Purpose
The interaction of p53, with its negative regulators Mdm2/4 has been widely studied [1]. In p53+/+ cells, expression of Mdm2/4 leads to p53 turnover, inhibition of downstream transcription, decreasing cell cycle arrest or apoptosis. We report in vitro cytotoxicity and in vivo efficacy, pharmacokinetics, and metabolism of YH264, YH263 and WW751, three proposed small molecule inhibitors of the Mdm2/4-p53 interaction.
Methods
MTT cytotoxicity assays were performed and alterations in proteins were examined using Western blots. Mice were dosed 150 mg/kg YH264 or YH263 iv or po QDx5. Mice were iv dosed 88 mg/kg, 57 mg/kg, or 39 mg/kg WW751 for three, five, or five days. YH264, YH263 and WW751 and metabolites were quantitated by LC-MS/MS.
Results
IC50 values for YH264, YH263 and WW751 against p53 wild type HCT 116 cells after 72 h of incubation were 18.3 ± 2.3 μM, 8.9 ± 0.6 μM, and 3.1 ± 0.2 μM respectively. Only YH264 appeared to affect p53 expression in vitro. None of the compounds affected the growth of HCT 116 xenografts in C.B-17 SCID mice. YH264 plasma half-life was 147 min; YH263 plasma half-life was 263 min; and WW751 plasma half-life was less than 120 min.
Conclusions
Despite dosing the mice at the maximum soluble doses, we could not achieve tumor concentrations equivalent to the intracellular concentrations required to inhibit cell growth in vitro. YH263 and WW751 do not appear to affect p53/Mdm2 and none of the three were active in a subcutaneous HCT116 p53+/+ xenograft model.