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NLRP3 炎性小体激活在辐射损伤中的作用。

The role of NLRP3 inflammasome activation in radiation damage.

机构信息

Department of Radiation Oncology, The First Hospital, Jilin University, Changchun, 130021, China.

Department of Internal Medicine, Florida Hospital, Orlando, FL, 32803, USA.

出版信息

Biomed Pharmacother. 2019 Oct;118:109217. doi: 10.1016/j.biopha.2019.109217. Epub 2019 Jul 11.


DOI:10.1016/j.biopha.2019.109217
PMID:31302424
Abstract

Radiotherapy (RT) is currently one of the leading treatment for various cancers and it may cause injury to healthy tissue, with both short-term and long-term side effects. Inflammatory responses play an important role in the adverse reactions of early and late ionizing radiation. Nucleotide-binding domain and leucine-rich-repeat-containing family pyrin 3 (NLRP3) inflammasome as a multi-protein complex that activates caspase-1 can give rise to the proinflammatory cytokines such as interleukin-18 (IL-18) and interleukin-1 beta (IL-1β) maturation. Recent experiments and studies have shown that up-regulation of NLRP3 inflammasome have a big impact on radiation damage, which include radiation-induced oral mucositis, radiation-induced skin reactions, radiation-induced lung damage, radiation-induced intestinal injury and radiation-induced changes in other systems. In this paper, we will review the role of NLRP3 inflammasome in radiation damage, to explore possible therapeutic strategies for radiation damage.

摘要

放射治疗(RT)目前是治疗各种癌症的主要方法之一,它可能会对健康组织造成损伤,产生短期和长期的副作用。炎症反应在电离辐射的不良反应中起着重要作用。核苷酸结合域和富含亮氨酸重复序列的含pyrin 3(NLRP3)炎性小体作为一种能够激活半胱天冬酶-1的多蛋白复合物,可以导致白细胞介素-18(IL-18)和白细胞介素-1β(IL-1β)等促炎细胞因子的成熟。最近的实验和研究表明,NLRP3 炎性小体的上调对辐射损伤有很大的影响,包括辐射诱导的口腔粘膜炎、辐射诱导的皮肤反应、辐射诱导的肺损伤、辐射诱导的肠道损伤以及辐射诱导的其他系统的改变。本文将综述 NLRP3 炎性小体在辐射损伤中的作用,探讨辐射损伤的可能治疗策略。

相似文献

[1]
The role of NLRP3 inflammasome activation in radiation damage.

Biomed Pharmacother. 2019-7-11

[2]
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Mol Neurobiol. 2016-7

[3]
Regulation and Function of the Nucleotide Binding Domain Leucine-Rich Repeat-Containing Receptor, Pyrin Domain-Containing-3 Inflammasome in Lung Disease.

Am J Respir Cell Mol Biol. 2016-2

[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Targeted prevention of radiation-induced oral mucositis by glutathione-modified liposome coated K12 probiotics and clinical study.

Mater Today Bio. 2025-7-29

[2]
Molecular docking analysis of inhibitory effect of phytochemicals present in Yogaraja Guggulu on inflammation - implication in adjunctive management of radiation mucositis of oral cavity: An experimental study.

Medicine (Baltimore). 2025-7-18

[3]
Regulation of cancer by inflammasomes: from inflammation to tumorigenesis.

Front Immunol. 2025-7-7

[4]
ROS-regulated SUR1-TRPM4 drives persistent activation of NLRP3 inflammasome in microglia after whole-brain radiation.

Acta Neuropathol Commun. 2025-1-27

[5]
Ferulic Acid Interferes with Radioactive Intestinal Injury Through the DJ-1-Nrf2 and Sirt1-NF-κB-NLRP3 Pathways.

Molecules. 2024-10-26

[6]
[Effects of Ionizing Radiation on Intestinal Bile Acid Metabolism: Mechanism of the Radioprotective Effect of Glycoursodeoxycholic Acid].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2024-9-20

[7]
Radiation-induced skin reactions: oxidative damage mechanism and antioxidant protection.

Front Cell Dev Biol. 2024-10-9

[8]
Suppression of NLRP3 inflammasome activation by astragaloside IV via promotion of mitophagy to ameliorate radiation-induced renal injury in mice.

Transl Androl Urol. 2024-1-31

[9]
Glycyrrhizin alleviates radiation-induced lung injury by regulating the NLRP3 inflammasome through endoplasmic reticulum stress.

Toxicol Res (Camb). 2024-1-25

[10]
Age-related exacerbation of lung damage after trauma is associated with increased expression of inflammasome components.

Front Immunol. 2024-1-11

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