Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists

The A<sub>2A</sub> adenosine receptor (A<sub>2A</sub>AR) plays critical roles in human physiology and pathophysiology, which makes it an important drug target. Previous drug-discovery efforts targeting the A<sub>2A</sub>AR have been focused on the use of A<sub&...

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Main Authors: Jinfeng Zhang, Wenzhong Yan, Wenwen Duan, Kurt Wüthrich, Jianjun Cheng
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/13/9/237
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spelling doaj-14504f5166644762b43ed8fa583b9d562020-11-25T03:00:09ZengMDPI AGPharmaceuticals1424-82472020-09-011323723710.3390/ph13090237Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor AntagonistsJinfeng Zhang0Wenzhong Yan1Wenwen Duan2Kurt Wüthrich3Jianjun Cheng4iHuman Institute, ShanghaiTech University, Shanghai 201210, ChinaiHuman Institute, ShanghaiTech University, Shanghai 201210, ChinaiHuman Institute, ShanghaiTech University, Shanghai 201210, ChinaiHuman Institute, ShanghaiTech University, Shanghai 201210, ChinaiHuman Institute, ShanghaiTech University, Shanghai 201210, ChinaThe A<sub>2A</sub> adenosine receptor (A<sub>2A</sub>AR) plays critical roles in human physiology and pathophysiology, which makes it an important drug target. Previous drug-discovery efforts targeting the A<sub>2A</sub>AR have been focused on the use of A<sub>2A</sub>AR antagonists for the treatment of Parkinson’s disease. More recently, the A<sub>2A</sub>AR has attracted additional attention for its roles in immuno-oncology, and a number of A<sub>2A</sub>AR antagonists are currently used as lead compounds for antitumor drugs in both preclinical models and clinical trials. This review surveys recent advances in the development of A<sub>2A</sub>AR antagonists for cancer immunotherapy. The therapeutic potential of representative A<sub>2A</sub>AR antagonists is discussed based on both animal efficacy studies and clinical data.https://www.mdpi.com/1424-8247/13/9/237GPCRimmuno-oncologyParkinson’s diseasedrug binding modescancer therapy
collection DOAJ
language English
format Article
sources DOAJ
author Jinfeng Zhang
Wenzhong Yan
Wenwen Duan
Kurt Wüthrich
Jianjun Cheng
spellingShingle Jinfeng Zhang
Wenzhong Yan
Wenwen Duan
Kurt Wüthrich
Jianjun Cheng
Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
Pharmaceuticals
GPCR
immuno-oncology
Parkinson’s disease
drug binding modes
cancer therapy
author_facet Jinfeng Zhang
Wenzhong Yan
Wenwen Duan
Kurt Wüthrich
Jianjun Cheng
author_sort Jinfeng Zhang
title Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
title_short Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
title_full Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
title_fullStr Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
title_full_unstemmed Tumor Immunotherapy Using A<sub>2A</sub> Adenosine Receptor Antagonists
title_sort tumor immunotherapy using a<sub>2a</sub> adenosine receptor antagonists
publisher MDPI AG
series Pharmaceuticals
issn 1424-8247
publishDate 2020-09-01
description The A<sub>2A</sub> adenosine receptor (A<sub>2A</sub>AR) plays critical roles in human physiology and pathophysiology, which makes it an important drug target. Previous drug-discovery efforts targeting the A<sub>2A</sub>AR have been focused on the use of A<sub>2A</sub>AR antagonists for the treatment of Parkinson’s disease. More recently, the A<sub>2A</sub>AR has attracted additional attention for its roles in immuno-oncology, and a number of A<sub>2A</sub>AR antagonists are currently used as lead compounds for antitumor drugs in both preclinical models and clinical trials. This review surveys recent advances in the development of A<sub>2A</sub>AR antagonists for cancer immunotherapy. The therapeutic potential of representative A<sub>2A</sub>AR antagonists is discussed based on both animal efficacy studies and clinical data.
topic GPCR
immuno-oncology
Parkinson’s disease
drug binding modes
cancer therapy
url https://www.mdpi.com/1424-8247/13/9/237
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