Table I.
β-Elemene increases cisplatin cytotoxicity and enhances cisplatin sensitivity in human ovarian carcinoma cells, as determined by MTT assay.
IC50 | ||||
---|---|---|---|---|
|
||||
Drug | 24 h | 48 h | 72 h | 96 h |
A2780 cells | ||||
β-Elemene (μg/ml) | 65 | 65 | 65 | 60 |
Cisplatin (μM) | 6.2 | 1.75 | 1.6 | 1.5 |
β-Elemene + cisplatin (μM) | 3.8 | 0.8 | 0.75 | 0.6 |
Dose-modifying factor | 1.6 | 2.2 | 2.1 | 2.5 |
A2780/CP70 cells | ||||
β-Elemene (μg/ml) | 80 | 70 | 68 | 65 |
Cisplatin (μM) | 95 | 66 | 65 | 60 |
β-Elemene + cisplatin (μM) | 2.5 | 1.9 | 1.85 | 1.0 |
Dose-modifying factor | 38 | 34.7 | 35.1 | 60 |
The results reveal that β-elemene increased cisplatin cytotoxicity by 34.7- to 60-fold in A2780/CP70 cells, but only 1.6- to 2.5-fold in A2780 cells. The IC50 (half maximal inhibitory concentration) value is defined as the concentration of β-elemene or cisplatin needed for 50% inhibition of cell growth and proliferation. The dose-modifying factor (DMF) was calculated as the IC50 for cisplatin without β-elemene divided by the IC50 for cisplatin with β-elemene: DMF = IC50 (cisplatin) ÷ IC50 (cisplatin + β-elemene). MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide.