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Abstract
Currently, the most promising therapeutic modality for cancer treatment is the blockade
of immune checkpoint pathways, which has revolutionized cancer therapy in the past
15 years. Strategies targeting and modulating adenosine A2A receptor (A2AR), an emerging
alternative immune checkpoint, have shown the potential to produce significant therapeutic
effects. In this review, we describe the immunosuppressive activities of A2AR and
A2BR in the tumor microenvironment (TME), followed by a summary and discussion of
the structure-activity relationship (SAR) of the A2AR (and dual A2AR/A2BR) antagonists
that have been experimentally confirmed to exert oncoimmunological effects. This review
also provides an update on the compounds under clinical evaluation and insights into
the ligand binding modes of the receptor.