Gemcitabine transport in Xenopus Oocytes expressing recombinant plasma membrane mammalian nucleoside transporters

• Published in: JNCI : Journal of the National Cancer Institute Vol. 91; no. 21; pp. 1876 - 1881
• Main Authors: MACKEY, J. R, YAO, S. Y. M, SMITH, K. M, KARPINSKI, E, BALDWIN, S. A, CASS, C. E, YOUNG, J. D
• Format: Journal Article
• Language: English
• Published: Cary, NC Oxford University Press 03.11.1999; Oxford Publishing Limited (England)
• Subjects: Animals; Antimetabolites, Antineoplastic - metabolism; Antimetabolites, Antineoplastic - pharmacology; Antineoplastic agents; Biological and medical sciences; Biological Transport; Cancer; Carrier Proteins - genetics; Carrier Proteins - metabolism; Cell Membrane - metabolism; Chemotherapy; Deoxycytidine - analogs & derivatives; Deoxycytidine - metabolism; Deoxycytidine - pharmacology; Electrophysiology; Medical sciences; Membrane Proteins - metabolism; Membranes; Neoplasms - drug therapy; Neoplasms - metabolism; Nucleosides - metabolism; Oocytes - metabolism; Pharmacology. Drug treatments; Plasma; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; Sodium Channels - drug effects; Studies; Tumors; Uridine - metabolism; Xenopus laevis; Antineoplastic agent; Gemcitabine; Xenopus laevis; Amphibia; Salientia; Vertebrata; Antimetabolic; Membrane transport; Animal; Plasma membrane; Nucleoside; Fluorine Organic compounds; Pharmacokinetics; Pyrimidine nucleoside; Oocyte; Carrier protein
• ISSN: 0027-8874; 1460-2105
• DOI: 10.1093/jnci/91.21.1876

Gemcitabine, a pyrimidine analogue of deoxycytidine, is an anticancer nucleoside drug that requires functional plasma membrane nucleoside transporter proteins to reach its intracellular targets and cause cytotoxicity. Because of technical difficulties inherent in studying nucleoside transport in human cells, we rigorously defined gemcitabine membrane transportability by producing each of the available human (h) and rat (r) recombinant nucleoside transporters (NTs) individually in Xenopus laevis oocytes. Oocytes were microinjected with in vitro-transcribed RNAs derived from complementary DNAs encoding (C = concentrative) rCNT1, rCNT2, hCNT1, hCNT2, (E = equilibrative) rENT1, rENT2, hENT1, and hENT2. Uptake of [(3)H]gemcitabine and [(14)C] uridine was measured 3 days after microinjection to determine kinetic constants. We also used the two-electrode, voltage-clamp technique to investigate the electrophysiology of hCNT1-mediated gemcitabine transport. Gemcitabine was transported by most of the tested proteins (the exceptions being the purine-selective rCNT2 and hCNT2), with the greatest uptake occurring in oocytes producing recombinant rCNT1 and hCNT1. Influxes of gemcitabine mediated by hCNT1, hENT1, and hENT2 were saturable and conformed to Michaelis-Menten kinetics with apparent K(m) values of 24, 160, and 740 microM, respectively. Gemcitabine had a limited ability to cross the lipid bilayer of oocyte membranes by simple diffusion. External application of gemcitabine to oocytes producing recombinant hCNT1 induced an inward current, which demonstrated that hCNT1 functions as a Na(+)/nucleoside co-transport protein and confirmed the transporter's ability to transport gemcitabine. Mammalian nucleoside transporters vary widely in their affinity and capacity to transport gemcitabine. Variation in the tumor and tissue distribution of plasma membrane nucleoside transporter proteins may contribute to the solid tumor activities and schedule-dependent toxic effects of gemcitabine.