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Division of Biochemical Virology, Baylor University College of Medicine, Houston, Texas
1-ß-D-Arabinofuranosylcytosine (ara-C) inhibited growth of monkey kidney, LM, LM(TK-), and HeLa cells and inhibited DNA biosynthesis in monkey kidney and LM cell cultures.
The thymidine (TdR) kinase activities of green monkey kidney (GMK or CV-1) and HeLa, but not LM or LM(TK-), cell cultures were greatly increased after ara-C treatment. A smaller increase of deoxycytidylic (dCMP) deaminase, but not of the thymidylic (TMP) kinase activity, was also found. The induction of TdR kinase activity by ara-C was prevented by cycloheximide.
Addition to the cultures of arabinofuranosylthymine (ara-T), arabinofuranosyluracil (ara-U), TdR, deoxyuridine (UdR), or cytidine did not produce increases in the TdR kinase activity comparable to those produced by ara-C treatment, and the addition of TdR, UdR, or cytidine to cultures treated with ara-C did not alter the ara-C-induced stimulation of TdR kinase.
Ara-T, ara-U, and ara-C did not inhibit either the enzymatic phosphorylation of UdR-3H or the deamination of dCMP-3H. Deoxycytidine, when added to cultures at the same time as ara-C, prevented the increase in TdR kinase and, when added 24 hr after the ara-C treatment, reversed the ara-C induction of TdR kinase.
Mitomycin C (1525 µg/ml), another inhibitor of DNA biosynthesis, induced about a 4-fold increase in the TdR kinase activity. However, TdR kinase activity was not stimulated in cultures treated with 50 or 100 µg/ml mitomycin C.
1 This investigation was aided by grants from the National Science Foundation (GB 3126), the American Cancer Society (E 291), and by USPHS Grants CA-06656, 1-K6-AI-2352, and 1-K3-CA-25, 797.
2 Postdoctoral Fellow of the Consejo Nacional de Investigaciones Científicas y Téenicas (Argentina).
Received 2/ 9/66.
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