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Cancer‐related somatic mutations alter adenosine A 1 receptor pharmacology—A focus on mutations in the loops and C‐terminus
Author(s) -
Wang Xuesong,
Jespers Willem,
Waal Just J.,
Wolff Kim A. N.,
Uden Liedeke,
IJzerman Adriaan P.,
Westen Gerard J. P.,
Heitman Laura H.
Publication year - 2022
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.202200203rr
Subject(s) - g protein coupled receptor , mutant , receptor , agonist , transmembrane domain , biology , mutation , 5 ht5a receptor , adenosine a2b receptor , extracellular , adenosine receptor , microbiology and biotechnology , cancer research , genetics , gene
G protein‐coupled receptors (GPCRs) are known to be involved in tumor progression and metastasis. The adenosine A 1 receptor (A 1 AR) has been detected to be over‐expressed in various cancer cell lines. However, the role of A 1 AR in tumor development is not yet well characterized. A series of A 1 AR mutations were identified in the Cancer Genome Atlas from cancer patient samples. In this study, we have investigated the pharmacology of mutations located outside of the 7‐transmembrane domain by using a “single‐GPCR‐one‐G protein” yeast system. Concentration‐growth curves were obtained with the full agonist CPA for 12 mutant receptors and compared to the wild‐type hA 1 AR. Most mutations located at the extracellular loops (EL) reduced the levels of constitutive activity of the receptor and agonist potency. For mutants at the intracellular loops (ILs) of the receptor, an increased constitutive activity was found for mutant receptor L211R 5.69 , while a decreased constitutive activity and agonist response were found for mutant receptor L113F 34.51 . Lastly, mutations identified on the C‐terminus did not significantly influence the pharmacological function of the receptor. A selection of mutations was also investigated in a mammalian system. Overall, similar effects on receptor activation compared to the yeast system were found with mutations located at the EL, but some contradictory effects were observed for mutations located at the IL. Taken together, this study will enrich the insight of A 1 AR structure and function, enlightening the consequences of these mutations in cancer. Ultimately, this may provide potential precision medicine in cancer treatment.