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针对腺苷 A 受体拮抗作用治疗癌症。

Targeting adenosine A receptor antagonism for treatment of cancer.

机构信息

a Heptares Therapeutics Limited, Steinmetz Building , Cambridge , Granta Park , UK.

b Bioscience, Oncology , IMED Biotech Unit, AstraZeneca , Boston , MA , USA.

出版信息

Expert Opin Drug Discov. 2018 Nov;13(11):997-1003. doi: 10.1080/17460441.2018.1534825. Epub 2018 Oct 18.

Abstract

Adenosine A Receptor (AR) antagonists are an emerging class of agents that treat cancers, both as a monotherapy and in combination with other therapeutic agents. Several studies support the accumulation of extracellular adenosine in the tumor microenvironment as a critical mechanism in immune evasion implicating AR antagonists for use in immuno-oncology. Areas covered: In this perspective article, the authors briefly outline the history of the AR antagonist field for central nervous system indications and give their perspective on the status of agents progressing today in oncology. A brief description of the biological rationale in oncology is given. A particular focus of this article is progress in AR structure determination and its impact on Structure-Based Drug Design. Expert opinion: Our understanding of the AR antagonist mechanism of action has changed and is now being clinically validated by several key companies in the oncology field. This area is likely to rapidly develop over the next 1-2 years.

摘要

腺苷 A 受体 (AR) 拮抗剂是一类新兴的药物,可用于治疗癌症,无论是作为单一疗法还是与其他治疗药物联合使用。多项研究支持肿瘤微环境中细胞外腺苷的积累是免疫逃逸的关键机制,这暗示 AR 拮抗剂可用于免疫肿瘤学。

涵盖领域

在这篇观点文章中,作者简要概述了 AR 拮抗剂在中枢神经系统适应症方面的历史,并对目前在肿瘤学中进展的药物状况提出了自己的看法。文中还简要描述了肿瘤学中的生物学基本原理。本文的一个特别关注点是 AR 结构确定方面的进展及其对基于结构的药物设计的影响。

专家意见

我们对 AR 拮抗剂作用机制的理解已经发生了变化,并且现在正在被肿瘤学领域的几家主要公司通过临床验证。在未来 1-2 年内,该领域可能会迅速发展。

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