[Effect of 1-beta-D-arabinofuranosylcytosine on DNA synthesis. 1. In normal rabbit kidney cell cultures].
Albert S. Kaplan, McKay Brown, Tamar Ben‐Porat
Abstract
Albert S. Kaplan, McKay Brown, Tamar Ben‐Porat
Abstract
Low concentrations of 1-β-D-arabinofuranosylcytosine (Ara-C) inhibit the incorporation of cytidine aimd thymidine but stimulate the incorporation of deoxycytidine into the DNA of rabbit kidney cells. This stimulation is correlated with an increase in the level of activity of deoxycytidine kinase and with a consequent increase in the intracellular pool of phosphorylated deoxycytidine derived from the nucleoside in the medium. Ara-C does not prevent the reduction of cytidine diphosphate to deoxycytidine diphosphate in rabbit kidney cells incubated in medium free of deoxycytidine. However, when small amounts of deoxycytidine are supplied to these cells, the drug is effective in inhibiting this reduction, probably as a result of an increase in the intracellular pool of deoxycytidine triphosphate and an ensuing negative feedback inhibition. In agreement with observations made with other systems, in rabbit kidney cells the inhibition of DNA synthesis by the drug can be overcome by deoxycytidine. This reversal is due primarily to a successful competition of deoxycytidine with Ara-C at the level of phosphorylation, thereby preventing the accumulation of the effective inhibitor of DNA synthesis.
OpenAlex reports 16 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Low concentrations of 1-β-D-arabinofuranosylcytosine (Ara-C) inhibit the incorporation of cytidine aimd thymidine but stimulate the incorporation of deoxycytidine into the DNA of rabbit kidney cells. This stimulation is correlated with an increase in the level of activity of deoxycytidine kinase and with a consequent increase in the intracellular pool of phosphorylated deoxycytidine derived from the nucleoside in the medium. Ara-C does not prevent the reduction of cytidine diphosphate to deoxycytidine diphosphate in rabbit kidney cells incubated in medium free of deoxycytidine. However, when small amounts of deoxycytidine are supplied to these cells, the drug is effective in inhibiting this reduction, probably as a result of an increase in the intracellular pool of deoxycytidine triphosphate and an ensuing negative feedback inhibition. In agreement with observations made with other systems, in rabbit kidney cells the inhibition of DNA synthesis by the drug can be overcome by deoxycytidine. This reversal is due primarily to a successful competition of deoxycytidine with Ara-C at the level of phosphorylation, thereby preventing the accumulation of the effective inhibitor of DNA synthesis.
Key concepts: Deoxycytidine, Cytidine, Deoxycytidine kinase, Thymidine, DNA synthesis, Biochemistry, Intracellular, DNA