An allosteric Akt inhibitor effectively blocks Akt signaling and tumor growth with only transient effects on glucose and insulin levels in vivo

作者：Cherrin Craig; Haskell Kathleen; Howell Bonnie; Jones Raymond; Leander Karen; Robinson Ronald; Watkins Aubrey; Bilodeau Mark; Hoffman Jacob; Sanderson Philip; Hartman George; Mahan Elizabeth; Prueksantanont Thomayant; Jiang Guoqiang; She Qing Bai; Rosen Neal; Sepp Lorenzino Laura; Defeo Jones Deborah; Huber Hans E^*

来源：Cancer Biology and Therapy, 2010, 9(7): 493-503.

DOI：10.4161/cbt.9.7.11100

• Akt
• inhibitor
• isozyme-specific
• pharmacodynamics
• hyperglycemia

The PI3K-Akt pathway is dysregulated in the majority of solid tumors. Pharmacological inhibition of Akt is a promising strategy for treating tumors resistant to growth factor receptor antagonists due to mutations in PI3K or PTEN We have developed allosteric, isozyme-specific inhibitors of Akt activity and activation, as well as ex vivo kinase assays to measure inhibition of individual Akt isozymes in tissues. Here we describe the relationship between PK, Akt inhibition, hyperglycemia and tumor efficacy for a selective inhibitor of Akt1 and Akt2 (AKTi). In nude mice, AKTi treatment caused transient insulin resistance and reversible, dose-dependent hyperglycemia and hyperinsulinemia. Akt1 and Akt2 phosphorylation was inhibited in mouse lung with EC50 values of 1 6 and 7 mu M, respectively, and with similar potency in other tissues and xenograft tumors. Weekly subcutaneous dosing of AKTi resulted in dose-dependent inhibition of LNCaP prostate cancer xenografts, an AR-dependent tumor with PTEN deletion and constitutively activated Akt. Complete tumor growth inhibition was achieved at 200 mpk, a dose that maintained inhibition of Akt1 and Akt2 of greater than 80 and 50%, respectively, for at least 12 h in xenograft tumor and mouse lung. Hyperglycemia could be controlled by reducing C-max, while maintaining efficacy in the LNCaP model, but not by insulin administration. AKTi treatment was well tolerated, without weight loss or gross toxicities. These studies supported the rationale for clinical development of allosteric Akt inhibitors and provide the basis for further refining of pharmacokinetic properties and dosing regimens of this class of inhibitors.

• 出版日期2010-4-1