We have assessed the response of a previously characterized multidrug resistant (MDR) human
erythroleukemia cell line (K562R) to the
nucleoside analog antimetabolite 1-beta-D-arabinofuranosylcytosine (
ara-C). This cell line has been subjected to selection pressure by intermittent exposure to
daunorubicin, but not
ara-C, since its initial isolation. In comparison to the parental line (K562S), K562R were approximately 15-fold more resistant to
ara-C as determined by 3H-dThd incorporation, MTT
dye reduction and clonogenicity. Following a 4-h exposure to 10 microM
ara-C, K562S accumulated approximately seven times more
ara-CTP, and incorporated approximately 250% more
ara-C into
DNA than their resistant counterparts. The intracellular generation of
ara-CTP was not significantly influenced by the
cytidine deaminase inhibitor THU or the
deoxycytidylate deaminase inhibitor dTHU (1 mM each) in either cell line. Rates of dephosphorylation of
ara-CTP were equivalent in sensitive and resistant cells, as were intracellular levels of both
ribonucleotide and
deoxyribonucleotide triphosphates. However, K562R displayed a significant (ie 70%) reduction in the level of activity of the
pyrimidine salvage pathway
enzyme,
deoxycytidine kinase (dCK), compared to K562S cells. In contrast to U937 leukemic cells,
DNA extracted from K562S and K562R cells following exposure to 10 microM
ara-C for 6 h did not exhibit the characteristic internucleosomal DNA cleavage on
agarose gel electrophoresis typical of
drug-induced apoptosis. Lastly, Northern analysis revealed equivalent levels of dCK message in the two cell lines. K562R represents an unusual example of a classical multidrug resistant human leukemic cell line exhibiting spontaneous cross-resistance to the
antimetabolite ara-C, and may prove of value in attempts to understand the mechanism(s) by which human leukemic myeloblasts survive in vivo exposure to combination chemotherapeutic regimens containing drugs that are not classically associated with the multidrug resistance phenomenon.