Nucleotide signaling in neutrophils: a key player in cancer dynamics.

IF 2.5 4区 医学 Q2 NEUROSCIENCES
Jean Lucas Gutknecht da Silva, Jean Sévigny, Daniela Bitencourt Rosa Leal
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引用次数: 0

Abstract

Neutrophils are key innate immune cells whose effector mechanisms are increasingly recognized as therapeutic targets in chronic inflammation and cancer. While highly heterogeneous and functionally versatile, they can also exacerbate inflammation and tissue damage, making precise modulation critical for homeostasis. Nucleotide signaling-including extracellular nucleotide-metabolizing enzymes and receptors for ATP, UTP, and adenosine-plays a central role in regulating neutrophil responses. Extracellular nucleotides influence adhesion, chemotaxis, and degranulation, with important implications in cancer. Neutrophil heterogeneity affects tumor progression through both pro- and antitumor mechanisms. This review summarizes these findings and highlights therapeutic strategies targeting nucleotide signaling to modulate neutrophil activity in cancer.

中性粒细胞中的核苷酸信号:癌症动力学中的关键角色。
中性粒细胞是关键的先天免疫细胞,其效应机制越来越被认为是慢性炎症和癌症的治疗靶点。虽然高度异质性和功能多样,但它们也会加剧炎症和组织损伤,因此精确调节对体内平衡至关重要。核苷酸信号——包括胞外核苷酸代谢酶和ATP、UTP和腺苷受体——在调节中性粒细胞反应中起着核心作用。细胞外核苷酸影响粘附、趋化性和脱颗粒,在癌症中具有重要意义。中性粒细胞异质性通过促肿瘤和抗肿瘤机制影响肿瘤进展。本文综述了这些发现,并重点介绍了针对核苷酸信号调节肿瘤中性粒细胞活性的治疗策略。
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
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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