Interplay between inflammasomes and PD-1/PD-L1 and their implications in cancer immunotherapy.

IF 3.3 3区 医学 Q2 ONCOLOGY Carcinogenesis Pub Date : 2023-12-30 DOI:10.1093/carcin/bgad072
Zhongyu Jiao, Jun Zhang
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引用次数: 0

Abstract

The inflammasomes play crucial roles in inflammation and cancer development, while the PD-1/PD-L1 pathway is critical for immune suppression in the tumor microenvironment (TME). Recent research indicates a reciprocal regulatory relationship between inflammasomes and PD-1/PD-L1 signaling in cancer development and PD-1 blockade treatment. By activating in diverse cells in tumor tissues, inflammasome upregulates PD-L1 level in the TME. Moreover, the regulation of PD-1/PD-L1 activity by inflammasome activation involves natural killer cells, tumor-associated macrophages and myeloid-derived suppressor cells. Conversely, PD-1 blockade can activate the inflammasome, potentially influencing treatment outcomes. The interplay between inflammasomes and PD-1/PD-L1 has profound and intricate effects on cancer development and treatment. In this review, we discuss the crosstalk between inflammasomes and PD-1/PD-L1 in cancers, exploring their implications for tumorigenesis, metastasis and immune checkpoint inhibitor (ICI) resistance. The combined therapeutic strategies targeting both inflammasomes and checkpoint molecules hold promising potential as treatments for cancer.

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炎症小体与PD-1/PD-L1的相互作用及其在癌症免疫治疗中的意义。
炎症小体在炎症和癌症发展中起着至关重要的作用,而PD-1/PD-L1通路对于肿瘤微环境(TME)中的免疫抑制至关重要。最近的研究表明,炎症小体和PD-1/PD-L1信号在癌症发展和PD-1阻断治疗中存在相互调节关系。炎症小体通过激活肿瘤组织中的不同细胞,上调TME中的PD-L1水平。此外,炎症小体激活对PD-1/PD-L1活性的调节涉及自然杀伤(NK)细胞、肿瘤相关巨噬细胞(TAMs)和髓系抑制细胞(MDSCs)。相反,PD-1阻断剂可以激活炎症小体,可能影响治疗结果。炎症小体和PD-1/PD-L1之间的相互作用对癌症的发展和治疗有着深刻而复杂的影响。在这篇综述中,我们讨论了炎症小体和PD-1/PD-L1在癌症中的相互作用,探讨了它们对肿瘤发生、转移和ICI耐药性的影响。针对炎症小体和检查点分子的联合治疗策略作为癌症的治疗具有很好的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Carcinogenesis
Carcinogenesis 医学-肿瘤学
CiteScore
9.20
自引率
2.10%
发文量
95
审稿时长
1 months
期刊介绍: Carcinogenesis: Integrative Cancer Research is a multi-disciplinary journal that brings together all the varied aspects of research that will ultimately lead to the prevention of cancer in man. The journal publishes papers that warrant prompt publication in the areas of Biology, Genetics and Epigenetics (including the processes of promotion, progression, signal transduction, apoptosis, genomic instability, growth factors, cell and molecular biology, mutation, DNA repair, genetics, etc.), Cancer Biomarkers and Molecular Epidemiology (including genetic predisposition to cancer, and epidemiology), Inflammation, Microenvironment and Prevention (including molecular dosimetry, chemoprevention, nutrition and cancer, etc.), and Carcinogenesis (including oncogenes and tumor suppressor genes in carcinogenesis, therapy resistance of solid tumors, cancer mouse models, apoptosis and senescence, novel therapeutic targets and cancer drugs).
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