Differential role of the NLRP3 inflammasome in infection and tumorigenesis

被引:74
作者
Tartey, Sarang [1 ]
Kanneganti, Thirumala-Devi [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, MS-351,262 Danny Thomas Pl, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
inflammasome; inflammation; tumorigenesis; TOLL-LIKE RECEPTORS; NOD-LIKE RECEPTORS; NF-KAPPA-B; HOST-DEFENSE; CASPASE-1; ACTIVATION; CATHEPSIN-B; NEUTROPHIL RECRUITMENT; INFLUENZA-VIRUS; ADIPOSE-TISSUE; TH17; RESPONSES;
D O I
10.1111/imm.13046
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dysregulated inflammation is one of the hallmarks of cancer initiation and progression. Emerging evidence indicates that inflammasomes play a central role in regulating immune cell functions in various infections and cancer. Inflammasomes are multimeric complexes consisting of nucleotide-binding oligomerization domain (NOD) -like receptors (NLRs). Among the NLRs, NOD1, NOD2 and NLRP3 respond to a variety of endogenous (i.e. damage-associated molecular patterns) and exogenous (i.e. pathogen-associated molecular patterns) stimuli. The NLRP3 inflammasome is associated with the onset and progression of autoinflammatory and autoimmune diseases, including metabolic disorders, multiple sclerosis, inflammatory bowel disease, and cryopyrin-associated periodic fever syndrome. NLRP3 is also associated with a wide variety of infections and tumorigenesis that are closely correlated with chemotherapy response and prognosis. In this review, we explore the rapidly expanding body of research on the expression and functions of NLRP3 in infections and cancers and outline novel inhibitors targeting the NLRP3 inflammasome that could be developed as therapeutic alternatives to current anticancer treatment.
引用
收藏
页码:329 / 338
页数:10
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