tivated in an RPMI 1640 culture www.selleckchem.com/products/INCB18424.html medium with the addition of 10% fetal bovine serum, a 1% solution of L glutamine 100X, and antibiotics, which will be desig nated as RPMI S. The cells were maintained at 37 C in a humid atmosphere containing 5% CO2 and 95% air. Drugs PTX was dissolved in a sterile saline solution at a 200 mM concen tration and stored at ?4 C during a maximum period of 1 week. The MG132 proteasome inhibitor 0. 5 mg was dissolved in 0. 250 mL of Dimethyl sulfoxide, divided into 20 uL aliquots, and stored at ?20 C. Immedi ately prior to use, this was diluted in RPMI 1640 culture medium at a final concentration of 1 uM. Cell culture and experimental conditions U937 cells were grown in RPMI S for 24 hours and collected by centrifugation.

The cells were reseeded onto 24 well plates, U937 cells were either treated with PTX or MG132, or PTX MG132. The cells were incubated with PTX for 1 hour prior to the addition of MG132. All experiments were carried out 24 hours after treat ment, to exception of the p65 phosphorylation that it was analyzed 1 hour after treatment with PTX or MG132 and in the gene expression studies the cells were incubated with the drugs for only 3 hours. The concentrations of the treatments employed in this study were previously confirmed as being the most favorable for the induction of apoptosis in this experimental model. Cellular viability Cell viability was determined at different times in U937 cells. They were incubated with PTX, MG132 or PTX MG132 during 18, 24, 36 and 48 hours, we use a WST 1 cell proliferation reagent commercial kit following the manu facturers instructions.

This study is based on the reduc tion of tetrazolium salts to formazan. After of the incubation 10 uL well of WST 1 ECS reagent was added and the U937 cell were incubated for another 3 hours. The absorbance was measured in a microplate reader at 450 nm as reading refer ence wavelength at 690 nm. Data are reported as the mean standard deviation of the optical density values obtained in each group. Cell cycle analysis by flow cytometry For cell cycle analysis, the U937 cells were synchronized.In brief, cells were culture in RPMI 1640 containing 5% FBS by 12 hours then the cells were washed and culture in RPMI 1640 containing 1% FBS overnight.

After the cells were washed with PBS and changed to serum free medium for 18 hours, and finally the cells were passage and released into cell cycle by addition of 10% FBS in RPMI 1640 culture medium and 1 �� 106 cells were treated 24 hours with the different drugs. The BD Cycletest Plus DNA Reagent Kit was used following the manufacturers instructions. DNA Dacomitinib QC Particles were used for verification of instrument performance and quality control of BD FACSAria I cell clearly sorter employed in DNA analysis. For each sample, at least 20,000 events were acquired and data were processed with Flowjo v7. 6. 5 software. Assessment of apoptosis induction by PTX and MG132 proteasome inhibitor Apoptosis was evaluated by means of