Fig. 6From: Mutant p53 murine oviductal epithelial cells induce progression of high-grade serous carcinoma and are most sensitive to simvastatin therapy in vitro and in vivoSimvastatin inhibits ovarian cancer disease progression, increases apoptosis and HMGCR cytoplasmic localization, but does not influence YAP or small GTPase expression. A Mice were subjected to daily intraperitoneal injections of simvastatin (1 mg/kg) or PBS for 25 days, then tumors were collected and weighed (n = 8–9/group). B TUNEL staining (n = 6/group) was performed on PBS and simvastatin treated tumors. C Cytoplasmic and nuclear protein fractions were collected from flash-frozen PBS and simvastatin treated tumors (n = 3/group) and western blotting was performed for HMGCR and YAP. D PBS and simvastatin treated tumors (n = 6/group) were immunohistochemically stained for the small GTPases, Rho and Rac1. Bars represent mean ± SEM (**p < 0.01, ***p < 0.001). Scale bars: 100 μm. Abbreviations: C cytoplasmic; N nuclearBack to article page