Table 1

IC50 of proteasome inhibitors and chemotherapeutic agents

DrugHBL2 PTHBL2 BRFold increaseJEKO PTJEKO BRFold increase
Bortezomib, nM 489.7 81.62 4.9 213.8 43.63 
MG-132, μM 0.47 1.61 3.42 0.65 2.4 3.69 
NLVS, μM 15.8 7.8 2.6 16.6 6.38 
Etoposide, μM 1.25 0.60 0.48 3.8 1.9 0.50 
Fludarabine, μM 1.9 0.65 0.34 0.7 0.45 0.64 
Hydrocortisone, μM 60.25 44.67 0.74 87.09 25.12 0.29 
DrugHBL2 PTHBL2 BRFold increaseJEKO PTJEKO BRFold increase
Bortezomib, nM 489.7 81.62 4.9 213.8 43.63 
MG-132, μM 0.47 1.61 3.42 0.65 2.4 3.69 
NLVS, μM 15.8 7.8 2.6 16.6 6.38 
Etoposide, μM 1.25 0.60 0.48 3.8 1.9 0.50 
Fludarabine, μM 1.9 0.65 0.34 0.7 0.45 0.64 
Hydrocortisone, μM 60.25 44.67 0.74 87.09 25.12 0.29 

IC50 was determined in triplicate by MTT at 48 hours of drug exposure.

NLVS indicates 4-hydroxy-5-iodo-3-nitrophenylacetyl-Leu-Leu-leucinal-vinyl sulfone.

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