promotes Pyroptosis of Ovarian Granulosa Cells in Polycystic Ovarian Syndrome Through the miR-139-5/CDH1 Axis.

Reprod Sci. 2025-9-5

[5]
Murine Cytomegalovirus and Human Cytomegalovirus Differ in Pyroptosis Induction in Different Cell Types During Productive Replication.

Viruses. 2025-8-12

[6]
CDK5RAP3 Deficiency Is Associated with Hepatic Inflammation and Increased Expression of NLRP3 Inflammasome Components.

Biomedicines. 2025-8-21

[7]
Mechanism of RCD and the Role of Different Death Signaling Pathways in Cancer.

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[8]
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Theranostics. 2025-7-25

[9]
The Effect of Polysaccharide Combined with Cisplatin on LLC1 Lung Cancer.

ACS Omega. 2025-8-5

[10]
PANoptosis in cancer: molecular mechanisms and therapeutic potential.

Cancer Gene Ther. 2025-8-21

本文引用的文献

[1]
Asbestos-induced chronic inflammation in malignant pleural mesothelioma and related therapeutic approaches-a narrative review.

Precis Cancer Med. 2021-9

[2]
The Lysosomal Rag-Ragulator Complex Licenses RIPK1 and Caspase-8-mediated Pyroptosis by .

Science. 2021-6-25

[3]
Microenvironment-Responsive Prodrug-Induced Pyroptosis Boosts Cancer Immunotherapy.

Adv Sci (Weinh). 2021-12

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Molecular mechanisms and functions of pyroptosis in inflammation and antitumor immunity.

Mol Cell. 2021-11-18

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An NIR-Fluorophore-Based Theranostic for Selective Initiation of Tumor Pyroptosis-Induced Immunotherapy.

Small. 2021-9

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Control of gasdermin D oligomerization and pyroptosis by the Ragulator-Rag-mTORC1 pathway.

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Engineered Biomimetic Nanoplatform Protects the Myocardium Against Ischemia/Reperfusion Injury by Inhibiting Pyroptosis.

ACS Appl Mater Interfaces. 2021-7-28

[9]
The metabolite α-KG induces GSDMC-dependent pyroptosis through death receptor 6-activated caspase-8.

Cell Res. 2021-9

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Role of pyroptosis in atherosclerosis and its therapeutic implications.

J Cell Physiol. 2021-10

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