Transport mechanisms of trans-1-amino-3-fluoro[1-14C]cyclobutanecarboxylic acid in prostate cancer cells

Introduction: We investigated the mechanisms of trans-1-amino-3-fluoro[1-14C]cyclobutanecarboxylic acid (anti-[14C]FACBC) transport by human-derived prostate cancer (PCa) cells and normal human prostatic epithelial cells (PrECs). Methods: Using PCa cells (DU145, PC-3, LNCaP) and PrECs, we performed the following in vitro experiments: time-course, kinetics, competitive inhibition by synthetic/naturally occurring amino acids (AAs), exchange transport with synthetic/naturally occurring AAs and pH-dependency of anti-[14C]FACBC uptake. We also examined the amino acid transporter (AAT) expression using flow cytometry. Results: The uptake of anti-[14C]FACBC by LNCaP and DU145 cells was higher than that by PC-3 and PrECs. The Km values for anti-[14C]FACBC were 64.4 and 191.7 μmol/L in the DU145 cells and PrECs, respectively. Total levels of anti-[14C]FACBC uptake were positively correlated with the expression level of system ASC in PCa cells. The contributions of Na+-dependent AATs to anti-[14C]FACBC uptake were greater than those of Na+-independent AATs, especially in PCa cells. In the presence of Na+, glutamine and serine showed the strongest inhibitory effect against anti-[14C]FACBC uptake, suggesting that system ASC, especially ASCT2, is an important AAT for anti-[14C]FACBC. In contrast, phenylalanine and 2-amino-bicyclo[2,2,1]heptane-2-carboxylic acid, but not N-ethylmaleimide, almost completely inhibited the anti-[14C]FACBC uptake in the absence of Na+, indicating the contribution of LAT1. In the exchange transport experiments, glutamine showed the strongest transstimulation of intracellular anti-[14C]FACBC efflux in DU145 cells. Furthermore, the contributions of Na+-independent AATs to the uptake of anti-[14C]FACBC in DU145 and PrECs were greater under acidic pH conditions than under neutral or alkaline pH conditions. Conclusions: Total uptake of anti-[14C]FACBC by PCa cells correlates with the expression level of system ASC in PCa cells. Furthermore, LAT1 is an important transport system for anti-[14C]FACBC uptake, especially in an acidic environment, such as the intra-tumoural environment.