Abstract |
We studied the cytotoxicity of acadesine (5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside) for tumor and normal cells of various species and tissue origin. In tumor cells, acadesine triggered non-apoptotic death; the potency of the compound to normal cells was substantially lower. Acadesine was toxic for tumor cells with multidrug resistant phenotypes caused by the transmembrane transporter Р- glycoprotein or lack of proapoptotic p53. Activity of adenosine receptors was required for acadesine-induced cell death, whereas functioning of АМР-dependent protein kinase was not required. A more pronounced cytotoxicity for tumor cells, as well as the non-canonical death mechanism(s), makes acadesine a promising candidate for antitumor therapy.
|
Authors | V A Glazunova, K V Lobanov, R S Shakulov, A S Mironov, A A Shtil |
Journal | Acta naturae
(Acta Naturae)
Vol. 5
Issue 3
Pg. 74-8
(Jul 2013)
ISSN: 2075-8251 [Print] Russia (Federation) |
PMID | 24303202
(Publication Type: Journal Article)
|