Different modes of transport for ³H-thymidine, ³H-FLT, and ³H-FMAU in proliferating and nonproliferating human tumor cells

The basis for the use of nucleoside tracers in PET is that activity of the cell-growth-dependent enzyme thymidine kinase 1 is the rate-limiting factor driving tracer retention in tumors. Recent publications suggest that nucleoside transporters might influence uptake and thereby affect the tracer signal in vivo. Understanding transport mechanisms for different nucleoside PET tracers is important for evaluating clinical results. This study examined the relative role of different nucleoside transport mechanisms in uptake and retention of [methyl-³H]-3′-deoxy-3′-fluorothymidine ( ³H-FLT), [methyl-³H]-thymidine (³H-thymidine), and ³H-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-5-methyluracil (³H-FMAU). Methods: Transport of ³H-FLT, ³H-thymidine, and ³H-FMAU was examined in a single human adenocarcinoma cell line, A549, under both nongrowth and exponential-growth conditions. Results: ³H-Thymidine transport was dominated by human equilibrative nucleoside transporter 1 (hENT1) under both growth conditions. ³H-FLT was also transported by hENT1, but passive diffusion dominated its transport. ³H-FMAU transport was dominated by human equilibrative nucleoside transporter 2. Cell membrane levels of hENT1 increased in cells under exponential growth, and this increase was associated with a more rapid rate of uptake for both ³H-thymidine and ³H-FLT. ³H-FMAU transport was not affected by changes in growth conditions. All 3 tracers concentrated in the plateau phase, nonproliferating cells at levels many-fold greater than their concentration in buffer, in part because of low levels of nucleoside metabolism, which inhibited tracer efflux. Conclusion: Transport mechanisms are not the same for ³H-thymidine, ³H-FLT, and ³H-FMAU. Levels of hENT1, an important transporter of ³H-FLT and ³H-thymidine, increase as proliferating cells enter the cell cycle. COPYRIGHT