Table 1

Mutant JAK3s are sensitive to JAK3, PI3K, and mTOR inhibitors

Tofacitinib, μM
BEZ-235, nM
BKM-120, μM
CI-1040, nM
JAK3
PI3K/mTOR
PI3K
ERK 1/2
IC50R2IC50R2IC50R2IC50R2
BaF3 ND 0.77 ND 0.60 ND 0.55 ND 0.88 
WT 0.18 0.84 ND 0.44 ND 0.65 ND 0.72 
A572V 0.22 0.99 12.55 0.86 3.12 0.92 ND 0.73 
L156P 0.27 0.99 11.96 0.90 2.51 0.93 ND 0.64 
E183G 0.09 0.99 18.14 0.96 1.99 0.91 ND 0.62 
R172Q 0.08 0.90 19.21 0.84 9.12 0.96 ND 0.50 
Tofacitinib, μM
BEZ-235, nM
BKM-120, μM
CI-1040, nM
JAK3
PI3K/mTOR
PI3K
ERK 1/2
IC50R2IC50R2IC50R2IC50R2
BaF3 ND 0.77 ND 0.60 ND 0.55 ND 0.88 
WT 0.18 0.84 ND 0.44 ND 0.65 ND 0.72 
A572V 0.22 0.99 12.55 0.86 3.12 0.92 ND 0.73 
L156P 0.27 0.99 11.96 0.90 2.51 0.93 ND 0.64 
E183G 0.09 0.99 18.14 0.96 1.99 0.91 ND 0.62 
R172Q 0.08 0.90 19.21 0.84 9.12 0.96 ND 0.50 

mTOR indicates mammalian target of rapamycin; WT, wild type; and ND, IC50 not determined due to poor curve-fitting models.

Live cells were quantified by the MTT assay after 24 hours on inhibitor. IC50 and goodness-of-fit (R2) values for each mutant transduced into BaF3 cells were calculated based on best fit curves (see supplemental Figures 4,Figure 5–6 for individual curves.).

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