1 alpha,25-Dihydroxyvitamin D-3 and its analogues, EB1089 and CB1093, profoundly inhibit the in vitro proliferation of the human hepatoblastoma cell line HepG2

Background: 1 alpha ,25-dihydroxyvitamin D-3 (1,25[OH](2)D-3) has been show n to inhibit the proliferation of various cancer cells including colon, pro state, melanoma, osteosarcoma and breast cancer. Methods: The human hepatoma cell line (HepG2) was cultured with 1,25(OH)(2) D-3 or one of two analogues EB1089 or CB1093 for various durations. Cellula r proliferation was measured by uptake of [H-3]thymidine, and cell numbers were determined by trypan blue exclusion counting. Results: 1,25(OH)(2)D-3, EB1089 and CB1093 all inhibited proliferation of H epG2 by up to 90% after 5 days of treatment, compared to the untreated cont rols. Decreased proliferation was associated with an approximately 50% redu ction in cell numbers at concentrations of up to 10(-10) mol/L after 5 days of treatment with 1,25(OH)(2)D-3. Cell proliferation rapidly recovered in cultures treated with lower concentrations of 1,25(OH)(2)D-3 (10(-10) and 1 0(-11) mol/L) when 1,25(OH)(2)D-3 was removed from the cultures by placing cells in serum containing medium without 1,25(OH)(2)D-3. When HepG2 cells w ere treated with 10(-8) mol/L 1,25(OH)(2)D-3 for 5 weeks, there was still s ignificant inhibition of proliferation, although at week 5 there was 66% in hibition compared to 93% at the end of week 1. Conclusions: 1,25(OH)(2)D-3, EB1089 and CB1093 all significantly inhibit th e proliferation of HepG2 hepatoblastoma cells, with EB1089 being the most p otent at lower concentrations. Inhibition can be maintained for at least 4 weeks, but is reversed after removal of vitamin D-3.