Te recombinant protein was tested for the effect upon platelet aggregation using fresh human platelet rich plasma (PRP)

as described by Higuchi et al. (2007). A PACKS-4 platelet aggregation chromogenic kinetic system (Helena Laboratories, Beautmont, TX, USA) http://www.selleckchem.com/products/EX-527.html was used to platelet aggregation monitoring. Inhibition of adenosine 5′-diphosphate (ADP)-, arachidonic acid (AA)-, and collagen-induced platelet aggregation was conducted at 37 °C by adding the recombinant protein (0.5–3 μM final concentration) 3 min before the addition of the agonist (final concentrations: ADP, 10 μM; AA, 30 μg/mL and collagen, 5 μg/mL). Ten days after intraperitoneal inoculation of cells in mice, the ascitic tumor was removed and the cells separated by centrifugation at 3000×g for 3 min. After washing the cells with saline, the cellular viability was determined using Trypan blue. Samples presenting cellular viability lower than 90% were discarded.

Viable cells (2.5 × 106) were inoculated subcutaneously in mice and in the eighth day after inoculation the treatment was initiated and lasted seven days with daily subcutaneous injections ( Higuchi et al., 2007). Groups of 20 mice were treated with three different doses of purified recombinant protein (5, 10 or 20 μg per animal per day) or 20 μg of protein from fermentation medium without methanol induction. Samples were administered subcutaneously until the 7th day (7 doses) and at the 8th day the animals were sacrificed and the tumor removed and weighed. Animals from the control group received injections of 100 μL 0.9% saline. Angiogenesis was determined indirectly by the sponge implant model in selleck products mice (Santos et al., 2010). Polyurethane sponge discs (Vitafoam Ltd., London, UK), 8 mm diameter and 5 mm thick Metalloexopeptidase were used as the matrix for fibrovascular tissue growth. The sponge discs were sterilized overnight in 70% ethanol and by boiling in distilled water for 15 min before the implantation. The animals were anesthetized by intraperitoneal injection of 2.5% tribromoethanol (Sigma Chemical Co., St Louis, MO, USA) 1 mL/100 g body weight. The sponge discs were aseptically implanted into

a subcutaneous pouch. The animals with implant had been randomly divided into two groups (n = 10 each group). Treatment initiated 24 h after the implantation with subcutaneous daily injections of purified recombinant protein (10, 25 or 50 μg per animal per day). The control group received daily injections of 100 μL 0.9% saline. In the eleventh day after the beginning of treatment (ten doses), the implanted bearing mice were anesthetized by intraperitoneal injection of tribromoethanol and killed by cervical dislocation. The sponge was removed, dissected free from adherent tissue, weighed and homogenized for hemoglobin quantitation. Hemoglobin was quantified by a colorimetric method as described by Santos et al. (2010). Hundred milligrams of the sponge implant were excised carefully. Each piece was homogenized in 2.