Fig. 6

a Huh-7 cells were transfected with hAxin-1017 and C/EBP-β expression plasmid and pRL-CMV plasmid. After 48 h, luciferase activities were measured. b–f Huh-7 cells were incubated with the vehicle (DMSO) or thapsigargin (1 μM or indicated concentration) for 15 h. Whole-cell lysates prepared from Huh-7 cells were subjected to western blot analysis against the indicated antibodies (b). Real-time PCR for Axin1 and C/EBP-β were performed using total RNA prepared from Huh-7 cells (c). Chromatin samples were prepared and subsequently subjected to ChIP analysis against the anti-C/EBP-β antibody or control IgG. The amounts of immunoprecipitated C/EBP-β promoter regions were quantified by real-time PCR (d). Cytosolic proteins were subjected to western blot analysis against the β-catenin antibody (e) and total RNA was subjected to real-time PCR for β-catenin expression (f). g SNU475 cells were treated for 15 h with thapsigargin and cytosolic proteins were subsequently analyzed by western blot analysis against the β-catenin antibody. h Effect of thapsigargin on zebrafish embryonic development. i Lysates prepared from Huh-7 cells treated for 15 h with the vehicle (DMSO) or thapsigargin (1 μM) were subjected to western blot analysis against the indicated antibodies. j Effect of thapsigargin on hepatoma cell growth. In a–c, d, f, and j, results are the average of three experiments, and bars indicate standard deviations. *P < 0.05, compared with the control