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 . | |||||
IC50 . | R2 . | IC50 . | R2 . | IC50 . | R2 . | IC50 . | R2 . | |
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 . | |||||
IC50 . | R2 . | IC50 . | R2 . | IC50 . | R2 . | IC50 . | R2 . | |
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.).