POTENTIATION OF 2',3'-DIDEOXYCYTIDINE (DDC) BY HYDROXYUREA AND THYMIDINE ON THE MOLONEY MURINE LEUKEMIA-VIRUS (MOMLV) EARLY REPLICATIVE STEPS

Citation
H. Goulaouic et al., POTENTIATION OF 2',3'-DIDEOXYCYTIDINE (DDC) BY HYDROXYUREA AND THYMIDINE ON THE MOLONEY MURINE LEUKEMIA-VIRUS (MOMLV) EARLY REPLICATIVE STEPS, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(5), 1994, pp. 430-436
Citations number
24
Categorie Soggetti
Multidisciplinary Sciences
ISSN journal
07644469
Volume
317
Issue
5
Year of publication
1994
Pages
430 - 436
Database
ISI
SICI code
0764-4469(1994)317:5<430:PO2(BH>2.0.ZU;2-G
Abstract
Combinations of ddC with either the ribonucleotide reductase inhibitor hydroxyurea (HU) or with the natural nucleoside thymidine have been i nvestigated on the cycle of a defective (psi neo) Moloney Leukemia Vir us (MoMLV) using 3T3 fibroblasts as host cells. In this experimental m odel, ddC displayed very poor antiviral action which was obvious given an IC50 value close to 100 muM, i.e. an efficiency about thirty thous and fold lower than that of AZT. Both HU and thymidine alone resulted in significant inhibition of MoMLV replication with IC50 values of 40 muM and 100 muM respectively. The combination of ddC with 50 muM HU lo wered the IC50 of ddC by a factor of 10. A similar but more pronounced effect was obtained by combining ddC and 100 muM thymidine, which dec reases the IC50 value of ddC by a factor of 50. Combining 40 muM ddC a nd 100 muM thymidine resulted in the quite complete inhibition of vira l replication. These results show that in cell types with strongly res tricted ddC action, combination treatment with compounds known to ulti mately decrease dCTP biosynthesis leads to the restoration of efficien t antiviral activity.