Abstract: | Objective: To explore the growth inhibition effects and apoptosis inducing mechanisms of curcumin on human ovarian cancer cell line
A2780.Methods: After treatment with 10–50 μmol/L curcumin for 6–24 h, the growth activity of A2780 cancer cells were studied by 4,5-dimethylthiazol-2-yl]-2,
5-dipheny-Itetrazolium bromide (MTT) colorimetry. Cellular apoptosis was inspected by flow cytometery and acridine orange-ethidium
bromide fluorescent staining methods. The fragmentation of cellular chromosome DNA was detected by DNA ladder, the ultrastructural
change was observed under a transmission electron microscope, and the protein levels of nuclear factor-Kappa B (NF-κB, P65)
and cysteinyl aspartate specific protease-3 (Caspase-3) in ovarian cancer cells were measured by immunohistochemistry.Results: After treatment with various concentrations of curcumin, the growth inhibition rates of cancer cells reached 62.05% —89.
24%, with sub-G1 peaks appearing on histogram. Part of the cancer cells showed characteristic morphological changes of apoptosis under fluorescence
and electron microscopes, and the rate of apoptosis was 21.5%–33.5%. The protein expression of NF-κB was decreased, while
that of Caspase-3 was increased in a time-dependent manner.Conclusion: Curcumin could significantly inhibit the growth of human ovarian cancer cells; inducing apoptosis through up-regulating
Caspase-3 and down-regulating gene expression of NF-κB is probably one of its molecular mechanisms.
Supported by National Natural Science Foundation of China (No. 30200284) |