nfluent cells seeded in 24 well plates. 16 hours after transfection, selleck compound cells were treated for 24 h with 9 cis retinoic acid at the indicated concentrations. Lysates from transfected cells were analyzed for luci ferase and b galactosidase activity, and data from luci ferase activity were normalized by b galactosidase activity values. Electrophoretic mobility shift assays Radiolabeled double strand oligonucleotides were mi ed with 10 ug of nuclear protein e tracts in a final volume of 20 ul of binding buffer containing 2 ug poly. After 30 minutes of incubation at room tem perature, binding comple es were separated on a 5% non denaturating polyacrylamide gel with 0. 5�� TBE buffer. The gel was vacuum dried and subjected to autoradiography. For supershift e periments, 0.

2 ug of p65 antibody was added to the samples before addition of the radiolabeled oligonucleotide. RNA interference T47D breast cancer cells were seeded 24 h prior to transfection with 100 nM siGENOME SMARTpool for cIAP2 using DharmaFECT 1 as transfection reagent according to manufacturers instructions. After 16 h, siRNA lipid comple es were removed and cells were treated with 9 cis RA for 30 h prior to etoposide treatment. Chromatin Immunoprecipitation T47D breast cancer cells growing in p150 dishes were treated with 1 uM 9 cis RA for 48 h. Media and ligands were renewed 45 min before chromatin e tracts were prepared. ChIP assays were performed according to a previously described procedure. Sonication was performed using a Bioruptor UCD 200TM from Diage node.

Chromatin comple es were incubated with primary rab bit polyclonal antibodies to acetylated H3 histone, RelA p65, RAR, R Ra, c jun or normal rabbit serum immunoglobulins. Eluted DNA from the ChIP assays were assayed directly by real time PCR. DNA inputs were diluted 1 100 previous to real time PCR assay. 1 ul of template was used per 25 ul reaction, all samples were analysed in duplicate using SYBR green 2�� PCR Master Mi on a Strata gene M 3005P real time PCR thermal cycler. After an initial denaturation and activation incubation of 10 min, 45 cycles of 2 step cycling were performed with an annealing temperature of 60 C with the following pri mers forward to amplify the cJUN promoter region containing the AP1 site. Melting curves were performed to verify product specificity.

Relative fold induction over IgG for each immunopreci pitate was assessed by analysing the change in threshold cycle number upon normalization to their respective inputs. Reverse Transcriptase Polymerase Dacomitinib Reaction Total RNA was isolated using Tri Reagent and 1 ug of RNA was used in a reverse transcription reac tion as instructed using iScript cDNA synthesis kit from Bio RAD. Statistical analysis selleck bio Students t test was performed using the Microsoft E cell software. The statistical signifi cance of difference between groups was e pressed by asterisks. Background Blood cancer cells are highly sensitive to cytostatic drugs but, depending on the cancer type, often beco