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2 protocols using azd5582

1

Investigating IAP Inhibitor AZD5582 Effects

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The novel IAP inhibitor AZD5582 was provided by AstraZeneca (London, UK). Fludarabine and dexamethasone were obtained from Sigma-Aldrich (Gillingham, UK). Soluble recombinant human TRAIL was purchased from Enzo Life Sciences (Exeter, UK). Mouse monoclonal antibodies against XIAP (clone 48/hILP/XIAP) and cIAP-2 (clone F30-2285,) were obtained from BD Biosciences (Oxford, UK). Goat antibody to cIAP-1 was from R&D Systems (Minneapolis, MN). Rabbit antibodies against cFLIP, Bcl-2 and Bcl-xL were from Cell Signalling Technology (New England Biolabs, Herts, UK). Rabbit antibody to Mcl-1 was from Santa Cruz Biotechnology (Insight Biotechnology, Middlesex, UK). Mouse monoclonal antibody to β-actin (clone AC-74) was from Sigma-Aldrich. Other chemicals, unless otherwise stated, were also obtained from Sigma-Aldrich.
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2

Evaluating Pancreatic Cancer Cell Lines

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Synthetic IAP antagonist, AZD5582 was supplied by AstraZeneca. Co., Ltd. (Maccelsfiled, Cheshire, UK). The human pancreatic cancer cell lines including BxPC-3, Miapaca-2, Panc-1, Panc0813, PL45, Capan-1, Capan-2 and AsPC-1 were purchased from ATCC (American Type Culture Collection, Manassas, VA, USA). All cells were cultured according to the ATCC's recommended guide lines. XIAP and cIAP1 null mouse embryonic fibroblast cells were kindly provided by Dr. Colin S. Duckett (University of Michigan, Ann Arbor, MI, USA) and Dr. Robert Korneluk (Ontario Cancer Institute, USA), respectively. Cycloheximide, a protein synthesis inhibitor, MG132, a proteasome inhibitor and z-VAD, a pan-caspase inhibitor, were provided by Sigma (St. Louis, MO, USA).
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