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. 2013 Jun 28;43(3):721–728. doi: 10.3892/ijo.2013.1996

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.