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. 2016 Jun 20;17(6):973. doi: 10.3390/ijms17060973

Table 1.

Effect of reactive oxygen species (ROS) scavengers on gossypol and ApoG2-induced apoptosis in cancer cell lines. Cancer cell lines were incubated with different ROS scavengers, and treated with gossypol/ApoG2, as described in the Methods. Cell Death Detection ELISA Kit was used to assess the induction of apoptosis, as described above. Gossypol/ApoG2, 5 μM; TU, 700 μM thiourea; SOD, 100 μg/mL superoxide dismutase; Cat, 100 μg/mL catalase. p < 0.05 compared to treated control.

Cell Lines Treatment Apoptosis (Folds) # Effect of Scavengers (% Inhibition)
MDA-MB-231 Untreated 1.0
Gossypol 2.7
+ TU 1.65 38.89
+ SOD 1.62 40
+ Cat 1.58 41.48
ApoG2 3.4 54.41
+ TU 1.55 55.29
+ SOD 1.52 56.47
+ Cat 1.48
BxPC-3 Untreated 1.0
Gossypol 2.1
+ TU 1.14 45.71
+ SOD 1.66 20.95
+ Cat 1.49 29.05
ApoG2 2.6
+ TU 1.35 48.08
+ SOD 1.63 37.31
+ Cat 1.58 39.23
PC3 Untreated 1.0
Gossypol 2.3
+ TU 1.13 50.87
+ SOD 1.68 26.96
+ Cat 1.54 33.04
ApoG2 2.9
+ TU 1.38 52.41
+ SOD 1.78 38.62
+ Cat 1.53 47.24

# Fold-apoptosis was calculated relative to untreated control by direct comparison of O.D. values at 405 nm (O.D. value of treatment group/O.D. value of untreated control). Inhibitory effect of scavengers (% Inhibition) was determined by the formula—[(a − b)/a] × 100, where a = fold apoptosis by Gossypol/ApoG2 and b = fold apoptosis in presence of scavenger (TU/SOD/Cat).