白血病中的P2X7受体:病理机制和治疗潜力

IF 2.4 4区 医学 Q2 NEUROSCIENCES
Yanwen Xue, Xiaoxiang Peng, Meng Yan, Yanan Du, Yahui Cao, Ronglan Zhao
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引用次数: 0

摘要

P2X7受体是一个三聚体离子通道嘌呤能受体。它在癌症和多种炎症性疾病的病理生理中起着至关重要的作用,并在不同的细胞类型中广泛表达。白血病是一种影响造血干细胞的恶性克隆性疾病。化疗是白血病的主要治疗方法之一,但也有很多副作用。靶向治疗是近年来出现的一种新的治疗方法。研究表明,白血病的进展和发生与P2X7受体有显著关系。P2X7受体也参与白血病细胞的迁移和侵袭。此外,P2X7受体基因多态性在白血病患者的发生、发展和临床病程中也起着重要的作用。P2X7受体抑制剂已被发现与现有疗法联合使用效果更好。因此,P2X7受体可能作为一个潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The P2X7 receptor in leukemia: pathological mechanisms and therapeutic potential.

The P2X7 receptor is a trimeric ion channel purinergic receptor. It plays a crucial part in the pathophysiology of cancers and a variety of inflammatory diseases and is widely expressed in different cell types. Leukemia represents a type of malignant clonal disorder that impacts the hematopoietic stem cells. Chemotherapy is one of the main treatment methods for leukemia, but there are also many side effects. In recent years, targeted therapy is a new treatment method. Research has shown that the progression and occurrence of leukemia is significantly related to the P2X7 receptor. The P2X7 receptor is also involved in the migration and invasion of leukemia cells. Furthermore, the polymorphism of the P2X7 receptor gene also takes on a significant function in the occurrence, development and clinical course of leukemia patients. The P2X7 receptor inhibitors have been found to work better in combination with existing therapeutics. Therefore, the P2X7 receptor may serve as a potential therapeutic target.

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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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