Treatment of normal and malignant cells with nucleoside analogues and etoposide enhances deoxycytidine kinase activity

Author:

Spasokoukotskaja T.,Sasvári-Székely M.,Keszler G.,Albertioni F.,Eriksson S.,Staub M.

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference29 articles.

1. Mammalian deoxyribonucleoside kinases;Arnér;Pharmacol. Ther.,1995

2. Comparison of the substrate specificities of human thymidine kinase 1 and 2 and deoxycytidine kinase toward antiviral and cytostatic nucleoside analogs;Eriksson;Biochem. Biophys. Res. Commun.,1991

3. Effects of 2-chloro-9-(2-deoxy-2-fluoro-β-d-arabinofuranosyl)adenine on K562 cellular metabolism and the inhibition of human ribonucleotide reductase and DNA polymerases by its 5′-triphosphate;Parker;Cancer Res.,1991

4. Deoxynucleotide pool depletion and sustained inhibition of ribonucleotide reductase and DNA synthesis after treatment of human lymphoblastoid cells with 2-chloro-9-(2-deoxy-2-fluoro-β-d-arabinofuranosyl)adenine;Xie;Cancer Res.,1996

5. Characterisation of deoxycytidine kinase promoter in human lymphoblastoid cell lines;Chen;J. Clin. Invest.,1995

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