P2X7 受体在乳腺癌进展中的作用。

IF 3 4区 医学 Q2 NEUROSCIENCES Purinergic Signalling Pub Date : 2024-07-23 DOI:10.1007/s11302-024-10039-6
Yanan Du, Yahui Cao, Wei Song, Xin Wang, Qingqing Yu, Xiaoxiang Peng, Ronglan Zhao
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引用次数: 0

摘要

乳腺癌是一种常见的恶性肿瘤,发病率逐年上升,已成为女性发病率最高的恶性肿瘤。嘌呤配体门控离子通道7受体(P2X7R)是一种以三磷酸腺苷(ATP)为配体的阳离子通道受体,广泛分布于细胞和组织中,与肿瘤的发生和发展密切相关。P2X7R 通过与 ATP 相互作用,在癌症中发挥着重要作用。研究表明,P2X7R 在乳腺癌中上调,可通过激活蛋白激酶 B(AKT)信号通路、促进上皮-间质转化(EMT)、控制细胞外囊泡(EV)的生成以及调节炎症蛋白环氧化酶 2(COX-2)的表达,促进肿瘤的侵袭和转移。此外,P2X7R 被证明在乳腺癌细胞的增殖和凋亡过程中发挥着重要作用。最近,针对 P2X7R 的抑制剂被发现可以抑制乳腺癌的发展。天然的 P2X7R 拮抗剂,如荷叶碱和异喹啉生物碱小檗碱,也被证明能有效抑制乳腺癌的进展。本文回顾了 P2X7R 与乳腺癌的研究进展,旨在为乳腺癌治疗提供新的靶点和方向。
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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Role of the P2X7 receptor in breast cancer progression.

Breast cancer is a common malignant tumor, whose incidence is increasing year by year, and it has become the malignant tumor with the highest incidence rate in women. Purine ligand-gated ion channel 7 receptor (P2X7R) is a cation channel receptor with Adenosine triphosphate ( ATP) as a ligand, which is widely distributed in cells and tissues, and is closely related to tumorigenesis and progression. P2X7R plays an important role in cancer by interacting with ATP. Studies have shown that P2X7R is up-regulated in breast cancer and can promote tumor invasion and metastasis by activating the protein kinase B (AKT) signaling pathway, promoting epithelial-mesenchymal transition (EMT), controlling the generation of extracellular vesicle (EV), and regulating the expression of the inflammatory protein cyclooxygenase 2 (COX-2). Furthermore, P2X7R was proven to play an essential role in the proliferation and apoptosis of breast cancer cells. Recently, inhibitors targeting P2X7R have been found to inhibit the progression of breast cancer. Natural P2X7R antagonists, such as rhodopsin, and the isoquinoline alkaloid berberine, have also been shown to be effective in inhibiting breast cancer progression. In this article, we review the research progress of P2X7R and breast cancer intending to provide new targets and directions for breast cancer treatment.

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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.
期刊最新文献
Correction to: Preparation and preliminary evaluation of a tritium-labeled allosteric P2X4 receptor antagonist. Machine learning-aided search for ligands of P2Y6 and other P2Y receptors. Purinergic regulation of pulmonary vascular tone. Role of ecto-5'-nucleotidase in bladder function activity and smooth muscle contractility. Unexpected role of microglia and P2Y12 in the induction of and emergence from anesthesia.
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