OVCAR-3 is a Enzalutamide in vitro highly Rho inhibitor metastatic, drug resistant human ovarian carcinoma cell line, and thus it is an ideal model to study the effects and mechanisms of various anticancer agents [20]. Besides, MDAH-2774 represents an example of slow-growing tumor type and was chosen a reciprocal experimental effect when used with OVCAR-3. Methods Cell lines and reagents

Human ovarian OVCAR-3 and MDAH-2774 cancer cells were obtained from ICLC (Genova, Italy). The cells were grown as monolayers in adherent cell lines and were routinely cultured in RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum (FBS), 1% L-glutamine, 1% penicillin-streptomycin in 75 cm2 polystyrene flasks (Corning Life Sciences, UK) and maintained at 37°C in a humidified atmosphere with 5% CO2. Cell culture supplies were obtained from Biological Industries (Kibbutz Beit Haemek, Israel). ATRA was obtained from Sigma Chemical Co (USA). Zoledronic acid was a generous gift from Novartis Pharmaceuticals Inc. (Basel, Switzerland). The stock solution of ATRA was prepared in DMSO (43 mM) and, zoledronic acid (10 mM) was prepared in distilled water. The check details DMSO concentration in the assay did not exceed 0.1% and was not cytotoxic

to the tumor cells. All other chemicals, unless mentioned, were purchased from Sigma. XTT cell viability assay After verifying cell viability using trypan blue dye exclusion test by Cellometer automatic cell counter (Nexcelom Inc., USA.), cells were seeded at approximately 1×104/well in a final volume of 200 μl in 96-well flat-bottom microtiter plates with or without various concentrations of drugs. Plates were incubated Interleukin-2 receptor at

37°C in a 5% CO2 incubator for the indicated time periods. At the end of incubation, 100 μl of XTT (2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide) (Roche Applied Science, Mannheim, Germany) was added to each well, and plates were incubated at 37°C for another 4 hours. Absorbance was measured at 450 nm against a reference wavelength at 650 nm using a microplate reader (Beckman Coulter, DTX 880 Multimode Reader). The mean of triplicate experiments for each dose was used to calculate the IC50 and the combination index (CI) values. Evaluation of apoptosis Apoptosis was evaluated by enzyme-linked immunosorbent assay (ELISA) using Cell Death Detection ELISA Plus Kit (Roche Applied Science, Mannheim, Germany) and verified by measuring caspase 3/7 enzyme activity (Caspase-Glo 3/7 Assay, Promega, Madison, WI). Assays were described in our previous study [21]. Examination of the expression levels of apoptotic genes by oligoarray method Expression levels of apoptosis specific genes were examined by Human Apoptosis OligoGEArray® (SuperArray, Frederick, MD).