Anti proliferative activity of ELACYT™ (CP-4055) in combination with cloretazine (VNP40101M), idarubicin, gemcitabine, irinotecan an topotecan in human leukemia and lymphoma cells

David J. Adams*, Marit L. Sandvold, Finn Myhren, Tove F. Jacobsen, Frank Giles, David A. Rizzieri

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

This study evaluated combination drug partners for CP-4055, the C18:1Δ9,trans unsaturated fatty acid ester of cytarabine in HL-60 and U937 cells. Growth inhibition was assessed by ATP assay and drug interaction by the combination index and three dimensional methods. Synergy was observed in HL-60 cells for simultaneous combinations of CP-4055 with gemcitabine, irinotecan and topotecan, while combinations with cloretazine (VNP40101M) and idarubicin were additive. In U937 cells, synergy was observed with gemcitabine and additivity for the other drugs. In HL-60, the IC50 concentration of CP-4055 could be reduced 10-fold and that of gemcitabine 3-fold in combination versus the agents alone, an interaction that was independent of drug sequence, ratio and exposure time. In contrast, interactions of CP-4055 with the topoisomerase inhibitors became antagonistic when the drugs were administered 24 h prior to CP-4055 and at certain drug ratios, particularly in U937 cells. In summary, CP-4055 produced additive to synergistic anti proliferative activity when combined simultaneously with drugs from four mechanistic classes in cell culture models of human leukemia and lymphoma. The impact of drug sequence and ratio on the interactions argues for incorporation of these parameters into the design of combination chemotherapy regimens.

Original languageEnglish (US)
Pages (from-to)786-797
Number of pages12
JournalLeukemia and Lymphoma
Volume49
Issue number4
DOIs
StatePublished - Apr 2008

Keywords

  • Combination chemotherapy
  • DNA antimetabolite
  • Drug synergy
  • Leukemia
  • Lymphoma
  • Median effect analysis

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

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