Modulation of cytarabine induced cytotoxicity using novel deoxynucleoside analogs in the HL60 cell line

Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1513-6. doi: 10.1081/NCN-200027727.

Abstract

In order to enhance the cytotoxicity of ara-C in the HL60 cell line the following deoxynucleoside analogs were used: cladribine, fludarabine and gemcitabine. HL60 cells were co-incubated with ara-C and each of the modulators at the ratios of their respective IC50s. Cytotoxicity was determined with the MTT-assay and drug interactions were evaluated with the combination index (CI) method (Calcusyn; Chou & Talalay). CI < 1, CI +/- 1 and > 1 indicate synergism, additive effect and antagonism, respectively. We observed moderate synergism between ara-C/cladribine and ara-C/gemcitabine, with CIs of 0.76 +/- 0.14 and 0.82 +/- 0.04, respectively. The interaction between ara-C/fludarabine resulted in moderate antagonism (CI = 1.29 +/- 0.11). In conclusion, in this in vitro study we showed that the cytotoxicity of ara-C can be succesfully modulated in the HL60 cell line by cladribine and gemcitabine.

MeSH terms

  • Antimetabolites, Antineoplastic / pharmacology*
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cladribine / pharmacology
  • Coloring Agents / pharmacology
  • Cytarabine / pharmacology*
  • DNA / metabolism
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Gemcitabine
  • HL-60 Cells
  • Humans
  • Inhibitory Concentration 50
  • Nucleosides / chemistry*
  • Tetrazolium Salts / pharmacology
  • Thiazoles / pharmacology
  • Vidarabine / analogs & derivatives*
  • Vidarabine / pharmacology

Substances

  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Coloring Agents
  • Nucleosides
  • Tetrazolium Salts
  • Thiazoles
  • Cytarabine
  • Deoxycytidine
  • Cladribine
  • DNA
  • thiazolyl blue
  • Vidarabine
  • fludarabine
  • Gemcitabine