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