TABLE 5

Analysis of expression of TRAIL receptors in A549 and A549/Pt cells after exposure to ATO and sanguinarine

Drug-induced expression levels of TRAIL-R1 (DR4) and TRAIL-R2 (DR5) were determined by cytofluorometric analysis after 24-hour exposure to arsenic trioxide (10 and 30 μM in A549 and A549/Pt cells, respectively), sanguinarine (1 and 2 μM in A549 and A549/Pt cells, respectively), or to the combined treatment. Results on modulation of TRAIL receptor expression are expressed as the mean fluorescence intensity (MFI). MFI values (± S.D.) from three experiments are reported. Control refers to cells incubated with isotypic control.

MFI
ControlTRAIL-R1TRAIL-R2
A549
 Untreated4.15 ± 0.9155.8 ± 5.5168.60 ± 8.2
 ATO5.14 ± 0.9146.9 ± 15.6156.70 ± 19.8
 S8.18 ± 0.3168.40 ± 22.9150.20 ± 5.2
 S+ATO7.04 ± 1.0143.80 ± 16.05645.50 ± 76.9*
A549/Pt
 Untreated2.64 ± 0.334.44 ± 2.861.74 ± 5.3
 ATO2.87 ± 0.434.77 ± 4.1206.20 ± 15.6*
 S5.3 ± 0.848.80 ± 5.162.11 ± 3.5
 S+ATO4.57 ± 0.419.14 ± 6.7174.90 ± 5.08*
  • * P < 0.05, unpaired t test of control versus treated A549 cells.