Department of Physiology, School of Medical Sciences, University of Auckland, Private Bag 92014, Auckland, 1142, New Zealand.
Eisdell Moore Centre, University of Auckland, Auckland, New Zealand.
Purinergic Signal. 2022 Dec;18(4):435-450. doi: 10.1007/s11302-022-09896-w. Epub 2022 Sep 29.
Since the discovery of ATP as an extracellular signalling molecule in 1972, purinergic signalling, mediated by extracellular purines and pyrimidines has been identified in virtually all mammalian tissues and is implicated in regulating fundamental cellular processes. In recent years, there has been an increasing focus on the pathophysiology and potential therapeutic interventions based on purinergic signalling. A vast range of compounds targeting purine receptors are in clinical development, and many more are in preclinical studies, which highlights the fast growth in this research field. As a tribute to Professor Geoffrey Burnstock's legacy in purinergic signalling, we present here a brief review of compounds targeting purine receptors that are in different stages of clinical trials. The review highlights the 50-year journey from basic research on purinergic receptors to clinical applications of therapies targeting purine receptors.
自 1972 年发现 ATP 作为细胞外信号分子以来,几乎在所有哺乳动物组织中都发现了由细胞外嘌呤和嘧啶介导的嘌呤能信号转导,并涉及调节基本细胞过程。近年来,人们越来越关注基于嘌呤能信号转导的病理生理学和潜在治疗干预措施。大量针对嘌呤受体的化合物正在进行临床开发,还有更多的化合物处于临床前研究阶段,这突显了该研究领域的快速发展。为了向嘌呤能信号转导领域的杰弗里·伯斯通教授致敬,我们在此简要回顾了处于不同临床试验阶段的靶向嘌呤受体的化合物。该综述突出了从嘌呤能受体的基础研究到针对嘌呤受体的治疗方法的临床应用的 50 年历程。