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. 2015 Mar 26;6(3):e1704. doi: 10.1038/cddis.2015.13

Table 1. Cell death was monitored in U251 after irradiation (5 Gy), ETO (50 μg/ml), TRAIL (50 ng/ml), FasL (60 ng/ml) or cisplatin (15 μg/ml) treatment after 5, 24, 48 and 72 h by FACS analysis using propidium iodide incorporation and caspase-3 activation.

  CTR 6 h 24 h 48 h 72 h
Etoposide
 % Dead cells 2.6±0.8 (n=3) NA 28±2 (n=4) 28±3 (n=4) NA
 DEVDase activity 3.3±0.3 (n=3) 37±11 (n=4) 204±18 (n=4) 128±11 (n=4) NA
           
Irradiation
 % Dead cells 2.6±0.8 (n=3) NA 6±2 (n=3) 8±1 (n=3) 15±1 (n=5)
 DEVDase activity 3.3±0.3 (n=3) NA 65±25 (n=3) NA 143±13 (n=5)
           
TRAIL
 % Dead cells 2.6±0.8 (n=3) 22±3 (n=4) 6.4±1 (n=3) NA NA
 DEVDase activity 3.3±0.3 (n=3) 107±3 (n=4) 7±0.3 (n=3) NA NA
           
FASL
 % Dead cells 2.6±0.8 (n=3) 10±1 (n=3) 20±3 (n=3) NA NA
 DEVDase activity 3.3±0.3 (n=3) 38±8 (n=3) 115±3 (n=3) 51±13 (n=3) NA
           
Cisplatin
 % Dead cells 2.6±0.8 (n=3) NA 16±2 (n=3) NA NA
 DEVDase activity 3.3±0.3 (n=3) NA 139±18 (n=3) NA NA

Abbreviation: NA, not applicable

Apoptosis was measured through caspase-3 activation