CF3-Enigmol and CF2-Enigmol in mouse xenograft
models of prostate cancer. Nude mice (n = 10–11
per group) with palpable tumors derived from PC-3 human prostate cancer
cells were treated once daily via oral gavage with either vehicle
(95:5 olive oil/EtOH), Enigmol (3 or 10 mg/kg), or CF3-Enigmol
(3 or 10 mg/kg) in the first study (a–c), or with either vehicle
(95:5 PEG400/Tween80), Enigmol (10 mg/kg), or CF2-Enigmol
(10 or 30 mg/kg) in the second study (d–f). Tumor volume and
change in body weight were measured periodically. At the end of each
study, tumors were harvested, and accumulation was measured using
LC-MS/MS. Data represent the mean ± SEM. Statistical significance
(*p < 0.05, **p < 0.01, or
***p < 0.001) of tumor growth inhibition was assessed
via a linear mixed model for repeated measurement with the autoregressive
covariance structure using Statistical Analysis System (SAS) software.
Significance of change in body mass was determined using One-Way ANOVA
followed by Sidak’s multiple comparison test.