Effects of alantolactone on cell proliferation and apoptosis of acute myeloid leukemia THP-1 cells / 白血病·淋巴瘤

ABSTRACT

Objective:To explore the effects of alantolactone on cell proliferation and apoptosis of acute myeloid leukemia cell line THP-1 and the related mechanisms.Methods:THP-1 cells in logarithmic growth phase were taken. The control group was added with an equal volume of culture medium containing 10% fetal bovine serum, and the experimental group was added with 0.5, 1.0, 2.0, 4.0, 6.0, 8.0, 10.0 μmol/L alantolactone. The cells in each group were cultured for 72 hours. The cell proliferation was detected by CCK-8 method. In addition, the cells of the control group were taken, and the experimental group was added with 2.0 and 4.0 μmol/L alantolactone, respectively. The cells in each group were cultured for 72 hours. The apoptosis of the cells was detected by flow cytometry, and the expressions of NF-κB pathway-related proteins were detected by Western blotting.Results:After THP-1 cells were treated with different concentrations of alantolactone (0.5, 1.0, 2.0, 4.0, 6.0, 8.0, 10.0 μmol/L) for 72 hours, the inhibitory rates were (9.4±1.4)%, (27.7±4.0)%, (45.1±2.5)%, (66.9±2.9)%, (87.0±1.2)%, (91.7±1.0)% and (94.4±0.8)%, respectively, which were in a dose-dependent manner, and the control group was (0.4±0.1)%, the difference was statistically significant ( F = 241.87, P < 0.01). After THP-1 cells were treated with different concentrations of alantolactone (2.0, 4.0 μmol/L) for 72 hours, the apoptotic rates were (26.1±4.2)% and (37.8±5.6)%, and the control group was (8.5±1.4)%, the difference was statistically significant ( F = 43.04, P < 0.05). Furthermore, alantolactone could down-regulate the expression levels of bcl-2 and p65, and up-regulate the expression levels of bax, cleaved-caspase-3 and cleaved-PARP. Conclusions:Alantolactone can induce the apoptosis of AML THP-1 cells via inhibiting the NF-κB pathway, thereby inhibiting its proliferation.