P2 receptors signaling in the esophagus: from inflammation to cancer.

IF 3 4区 医学 Q2 NEUROSCIENCES
Aline Zaparte, Fernanda F Cruz, Julia B de Souza, Fernanda B Morrone
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引用次数: 0

Abstract

The signaling mechanisms of nucleotides and nucleosides have been extensively studied over the past decades in various conditions affecting distinct organs and tissues. It is well-established that purinergic receptors are expressed in healthy tissues, with expression levels often increasing under pathological conditions. These receptors play crucial roles in numerous physiological and pathological processes, including inflammation, tissue repair, and cellular signaling. However, the purinergic context in the esophagus and its associated pathologies remains poorly understood, representing a significant gap in current knowledge. In this review, we compiled and analyzed the available data on the involvement of P2 purinergic receptors in esophageal diseases, such as gastroesophageal reflux disease and esophageal carcinoma. Specifically, we discuss the pharmacological modulation, functional characterization, and expression patterns of these receptors in various esophageal cell lines and immune tissue samples, under both healthy and pathological conditions. Understanding the mechanisms of action and signaling pathways involving P2 purinergic receptors in the esophagus can offer valuable insights into their biological roles and emphasize their potential as therapeutic targets for future clinical applications.

食道P2受体信号:从炎症到癌症。
在过去的几十年里,在影响不同器官和组织的各种条件下,核苷酸和核苷的信号传导机制已经被广泛研究。嘌呤能受体在健康组织中表达,在病理条件下表达水平往往增加。这些受体在许多生理和病理过程中发挥重要作用,包括炎症、组织修复和细胞信号传导。然而,食道的嘌呤能背景及其相关病理仍然知之甚少,这代表了当前知识的重大差距。本文对P2嘌呤能受体在胃食管反流病和食管癌等食道疾病中的作用进行综述和分析。具体来说,我们讨论了在健康和病理条件下,这些受体在各种食管细胞系和免疫组织样本中的药理调节、功能表征和表达模式。了解P2嘌呤能受体在食道中的作用机制和信号通路可以为其生物学作用提供有价值的见解,并强调其作为未来临床应用的治疗靶点的潜力。
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
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.
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