## Abstract The antiviral activities of antileukemic drugs 1‐β‐D‐arabinofuranosylcytosine (Cytarabine; Ara‐C), 2,2′‐anhydro‐1‐β‐D‐arabinofuranosylcytosine (Ancitabine; Cyclo‐C), and N^4^‐behenoyl‐1‐β‐D‐arabinofuranosylcytosine (Enocitabine; BH‐AC) were evaluated in vitro against human cytomegalovir
Uptake of 1-β-D-arabinofuranosylcytosine and prednisolone by synchronized human lymphoma cells
✍ Scribed by Persohn, Linda K. ;Drewinko, Benjamin ;Loo, Ti Li
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 386 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0098-1532
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✦ Synopsis
Abstract
The cytotoxicity of many antitumor agents exhibits cell‐cycle phase specificity. Using a human lymphoma cell line synchronized by thymidine block, we have investigated the differential uptake of radioactive 1‐β‐D‐arabinofuranosylcytosine (ara‐C) and prednisolone in various phases of the cycle. Uptake of ara‐C is highest during early S and declines steadily throughout the rest of the cycle. In comparison, prednisolone demonstrates no significant age‐dependent difference in uptake although its cytotoxicity is cell cycle sensitive.
📜 SIMILAR VOLUMES
The effects of N4-behenoyl-l-~-~-arabinofuranosylcytosine (BH-AC) on the cell cycle of murine leukemic cells (L 1210 cells) were compared with those of 1-8-D-arabinofuranosylcytosine (ara-C), known to be effective for acute leukemia. In a cytokinetic study, a combination of Feulgen microcytofluorome
## Abstract 1‐β‐D‐Arabinofuranosylcytosine (ara‐C) was encapsulated in four different types of unsonicated artificial vesicles of phospholipid (liposomes) to compare the anti‐tumor effect on mouse leukemia L1210 inoculated in CD2F, mice with that of free ara‐C. The anti‐tumor activity of ara‐C was