Table 1.

Induction of DNA Fragmentation in Lympho-Hematopoietic Tumor Lines by Various Apoptosis Inducers

Reagent Dose DNA Degradation*
HL-60 U937 Jurkat K562 NALM-6Ramos Daudi Raji
DNR  1 μg/mL  +  +  − −  ND  −  −  −  
VP-16  10 μg/mL  +  +  −  ND  +  +  −  
TNF-α  20 ng/mL +  +  ND  ND  ND  ND  ND  −  
C2-ceramide 20 μmol/L  +  +  +  +  +  +  +  − 
Diamide  1 mmol/L  +  +  +  +  +  +  −  
t-BHP  50 μmol/L  +  +  +  +  +  +  −  
Anti-Fas 1 μg/mL  ND  ND  +  ND ND  −  −  −  
Irradiation 5,000 rad  +  +  ND  ND  +  +  − 
Reagent Dose DNA Degradation*
HL-60 U937 Jurkat K562 NALM-6Ramos Daudi Raji
DNR  1 μg/mL  +  +  − −  ND  −  −  −  
VP-16  10 μg/mL  +  +  −  ND  +  +  −  
TNF-α  20 ng/mL +  +  ND  ND  ND  ND  ND  −  
C2-ceramide 20 μmol/L  +  +  +  +  +  +  +  − 
Diamide  1 mmol/L  +  +  +  +  +  +  −  
t-BHP  50 μmol/L  +  +  +  +  +  +  −  
Anti-Fas 1 μg/mL  ND  ND  +  ND ND  −  −  −  
Irradiation 5,000 rad  +  +  ND  ND  +  +  − 

Abbreviation: ND, not determined.

*

Cells were cultured in 2% FCS/RPMI1640 in the presence of varying reagents for 18 hours at 37°C. DNA degradation was determined by the presence of a hypodiploid peak in cell-cycle analysis.

Cells were incubated with apoptogenic anti-Fas MoAb (IgM, clone CH-11) for 18 hours at 37°C.

Cells were irradiated with an x-ray source.

Close Modal

or Create an Account

Close Modal
Close Modal