TABLE 1.
Disease | Target CK2 subunits | Combined inhibitors | Target | IC50 or Ki | Reference |
---|---|---|---|---|---|
CLL | α, α′ | Ibrutinib | BTK (Bruton’s tyrosine kinase) | 0.5 nM (Ki) | Honigberg et al. (2010) |
ALL | α, α′ | Temsirolimus | mTOR | 1.76 μM | Shor et al. (2008) |
CML | α, β | Imatinib | Bcr-Abl | 0.6 μM | Buchdunger et al. (1995) |
AML | α, β | Daunorubicin | DNA or RNA synthesis | 0.02 μM | Gewirtz (1999) |
MM | α, β | Bortezomib | 20S proteasome | 0.6 nM (Ki) | Adams et al. (1999) |