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

We determined the potential activity of 2',2'-difluorodeoxycytidine (gemcit abine, dFdC) in 1-beta-D arabinofuranosylcytidine (ara-C)-sensitive and-res istant leukemia cell lines. Both drugs are phosphorylated by deoxycytidine kinase (dCK); the triphosphates, dFdCTP and ara CTP, respectively, are inco rporated into DNA. In the murine leukemia cell line L1210, induction of res istance to ara-C resulted in the 2200-fold resistant subline L4A6. The Brow n 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, gemci tabine 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, resp ectively. A partial explanation for these differences may be the higher dCK activity in the parental cell lines L1210 and BCLO with gemcitabine compar ed to ara-C as a substrate. DCK activity was not or hardly detectable in th e resistant L4A6 and Bara-C cell. In the rat leukemia cell lines, deoxycyti dine (dCyd) phosphorylation activity showed an aberrant pattern, since the activity with dCyd was 1.5-fold higher in the Bara-C cell line compared wit h BCLO, possibly due to thymidine kinase 2. The wild-type L1210 cells accum ulated at least 3-fold more ara-CTP and dFdCTP than the rat leukemia cell l ine BCLO. The ara-C-resistant variants L4A6 and Bara C did not accumulate d FdCTP 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. (C) 1999 Elsevier Sc ience Inc.