Putative role of the adenosine A3 receptor in the antiproliferative action of N 6-(2-isopentenyl)adenosine
Autor: | Henk de Vries, Sara Bar-Yehuda, Thea Mulder-Krieger, Jacobien K. Von Frijtag Drabbe Künzel, Pnina Fishman, Clara C. Blad, Adriaan P. IJzerman |
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Rok vydání: | 2011 |
Předmět: |
Agonist
medicine.drug_class Modified nucleoside Biology Cellular and Molecular Neuroscience LNCaP medicine Adenosine A3 receptor skin and connective tissue diseases Receptor Molecular Biology Chinese hamster ovary cell Antitumor agent Cell Biology Zeatin riboside bacterial infections and mycoses Adenosine Adenosine receptor respiratory tract diseases N6-(2-isopentenyl)adenosine (IPA) Biochemistry Original Article HPLC Nucleoside medicine.drug |
Zdroj: | Purinergic Signalling |
ISSN: | 1573-9546 1573-9538 |
Popis: | We tested a panel of naturally occurring nucleosides for their affinity towards adenosine receptors. Both N6-(2-isopentenyl)adenosine (IPA) and racemic zeatin riboside were shown to be selective human adenosine A3 receptor (hA3R) ligands with affinities in the high nanomolar range (Ki values of 159 and 649 nM, respectively). These values were comparable to the observed Ki value of adenosine on hA3R, which was 847 nM in the same radioligand binding assay. IPA also bound with micromolar affinity to the rat A3R. In a functional assay in Chinese hamster ovary cells transfected with hA3R, IPA and zeatin riboside inhibited forskolin-induced cAMP formation at micromolar potencies. The effect of IPA could be blocked by the A3R antagonist VUF5574. Both IPA and reference A3R agonist 2-chloro-N6-(3-iodobenzyl)adenosine-5′-N-methylcarboxamide (Cl-IB-MECA) have known antitumor effects. We demonstrated strong and highly similar antiproliferative effects of IPA and Cl-IB-MECA on human and rat tumor cell lines LNCaP and N1S1. Importantly, the antiproliferative effect of low concentrations of IPA on LNCaP cells could be fully blocked by the selective A3R antagonist MRS1523. At higher concentrations, IPA appeared to inhibit cell growth by an A3R-independent mechanism, as was previously reported for other A3R agonists. We used HPLC to investigate the presence of endogenous IPA in rat muscle tissue, but we could not detect the compound. In conclusion, the antiproliferative effects of the naturally occurring nucleoside IPA are at least in part mediated by the A3R. Electronic supplementary material The online version of this article (doi:10.1007/s11302-011-9244-9) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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