Review Article
PP2A-Mediated Anticancer Therapy
Table 4
PP2A-activating drugs/protein.
| Activating drugs/Proteins | Mechanism | Malignancies | Consequences | References |
| Ceramide | Activation of PP2A, leading to activation of GSK-3 or accumulation of p27 | Prostate cancer | Apoptosis; Cell cycle arrest | [48, 49] | FTY720 | Disrupt SET–PP2A interaction | Leukemia | Apoptosis | [51, 52] | Forskolin | Induces PP2A activity by increasing intracellular cAMP levels | Leukemia | Block proliferation; induce apoptosis | [62, 63] | Chloroethylnitrosourea | Augment methylation of PP2A, leading to Akt dephosphorylation | Melanoma | Reduce cell proliferation and survival | [64, 65] | Vitamin E analogues (i.e., -tocopheryl succinate) | Reduce PKC isotype (colon cancer) or inactivation of JNKs (prostate cancer) activity by increasing PP2A activity | Colon, prostate cancer | Apoptosis | [66, 67] | Carnosic acid | Downregulate AKT/IKK/NFκB by activation of PP2A | Prostate cancer | Apoptosis | [68] | Methylprednisolone | Upregulate PP2A B subunits | Myeloid leukemia | Cell differentiation | [69] | Dithiolethione
| Increase PP2A concentration | Lung, breast cancer | Inhibit proliferation | [70] | E1A | Upregulate PP2A C subunits | Breast cancer | Apoptosis | [53] |
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