Multifaceted Roles of the NLRC4 Inflammasome in Cancer: From Molecular Mechanisms to Therapeutic Implications.

IF 4.5 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zhen Zhang, Yang Li, Zhimeng Lv, Si Ming Man
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引用次数: 0

Abstract

NLRC4 forms an inflammasome complex and activates a critical innate immune response to bacterial infection. The NLRC4 inflammasome triggers the activation of the cysteine protease caspase-1, leading to the proteolytic maturation of the pro-inflammatory cytokines IL-1β and IL-18, and the induction of pyroptosis. The role of NLRC4 in antimicrobial defense is well-established, but emerging evidence highlights a complex and often paradoxical functions of NLRC4 in the development and progression of cancer. NLRC4 acts as a tumor suppressor in colorectal and intestinal cancer, and potentially melanoma. NLRC4 also forms unique tumor-attenuating protein complexes, independently of NAIPs, ASC and caspase-1, that activate the DNA damage response. In obesity-associated cancers and metastasis, NLRC4 is pro-tumorigenic and promotes pathological inflammation and angiogenesis. Understanding the precise regulatory mechanisms of NLRC4 in cancer will provide insights into the development of personalized immunotherapies. This review discusses the multi-functional roles of NLRC4 in cancer and explores the potential clinical utility of targeting NLRC4 in therapies.

NLRC4炎症小体在癌症中的多面作用:从分子机制到治疗意义
NLRC4形成炎性小体复合物并激活对细菌感染的关键先天免疫反应。NLRC4炎性小体触发半胱氨酸蛋白酶caspase-1的激活,导致促炎细胞因子IL-1β和IL-18的蛋白水解成熟,并诱导焦亡。NLRC4在抗微生物防御中的作用已经确立,但新出现的证据强调了NLRC4在癌症发生和进展中的复杂且往往矛盾的功能。NLRC4在结直肠癌和肠癌以及潜在的黑色素瘤中起肿瘤抑制作用。NLRC4还形成独特的肿瘤衰减蛋白复合物,独立于NAIPs、ASC和caspase-1,激活DNA损伤反应。在肥胖相关的癌症和转移中,NLRC4促进肿瘤发生,促进病理性炎症和血管生成。了解NLRC4在癌症中的精确调控机制将为个性化免疫疗法的发展提供见解。本文讨论了NLRC4在癌症中的多种功能作用,并探讨了靶向NLRC4治疗的潜在临床应用。
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
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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