Troglitazone, a peroxisome proliferator-activated receptor γ ligand, induces growth inhibition and apoptosis of HepG2 human liver cancer cells

AIM： To examine the effect of troglitazone, a peroxisome proliferator-activated receptor γ （PPARγ） ligand, on the proliferation and apoptosis of human liver cancer cells. METHODS： Liver cancer cell line HepG2 was cultured and treated with troglitazone. Cell proliferation was detected by 3-（4-,5-dimethylthiazol-2-yl）-2,5-diphenyl tetrazolium bromide （MTT） assay; apoptosis was detected by flow cytometry and terminal deoxynucleotidyl transferase- mediated nick end labeling of DNA fragmentation sites （TUNEL） assay; and apoptosis-related protein was detected by immunocytochemistry and Western blotting. RESULTS： Troglitazone inhibited growth and induced apoptosis of HepG2 cells in a dose-dependent manner, and induced activation of caspase-3 expression. Troglitazone not only drove apoptosis-inhibiting factor survivin to translocate incompletely from the nucleus to the cytoplasm, but also inhibited expression of survivin, while it did not affect expression of apoptosis-promoting factor Bax. CONCLUSION： PPARγ ligands inhibit growth and induce apoptosis of liver cancer cells, and may have applications for the prevention and treatment of liver cancer.