Comprehensive insights into potential roles of purinergic P2 receptors on diseases: Signaling pathways involved and potential therapeutics

IF 11.4 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Yanshuo Guo , Tianqi Mao , Yafei Fang , Hui Wang , Jiayue Yu , Yifan Zhu , Shige Shen , Mengze Zhou , Huanqiu Li , Qinghua Hu
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引用次数: 0

Abstract

Background

Purinergic P2 receptors, which can be divided into ionotropic P2X receptors and metabotropic P2Y receptors, mediate cellular signal transduction of purine or pyrimidine nucleoside triphosphates and diphosphate. Based on the wide expression of purinergic P2 receptors in tissues and organs, their significance in homeostatic maintenance, metabolism, nociceptive transmission, and other physiological processes is becoming increasingly evident, suggesting that targeting purinergic P2 receptors to regulate biological functions and signal transmission holds significant promise for disease treatment.

Aim of review

This review highlights the detailed mechanisms by which purinergic P2 receptors engage in physiological and pathological progress, as well as providing prospective strategies for discovering clinical drug candidates.

Key scientific concepts of review

The purinergic P2 receptors regulate complex signaling and molecular mechanisms in nervous system, digestive system, immune system and as a result, controlling physical health states and disease progression. There has been a significant rise in research and development focused on purinergic P2 receptors, contributing to an increased number of drug candidates in clinical trials. A few influential pioneers have laid the foundation for advancements in the evaluation, development, and of novel purinergic P2 receptors modulators, including agonists, antagonists, pharmaceutical compositions and combination strategies, despite the different scaffolds of these drug candidates. These advancements hold great potential for improving therapeutic outcomes by specifically targeting purinergic P2 receptors.

Abstract Image

Abstract Image

全面了解嘌呤能 P2 受体对疾病的潜在作用:相关信号通路和潜在疗法
嘌呤能 P2 受体可分为离子型 P2X 受体和代谢型 P2Y 受体,介导嘌呤或嘧啶核苷三磷酸酯和二磷酸的细胞信号传导。基于嘌呤能 P2 受体在组织和器官中的广泛表达,它们在平衡维持、新陈代谢、痛觉传导和其他生理过程中的重要性日益明显,这表明以嘌呤能 P2 受体为靶点调节生物功能和信号传导在疾病治疗中大有可为。本综述重点介绍了嘌呤能 P2 受体参与生理和病理过程的详细机制,并提供了发现临床候选药物的前瞻性策略。嘌呤能 P2 受体调节神经系统、消化系统和免疫系统中复杂的信号传递和分子机制,从而控制身体健康状态和疾病进展。以嘌呤能 P2 受体为重点的研究和开发大幅增加,促使越来越多的候选药物进入临床试验阶段。尽管这些候选药物的支架各不相同,但一些有影响力的先驱已为新型嘌呤能 P2 受体调节剂(包括激动剂、拮抗剂、药物组合和组合策略)的评估、开发和应用奠定了基础。这些进展为通过特异性靶向嘌呤能 P2 受体改善治疗效果带来了巨大潜力。
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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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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