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. 2018 Oct 12;41(1):178–190. doi: 10.3892/or.2018.6790

Table III.

Cytotoxicity induced by CPA or IFA alone or in combination with 2-ME.

O2 (%) 2-ME CPA CPA+2-ME R index Effect
16.2 94.35±7.3 56.8±1.7a 54.2±3.3 0.99±0.06 No effect
1 95.6±7.0 54.3±1.9a 27.3±2.1b 1.92±0.13c Additivity
0.1 93.2±3.0 55.5±1.5a 30.2±2.1b 1.74±0.11c Additivity

2-ME IFA IFA+2-ME R index Effect

16.2 93.9±1.0 53.7±2.2a 48.6±2.0 1.04±0.02 No effect
1 94.4±1.2 49.7±2.5a 23.6±2.3b 2.03±0.12c Synergy
0.1 95.4±1.6 48.8±2.9a 26.5±1.9b 1.77±0.10c Additivity

Cells were incubated for 24 h under normoxia (16.2% O2) or hypoxia (1 or 0.1% O2) with CPA or IFA in the absence and the presence of 2-ME (5 µM) and cell viability was determined with the MTT assay. Values are expressed as the percentage of the control cell viability (no drugs added) and are means ± SEM from five independent experiments.

a

P<0.001 vs. 2-ME

b

P<0.01 vs. CPA or IFA alone

c

P<0.01 vs. the R index of cells incubated under normoxia; one-way ANOVA and Tukey's test. The R index was calculated as described in Materials and methods. 2-ME, 2-methoxyestradiol; CPA, cyclophosphamide; IFA, ifosfamide.