Decreased resistance to gemcitabine (2',2'-difluorodeoxycitidine) of cytosine arabinoside-resistant myeloblastic murine and rat leukemia cell lines: role of altered activity and substrate specificity of deoxycytidine kinase

Biochem Pharmacol. 1999 Feb 15;57(4):397-406. doi: 10.1016/s0006-2952(98)00318-9.


We determined the potential activity of 2',2'-difluorodeoxycytidine (gemcitabine, dFdC) in 1-beta-D-arabinofuranosylcytidine (ara-C)-sensitive and-resistant leukemia cell lines. Both drugs are phosphorylated by deoxycytidine kinase (dCK); the triphosphates, dFdCTP and ara-CTP, respectively, are incorporated into DNA. In the murine leukemia cell line L1210, induction of resistance to ara-C resulted in the 2200-fold resistant subline L4A6. The Brown Norway rat myelocytic leukemia ara-C-sensitive cell line (BCLO) was >300-fold more sensitive to ara-C than its variant Bara-C. In L1210 cells, gemcitabine was 8-fold more active than ara-C; in L4A6, BCLO, and Bara-C cells, gemcitabine was 16-, 28-, and more than 3-fold more active than ara-C, respectively. A partial explanation for these differences may be the higher dCK activity in the parental cell lines L1210 and BCLO with gemcitabine compared to ara-C as a substrate. DCK activity was not or hardly detectable in the resistant L4A6 and Bara-C cell. In the rat leukemia cell lines, deoxycytidine (dCyd) phosphorylation activity showed an aberrant pattern, since the activity with dCyd was 1.5-fold higher in the Bara-C cell line compared with BCLO, possibly due to thymidine kinase 2. The wild-type L1210 cells accumulated at least 3-fold more ara-CTP and dFdCTP than the rat leukemia cell line BCLO. The ara-C-resistant variants L4A6 and Bara-C did not accumulate dFdCTP or ara-CTP. In conclusion, gemcitabine was more active than ara-C in all leukemia cell lines tested. The sensitivity of the wild-type cell lines correlates with the accumulation of dFdCTP and ara-CTP, but is independent of dCK. However, both resistant variants had decreased dCK activities, but were relatively more sensitive to dFdC than to ara-C.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimetabolites, Antineoplastic / pharmacology*
  • Cell Division / drug effects
  • Cytarabine / metabolism*
  • Cytarabine / pharmacology
  • Cytidine Deaminase
  • DNA / biosynthesis
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Deoxycytidine Kinase / metabolism*
  • Drug Resistance / genetics
  • Leukemia L1210 / genetics
  • Leukemia L1210 / metabolism
  • Mice
  • Nucleoside Deaminases / metabolism
  • Polyphosphates / analysis
  • Rats
  • Rats, Inbred BN
  • Substrate Specificity
  • Thymidine Kinase / metabolism
  • Tumor Cells, Cultured


  • Antimetabolites, Antineoplastic
  • Polyphosphates
  • Cytarabine
  • Deoxycytidine
  • DNA
  • gemcitabine
  • Thymidine Kinase
  • Deoxycytidine Kinase
  • Nucleoside Deaminases
  • Cytidine Deaminase
  • deoxycytidine deaminase
  • triphosphoric acid