The most intriguing data identified many of the methy lated targets as members of the IL 6 STAT3 signaling pathway. Further investigation demonstrated that Stat3 was increased in these invasive cells, and cells infected with an shRNA against either BM or SO 1 resulted in decreased levels of activated STAT3. However, only the differentially methylated So 1 directly interacts with STAT3. Thus, in our model SO 1 plays a critical role in regulating invasive prostate cancer cells. Inhibitors,Modulators,Libraries These aggressive sub populations of cells may be linked to the cancer stem cell hypothesis, making their patterns of epigenetic regulation very attractive for biomarker analysis. Materials and methods Cell Lines and Reagents LNCaP and DU145 human prostate cancer cell lines were obtained from ATCC and cultured Inhibitors,Modulators,Libraries accordingly.

Primary human prostate cancer cells were acquired Cilengitide from Celprogen and maintained as recommended using spe cific coated culture plates and defined media. Human bone marrow derived mesenchymal stem cells were obtained from Lonza and maintained using their recommended conditions. The cultures were maintained in 5% CO2 air at 37 C. Human serum was obtained from Gemini Bioproducts. The following inhibitors were also used Anti human IL 6 antibody, PI3K inhibitor LY294002, Tec Kinase inhibitor LFM A13, MEK inhibitor PD98059, JAK inhibitor AG490, and STAT3 inhibitor Stattic. Matrigel Invasion Assay Matrigel coated 24 well inserts and non coated control inserts purchased from BD Bios ciences were used according to manufac turers instructions. A range of 20,000 100,000 cells were seeded for the invasion.

Cells were seeded in serum free RPMI and migrated toward media specific for stem cells containing DMEM Inhibitors,Modulators,Libraries F12 with human supplementation of 10 ng mL bFGF, 20 ng mL EGF and 5 ug mL insulin along with 0. 4% BSA. Routine invasion assays were performed for 24 hours and then stained with the Diffi Quick Staining kit. Three to five microscopic fields were photographed and counted for each sample. Percent invasion was calculated as average number of cells field Inhibitors,Modulators,Libraries divided by average number of cells field. Values were averaged from 2 5 inde pendent e periments. For the isolation of cells from top non invading and bottom invading cells, parallel inva sion chambers were setup. For non invading cells, the bottom of the membrane was scrubbed with a cotton swab and cells on top were harvested using 500 uL of Accutase incubated at 37 C for 5 minutes. To obtain the invading cells, the top of the membrane was scrubbed with a cotton swab and the chambers were placed into another 24 well plate con taining 500 uL of Accutase incubated at 37 C for 5 minutes. MeDIP Arrays Matrigel invasion assays were carried out as previously described.