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焦亡性细胞死亡途径在癌症中的多方面作用

The Multifaceted Roles of Pyroptotic Cell Death Pathways in Cancer.

作者信息

Wang Man, Jiang Shuai, Zhang Yinfeng, Li Peifeng, Wang Kun

机构信息

Institute for Translational Medicine, Medical College of Qingdao University, Dengzhou Road 38, 266021 Qingdao, China.

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, 266071 Qingdao, China.

出版信息

Cancers (Basel). 2019 Sep 5;11(9):1313. doi: 10.3390/cancers11091313.

DOI:10.3390/cancers11091313
PMID:31492049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6770479/
Abstract

Cancer is a category of diseases involving abnormal cell growth with the potential to invade other parts of the body. Chemotherapy is the most widely used first-line treatment for multiple forms of cancer. Chemotherapeutic agents act via targeting the cellular apoptotic pathway. However, cancer cells usually acquire chemoresistance, leading to poor outcomes in cancer patients. For that reason, it is imperative to discover other cell death pathways for improved cancer intervention. Pyroptosis is a new form of programmed cell death that commonly occurs upon pathogen invasion. Pyroptosis is marked by cell swelling and plasma membrane rupture, which results in the release of cytosolic contents into the extracellular space. Currently, pyroptosis is proposed to be an alternative mode of cell death in cancer treatment. Accumulating evidence shows that the key components of pyroptotic cell death pathways, including inflammasomes, gasdermins and pro-inflammatory cytokines, are involved in the initiation and progression of cancer. Interfering with pyroptotic cell death pathways may represent a promising therapeutic option for cancer management. In this review, we describe the current knowledge regarding the biological significance of pyroptotic cell death pathways in cancer pathogenesis and also discuss their potential therapeutic utility.

摘要

癌症是一类涉及异常细胞生长并有可能侵袭身体其他部位的疾病。化疗是多种癌症最广泛使用的一线治疗方法。化疗药物通过靶向细胞凋亡途径发挥作用。然而,癌细胞通常会产生化疗耐药性,导致癌症患者预后不佳。因此,发现其他细胞死亡途径以改善癌症干预至关重要。细胞焦亡是一种新的程序性细胞死亡形式,通常在病原体入侵时发生。细胞焦亡的特征是细胞肿胀和质膜破裂,导致胞质内容物释放到细胞外空间。目前,细胞焦亡被认为是癌症治疗中一种替代性的细胞死亡模式。越来越多的证据表明,细胞焦亡性细胞死亡途径的关键成分,包括炎性小体、gasdermin和促炎细胞因子,参与了癌症的发生和发展。干扰细胞焦亡性细胞死亡途径可能是癌症治疗的一个有前景的治疗选择。在这篇综述中,我们描述了关于细胞焦亡性细胞死亡途径在癌症发病机制中的生物学意义的当前知识,并讨论了它们潜在的治疗效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/43c2d35dce66/cancers-11-01313-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/1668c6dfb568/cancers-11-01313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/ddfc54a76f66/cancers-11-01313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/43c2d35dce66/cancers-11-01313-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/1668c6dfb568/cancers-11-01313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/ddfc54a76f66/cancers-11-01313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff0/6770479/43c2d35dce66/cancers-11-01313-g003.jpg

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本文引用的文献

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Evaluation of Canonical Inflammasome Activation in Human Monocytes by Imaging Flow Cytometry.用影像流式细胞仪评估人单核细胞中经典炎症小体的激活。
Front Immunol. 2019 Jun 4;10:1284. doi: 10.3389/fimmu.2019.01284. eCollection 2019.
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Downregulation of hsa_circ_0068087 ameliorates TLR4/NF-κB/NLRP3 inflammasome-mediated inflammation and endothelial cell dysfunction in high glucose conditioned by sponging miR-197.hsa_circ_0068087 的下调通过海绵吸附 miR-197 减轻高糖诱导的 TLR4/NF-κB/NLRP3 炎性小体介导的炎症和内皮细胞功能障碍。
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血小板伪装纳米载体通过触发细胞焦亡改善膀胱癌免疫治疗。
Theranostics. 2024 Oct 14;14(17):6692-6707. doi: 10.7150/thno.99040. eCollection 2024.
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Applications of pyroptosis activators in tumor immunotherapy.焦亡激活剂在肿瘤免疫治疗中的应用。
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Prognostic and chemotherapeutic implications of a novel four-gene pyroptosis model in head and neck squamous cell carcinoma.新型四基因 pyroptosis 模型对头颈部鳞状细胞癌的预后和化疗意义。
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Effect of Radiotherapy on Activating the Pyroptotic Cell Death Pathway in Breast Cancer Patients: The Role of Serum GSDMD-CT, NLRP3 and IL-18.放疗对乳腺癌患者激活细胞焦亡死亡途径的影响:血清 GSDMD-CT、NLRP3 和 IL-18 的作用。
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Ferroptosis: a potential target for the treatment of atherosclerosis.铁死亡:动脉粥样硬化治疗的潜在靶点。
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Extrinsic and intrinsic apoptosis activate pannexin-1 to drive NLRP3 inflammasome assembly.外在和内在凋亡途径激活连接蛋白-1 以驱动 NLRP3 炎性小体组装。
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