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Japanese Journal of Cancer Research : Gann logoLink to Japanese Journal of Cancer Research : Gann
. 1999 Jul;90(7):781–787. doi: 10.1111/j.1349-7006.1999.tb00815.x

Contribution of the Nucleoside Transport System to Doxorubicin Transport in HL60 Cells but Not in Mononuclear Cells

Kazuki Nagasawa 1, Tomohiko Fumihara 1, Noriaki Ohnishi 1, Teruyoshi Yokoyama 1,
PMCID: PMC5926127  PMID: 10470292

Abstract

Previously, we reported that pirarubicin (THP), an anthracycline, was transported, at least in part, via a nucleoside transport system in human leukemic HL60 cells, but not in mononuclear cells (MNCs). In this study, the contribution of the nucleoside transport system to the transport of other anthracyclines, doxorubicin (DOX), daunorubicin (DNR) and idarubicin (IDA), in HL60 cells and MNCs was investigated. The experiments were performed after both types of cells had been pretreated with a metabolic inhibitor, 2,4‐dinitrophenol, to deplete cellular ATP. The DOX uptake by HL60 cells was partially inhibited by inhibitors of equilibrative nucleoside transporters. In HL60 cells, moreover, the uptake of DOX depended on an inwardly directed Na+‐gradient, and was inhibited by concentrative nucleoside transporters, but there was no change in the DNR or IDA uptake under any of these conditions. On the other hand, the uptake of the three drugs by MNCs was not affected by any inhibitors of the nucleoside transporters, and there was no dependence of the uptake on an Na+‐gradient. These results suggested that DOX, but not DNR or IDA, was partially transported in HL60 cells via the nucleoside transport system, whereas in MNCs the system did not contribute to the uptake of any of these three drugs. Thus, nucleoside transport systems contributing to the transport of anthracyclines may be different among different derivatives and cell types.

Keywords: Anthracycline, Transport mechanism, Nucleoside transport system, Human leukemia HL60 cell, Human mononuclear cell

