概述嘌呤能信号传导的作用及其在癌症治疗中的作用。

IF 12 1区 医学 Q1 PHARMACOLOGY & PHARMACY
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引用次数: 0

摘要

由于新型免疫检查点抑制剂(ICI)的问世,癌症疗法的创新在过去十五年中得到了极大的加速。另一方面,自七十年代初以来在嘌呤能信号转导方面积累的显著科学知识终于被应用于临床。目前正在进行几项 I/II 期临床试验,研究干扰嘌呤能信号转导的药物作为独立疗法或联合疗法对癌症的影响。这支持了癌症治疗中 "嘌呤能免疫检查点"(PIC)的新概念。在本综述中,我们将讨论 a) 嘌呤能系统的基础药理学和细胞生物学;b) 嘌呤能系统在人类疾病中的病理生理学原理;c) 嘌呤能系统对细胞死亡、细胞增殖和癌症的影响;d) 研究细胞外环境中核苷酸平衡的新型分子工具;e) P1、P2 受体和相关外酶的药理学最新发展;f) 作为新型诊断工具的 P1 和 P2 配体;g) 基于嘌呤能免疫检查点的抗癌疗法的当前问题。本综述将对癌症中嘌呤能信号转导的现状进行评估,并将有助于确定未来的发展方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overview of the role of purinergic signaling and insights into its role in cancer therapy

Innovation of cancer therapy has received a dramatic acceleration over the last fifteen years thanks to the introduction of the novel immune checkpoint inhibitors (ICI). On the other hand, the conspicuous scientific knowledge accumulated in purinergic signaling since the early seventies is finally being transferred to the clinic. Several Phase I/II clinical trials are currently underway to investigate the effect of drugs interfering with purinergic signaling as stand-alone or combination therapy in cancer. This is supporting the novel concept of “purinergic immune checkpoint” (PIC) in cancer therapy.

In the present review we will address a) the basic pharmacology and cell biology of the purinergic system; b) principles of its pathophysiology in human diseases; c) implications for cell death, cell proliferation and cancer; d) novel molecular tools to investigate nucleotide homeostasis in the extracellular environment; e) recent developments in the pharmacology of P1, P2 receptors and related ecto-enzymes; f) P1 and P2 ligands as novel diagnostic tools; g) current issues in PIC-based anti-cancer therapy.

This review will provide an appraisal of the current status of purinergic signaling in cancer and will help identify future avenues of development.

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来源期刊
CiteScore
23.00
自引率
0.70%
发文量
222
审稿时长
90 days
期刊介绍: Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.
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