s at a density of 0.36104 cells/well and 0.56104 cells/well, respectively, and transfected with IGF-1R at a final concentration of 30 nM of subtype “B”and 50 nM of subtype “A”for 48 h along with scrambled controls. After 48 h of transfection, cell viability was measured using the MTS assay. The absorbance was read at 490 nm in order to calculate the percentage viable cells. harvested 48 h and 72 h post-transfection and then stained with Annexin V-FITC and propidium iodide according to the manufacturer’s instructions. The percentage of cell death or apoptosis was quantified using a flow cytometer . Western Blotting Analysis PANC-1 and HPAC cells were transfected with IGF-1R siRNA for 48 h. After the incubation, protein was extracted from transfected cells by lysing the cell membrane using mammalian Protein Extraction Reagent according to the manufacturer’s protocol. The protein concentration was quantitated using BSA standard methodology. Equal amounts of protein were loaded and separated by SDS-polyacrylamide gels, and transferred onto PVDF membranes. The membranes were blocked with 5% BSA in 1 X TBST for 1 h and probed with a panel of primary antibodies against pAKT, AKT, Bcl-2, pERK, ERK, STAT3, IGF-1R, Notch 2, Snail, E-cadherin, N-cadherin, Zeb, Vimentin, Slug, Bax, Caspase3, PARP, pPI3K p85, PI3K p85, IR-b, pIRS-1, IRS-1, pSTAT3, COX-2, pPTEN, pmTOR, mTOR, pp70s6kinase, p70s6kinase, Caspase8 or b-actin. After washing with TBST, the membrane was incubated with secondary horseradish peroxidase-coupled antibodies and then positive bands were visualized using enhanced chemiluminescence. Clonogenicity/Colony Formation Assay in Soft Agar Colony formation assay was performed in order to measure the in vitro survival ability of a single cell to grow into a colony in an anchorageindependent growth environment. Briefly, after transfecting PANC-1 and HPAC cells with IGF-1R siRNA or scrambled control for 48 h, these transfected cells were seeded in complete media at a density of 26104 cells in 60-mm dishes containing a top layer of 0.7% agar and 
a bottom layer of 1% agar. The plates were incubated at 37uC for 3 to 4 weeks and then stained with 0.2% Crystal violet. Colonies of greater than 20 cells were counted manually. Wound Healing Assay Cell migrating ability of IGF-1R silenced pancreatic cancer cells were measured using the scratch assay. Briefly, cells were seeded in Amezinium metilsulfate web 6-well plates at a density of 3.56105 cells/well for IGF-1R transfection. At this density, PANC-1 and HPAC cells reached monolayer confluency after 486h. A straight wound or scratch was then gently created in the cell monolayers with a sterile pipette tip. Cells detached by the scratch were washed twice with PBS and cultures were then supplemented with fresh medium and monitored for 96 h at 37uC using the Biostation CT for continuous observation. The Biostation was automatically programmed to capture photographs at 2 h intervals up to 96 h. Migration images were captured and PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19655565 documented at different time points using NISElement AR software. Statistical Analysis The differences between groups were analyzed by unpaired student’s t-test. The GraphPad Prism 5 software package version 5.03 was used to do all the statistical calculations. Probability values,0.05 were considered to be statistically significant. Results IGF-1R is Highly Expressed in Pancreatic Cancers We examined the expression levels of IGF-1R in pancreatic ductal adenocarcinoma cell lines using western blot. All thr