Biochemical Pharmacology. 2008 May 15;75(10):1901-11. Epub 2008 Feb 16. [Link]
Damaraju D, Damaraju VL, Brun M, Mowles D, Kuzma M, Berendt RC, Sawyer MB, Cass CE.
Department of Oncology, University of Alberta, Alberta, Canada.
This study was designed to evaluate the cytotoxic activity of several nucleoside and nucleobase analog drugs as possible new agents for treatment of malignant mesothelioma and to identify factors responsible for the clinical variation of nucleoside analog drug response in chemotherapy of mesothelioma. Three human mesothelioma cell lines (MSTO-211H, H2452 and H2052) were tested for gemcitabine sensitivity and nucleoside transport activity. MSTO-211H, H2452 and H2052 exhibited differences in sensitivity to gemcitabine, nucleoside transport rates and hENT1 site densities. In H2052 cells, gemcitabine, 5-fluoro-2â€²-deoxyuridine, clofarabine and cladribine were most active with IC50 values of 46, 43, 240 and 490 nM, respectively, whereas 5-fluorouracil was the least cytotoxic drug tested. In H2052 cells, the combination of gemcitabine and fludarabine or cladribine resulted in synergistic cytotoxic response. In nucleobase transport studies, hypoxanthine and 6-mercaptopurine but not 5-fluorouracil was transported into H2052 cells by a novel purine-specific, sodium-independent nucleobase transport activity. In summary differences in nucleoside analog drug transport activities are likely to contribute to the observed clinical variation in nucleoside analog response in patients and for the first time a correlation between nucleobase drug sensitivities and transport activities was shown. A novel combination of gemcitabine and fludarabine or cladribine had synergistic cytotoxic activity against the least sensitive mesothelioma cell line. These drug combinations merit further evaluation as effective therapeutic regimens in patients with aggressive mesothelioma.
Keywords: Mesothelioma; Nucleosides; Nucleobases; Gemcitabine; Synergy; hENT1
Abbreviations: hENT, human equilibrative nucleoside transporter; NBMPR, nitrobenzylmercaptopurine riboside; IC50, the concentration of drug that inhibited growth of treated cells by 50% relative to that of untreated cells; Cl-dAdo, cladribine; Fara-A, fludarabine; 5-FU, 5-fluorouracil; 6-MP, 6-mercaptopurine; CI, combination index