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三磷酸腺苷门控 P2X7 受体拮抗剂:癌症治疗的潜在策略。

Antagonism of the ATP-gated P2X7 receptor: a potential therapeutic strategy for cancer.

机构信息

Department of Neuroscience, Faculty of Medicine, Nursing and Health Sciences, Central Clinical School, Monash University, Melbourne, VIC, Australia.

Department of Physiology, Melbourne University, Parkville, VIC, Australia.

出版信息

Purinergic Signal. 2021 Jun;17(2):215-227. doi: 10.1007/s11302-021-09776-9. Epub 2021 Mar 17.

Abstract

The P2X receptor 7 (P2X7R) is a plasma membrane receptor sensing extracellular ATP associated with a wide variety of cellular functions. It is most commonly expressed on immune cells and is highly upregulated in a number of human cancers where it can play a trophic role in tumorigenesis. Activation of this receptor leads to the formation of a non-selective cation channel, which has been associated with several cellular functions mediated by the PI3K/Akt pathway and protein kinases. Due to its broad range of functions, the receptor represents a potential therapeutic target for a number of cancers. This review describes the range of mechanisms associated with P2X7R activation in cancer settings and highlights the potential of targeted inhibition of P2X7R as a therapy. It also describes in detail a number of key P2X7R antagonists currently in pre-clinical and clinical development, including oxidised ATP, Brilliant Blue G (BBG), KN-62, KN-04, A740003, A438079, GSK1482160, CE-224535, JNJ-54175446, JNJ-55308942, and AZ10606120. Lastly, it summarises the in vivo studies and clinical trials associated with the use and development of these P2X7R antagonists in different disease contexts.

摘要

P2X 受体 7(P2X7R)是一种质膜受体,可感应与多种细胞功能相关的细胞外 ATP。它最常表达于免疫细胞,在许多人类癌症中高度上调,在这些癌症中,它可以在肿瘤发生中发挥营养作用。该受体的激活导致非选择性阳离子通道的形成,该通道与 PI3K/Akt 途径和蛋白激酶介导的几种细胞功能有关。由于其广泛的功能,该受体代表了多种癌症的潜在治疗靶点。本综述描述了与癌症环境中 P2X7R 激活相关的一系列机制,并强调了靶向抑制 P2X7R 作为一种治疗方法的潜力。它还详细描述了目前处于临床前和临床开发阶段的几种关键 P2X7R 拮抗剂,包括氧化型 ATP、亮蓝 G(BBG)、KN-62、KN-04、A740003、A438079、GSK1482160、CE-224535、JNJ-54175446、JNJ-55308942 和 AZ10606120。最后,它总结了与这些 P2X7R 拮抗剂在不同疾病环境中的使用和开发相关的体内研究和临床试验。

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