Hunting down NLRP3 inflammasome: An executioner of radiation-induced injury

被引:15
作者
Cheng, Han [1 ,2 ]
Chen, Lingling [1 ,2 ]
Huang, Minchun [2 ]
Hou, Jin [2 ]
Chen, Zhifeng [2 ]
Yang, Xiaojun [2 ]
机构
[1] Southern Med Univ, Sch Clin Med 1, Guangzhou, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Stomatol, Guangzhou, Peoples R China
关键词
NLRP3; inflammasome; inflammasome activation; radiation injury; therapeutic target; ROS; pyroptosis; NORMAL TISSUE; OXIDATIVE STRESS; DNA-DAMAGE; CELL-DEATH; KAPPA-B; ACTIVATION; FIBROSIS; RADIOTHERAPY; MECHANISMS; PYROPTOSIS;
D O I
10.3389/fimmu.2022.967989
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Radiotherapy is one of the mainstream treatment modalities for several malignancies. However, radiation-induced injury to surrounding normal tissues limits its efficacy. The NLRP3 inflammasome is an essential mechanism of innate immunity that reacts to challenges from endogenous danger signals and pathological microbes. A growing body of evidence has demonstrated a key role of NLRP3 inflammasome in the pathogenesis of radiation-induced tissue injury. Despite accumulating evidence, the potential value of the NLRP3 inflammasome in the management of radiation-induced tissue injury is not adequately recognized. We conducted a literature review to characterize the relationship between NLRP3 inflammasome and radiation injury. By analyzing recent evidence, we identify NLRP3 inflammasome as one of the executioners of radiation-induced injury, since it responds to the challenges of radiation, induces cell pyroptosis and tissue dysfunction, and initiates non-resolving inflammation and fibrosis. Based on these concepts, we propose early intervention/prevention strategies targeting NLRP3 inflammasome in a radiation context, which may help resolve imperative clinical problems.
引用
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页数:16
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