In vitro cytotoxic effects of fludarabine (2-F-ara-A) in combination with commonly used antileukemic agents by isobologram analysis
Open Access
- 1 March 2000
- journal article
- research article
- Published by Springer Nature in Leukemia
- Vol. 14 (3) , 379-388
- https://doi.org/10.1038/sj.leu.2401684
Abstract
Fludarabine phosphate (2-F-ara-AMP) is an adenine nucleoside analogue that shows significant activity against chronic lymphocytic leukemia and indolent lymphoma. We assessed the cytotoxic interaction produced by the combination of the active metabolite of fludarabine phosphate, fludarabine (9-β-D-arabinofuranosyl-2-fluoroadenine, 2-F-ara-A), and some commonly used antileukemic agents against human hairy cell leukemia cell line JOK-1, human chronic lymphocytic leukemia cell line SKW-3, and adult T cell leukemia cell lines ED-40810 (−) and SALT-3. The leukemia cells were exposed simultaneously to 2-F-ara-A and to the other agents for 4 days. Cell growth inhibition was determined using MTT reduction assay. The isobologram method of Steel and Peckham was used to evaluate the cytotoxic interaction. 2-F-ara-A and cytarabine showed synergistic effects in SKW-3 cells, additive and synergistic effects in JOK-1 and SALT-3 cells, and additive effects in ED-40810(−) cells. 2-F-ara-A and doxorubicin showed additive effects in SKW-3, ED-40810(−) and SALT-3 cell lines, and additive and synergistic effects in JOK-1 cells. 2-F-ara-A showed additive effects with etoposide, 4-hydroperoxy-cyclophosphamide, and hydroxyurea in all four cell lines. 2-F-ara-A showed antagonistic effects with methotrexate and vincristine in all four cell lines. Our findings suggest that the simultaneous administration of fludarabine phosphate with cytarabine, doxorubicin, etoposide, cyclophosphamide, or hydroxyurea would be advantageous for cytotoxic effects. Among these agents, cytarabine may be the best agent for the combination with fludarabine phosphate. The simultaneous administration of fludarabine phosphate with methotrexate or vincristine would have little cytotoxic effect, and this combination may be inappropriate. These findings may be useful in clinical trials of combination chemotherapy with fludarabine phosphate and these agents.Keywords
This publication has 36 references indexed in Scilit:
- Combined therapy with Fludarabine and Cyclophosphamide in relapsed/resistant patients with B‐cell chronic lymphocytic leukaemia and non‐Hodgkin's lymphomasEuropean Journal of Haematology, 1997
- Inhibition of the 3′→ 5′ Exonuclease of Human DNA Polymerase ε by Fludarabine-terminated DNAJournal of Biological Chemistry, 1996
- Non-Hodgkin's lymphomas—current status of therapy and future perspectivesEuropean Journal Of Cancer, 1995
- A Novel Adult T Cell Leukemia-Derived Cell Line (SALT-3) Susceptible to Human Immunodeficiency Virus Type 1 Infection.The Kurume Medical Journal, 1995
- p53 Status and the Efficacy of Cancer Therapy in VivoScience, 1994
- Effects of CPT‐11 in combination with other anti‐cancer agents in cultureInternational Journal of Cancer, 1992
- Phase I Clinical Investigation of Fludarabine Phosphate by a Loading-Dose and Continuous-Infusion ScheduleJNCI Journal of the National Cancer Institute, 1988
- Deregulation of c- myc by Translocation of the α-Locus of the T-Cell Receptor in T-Cell LeukemiasScience, 1986
- Origin of human T-lymphotrophic virus I-positive T cell lines in adult T cell leukemia. Analysis of T cell receptor gene rearrangement.The Journal of Experimental Medicine, 1985
- Glucocorticoid receptors in hairy-cell leukemiaInternational Journal of Cancer, 1982