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REFERENCES

  • 1).Nagasawa , K. , Natazuka , T. , Chihara , K. , Kitazawa , F. , Tsumura , A. , Takara , K. , Nomiyama , M. , Ohnishi , N. and Yokoyama , T.Transport mechanism of anthracycline derivatives in human leukemia cell lines: uptake and efflux of pirarubicin in HL60 and pirarubicin‐resistant HL60 cells . Cancer Chemother. Pharmacol. , 37 , 297 – 304 ( 1996. ). [DOI] [PubMed] [Google Scholar]
  • 2).Nagasawa , K. , Natazuka , T. , Nomiyama , M. , Ohnishi , N. and Yokoyama , T.Transport mechanism of anthracycline derivatives in human leukemia cell lines: uptake and efflux of daunorubicin and doxorubicin in HL60 and its resistant cells and comparison with those of pirarubicin . Biol. Pharm. Bull. , 19 , 100 – 105 ( 1996. ). [DOI] [PubMed] [Google Scholar]
  • 3).Nagasawa , K. , Tsumura , A. , Nomiyama , M. , Ohnishi , N. and Yokoyama , T.Transport mechanism of pirarubicin in human mononuclear cells . Biol. Pharm. Bull. , 19 , 1203 – 1209 ( 1996. ). [DOI] [PubMed] [Google Scholar]
  • 4).Nagasawa , K. , Ohnishi , N. and Yokoyama , T.Transport mechanisms of idarubicin, an anthracycline derivative, in human leukemia HL60 cells and mononuclear cells, and comparison with those of its analogs . Jpn. J. Cancer Res. , 88 , 750 – 759 ( 1997. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5).Nagasawa , K. , Ohnishi , N. and Yokoyama , T.Possibility of contribution of nucleoside transport systems to pirarubicin uptake by HL60 cells but not mononuclear cells . Jpn. J. Cancer Res. , 89 , 673 – 680 ( 1998. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6).Plagemann , P. G. W. and Wohlhueter , R. M.Permeation of nucleosides, nucleic acid bases, and nucleotides in animal cells . Curr. Top. Membr. Transp. , 14 , 225 – 330 ( 1980. ). [Google Scholar]
  • 7).Plagemann , P. G. W. , Wohlhueter , R. M. and Woffendin , C.Nucleoside and nucleobase transport in animal cells . Bio-chim. Biophys. Acta , 947 , 405 – 443 ( 1988. ). [DOI] [PubMed] [Google Scholar]
  • 8).Griffith , D. A. and Jarvis , S. M.Nucleoside and nucleobase transport systems of mammalian cells . Biochim. Biophys. Acta , 1286 , 153 – 181 ( 1996. ). [DOI] [PubMed] [Google Scholar]
  • 9).Wang , J. W. , Schaner , M. E. , Thomassen , S. , Su , S.‐F. , Piquette‐Miller , M. and Giacomini , K. M.Functional and molecular characteristics of Na+‐dependent nucleoside transporters . Pharm. Res. , 14 , 1524 – 1532 ( 1997. ). [DOI] [PubMed] [Google Scholar]
  • 10).Tarasiuk , J. , Foucrier , J. and Garnier‐Suillerot , A.Cell cycle dependent uptake and release of anthracycline by drug‐resistant and drug‐sensitive human leukemic K562 cells . Biochem. Pharmacol. , 45 , 1801 – 1808 ( 1993. ). [DOI] [PubMed] [Google Scholar]
  • 11).Barcelo , F. , Barcelo , I. , Ferragut , F. A. , Yanovich , S. and Gonzalez‐Ros , J. M.Interaction of anthracyclines with nucleotides and related compounds studied by spectroscopy . Biochim. Biophys. Acta , 884 , 172 – 181 ( 1986. ). [DOI] [PubMed] [Google Scholar]
  • 12).Crawford , C. R. , Ng , C. Y. C. , Noel , D. and Belt , J. A.Nucleoside transport in L1210 murine leukemia cells. J . Biol. Chem. , 265 , 9732 – 9736 ( 1990. ). [PubMed] [Google Scholar]
  • 13).Cai , J. and Lee , C. W.Tamoxifen inhibits nitrobenzylthioino sine‐sensitive equilibrative uridine transport in human MCF‐7 breast cancer cells . Biochem. J. , 320 , 991 – 995 ( 1996. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14).Plagemann , P. G. W. and Woffendin , C.Species differences in sensitivity of nucleoside transport in erythrocytes and cultured cells to inhibition by nitrobenzylthioinosine, dipyridamole, dilazep and lidoflazine . Biochim. Biophys. Acta , 969 , 1 – 8 ( 1988. ). [DOI] [PubMed] [Google Scholar]
  • 15).Dutcher , J. P. , Wiernik , P. H. , Markus , S. , Weinberg , V. , Schiffer , C. A. and Harwood , K. V.Intensive maintenance therapy improves survival in adult acute nonlymphocytic leukemia: an eight‐year follow‐up . Leukemia , 7 , 413 – 419 ( 1988. ). [PubMed] [Google Scholar]
  • 16).Yates , J. W. , Glidewell , O. , Wiernik , P. H. , Cooper , M. R. , Steinberg , D. , Dosik , H. , Levy , R. , Hoagland , C. , Henry , P. , Gottleib , A. , Cornell , C. , Berenberg , J. , Hutchison , J. L. , Raich , P. , Nissen , N. , Ellison , R. R. , Frelick , R. , James , G. W. , Falkson , G. , Silver , R. T. , Haurani , F. , Green , M. , Henderson , E. , Leone , L. and Holland , J. F.Cytosine arabinoside with daunorubicin or adriamycin for therapy of acute myelocytic leukemia: a CALGB study . Blood , 60 , 454 – 462 ( 1982. ). [PubMed] [Google Scholar]
  • 17).van Sloten , K. , Wiernik , P. H. , Schiffer , C. A. and Schimpff , S. C.Evaluation of levamisole as an adjuvant to chemotherapy for treatment of ANLL . Cancer , 51 , 1576 – 1580 ( 1983. ). [DOI] [PubMed] [Google Scholar]
  • 18).Yates , J. W. , Wallace , H. R. , Ellison , R. R. and Holland , J. F.Cytosine arabinoside (NSC‐63878) and daunorubicin (NSC‐83142) therapy in acute nonlymphocytic leukemia . Cancer Chemother. Rep. , 57 , 485 – 488 ( 1973. ). [PubMed] [Google Scholar]
  • 19).Goh , L.‐B. , Mack , P. and Lee , C.‐W.Nitrobenzylthio‐inosine‐binding protein overexpression in human breast, liver, stomach and colorectal tumour tissues . Anticancer Res. , 15 , 2575 – 2580 ( 1995. ). [PubMed] [Google Scholar]
  • 20).Deckert , J. , Morgan , P. F. and Marangos , P. J.Adenosine uptake site heterogeneity in the mammalian CNS? Uptake inhibitors as probes and potential neuropharmaceuticals . Life Sci. , 42 , 1331 – 1345 ( 1988. ). [DOI] [PubMed] [Google Scholar]
  • 21).Jones , K. W. and Hammond , J. R.Heterogeneity of [3H]dipyridamole binding to CNS membranes: correlation with [3H]nitrobenzylthioinosine binding and [3H]uridine influx studies . J. Neurochem. , 59 , 1363 – 1371 ( 1992. ). [DOI] [PubMed] [Google Scholar]
  • 22).Williams , E. F.Chronic dipyridamole administration downregulates [3H]nitrobenzylthioinosine binding site affinity in guinea pig kidney but not heart and brain . Life Sci. , 59 , 2051 – 2057 ( 1996. ). [DOI] [PubMed] [Google Scholar]

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