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      TRAIL is a potent inducer of apoptosis in myeloma cells derived from multiple myeloma patients and is not cytotoxic to hematopoietic stem cells.

      Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K
      ADP-ribosyl Cyclase, Antigens, CD, Antigens, CD34, analysis, Antigens, CD38, Antigens, CD45, Antigens, Differentiation, Apoptosis, drug effects, Apoptosis Regulatory Proteins, Cell Division, Cells, Cultured, Colony-Forming Units Assay, Dose-Response Relationship, Drug, Flow Cytometry, Genes, bcl-2, genetics, Hematopoietic Stem Cells, cytology, metabolism, pathology, Humans, Membrane Glycoproteins, pharmacology, Methylcellulose, Multiple Myeloma, NAD+ Nucleosidase, Paclitaxel, Proto-Oncogene Proteins c-bcl-2, TNF-Related Apoptosis-Inducing Ligand, Time Factors, Transfection, Tumor Cells, Cultured, Tumor Necrosis Factor-alpha

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          Abstract

          TRAIL, the ligand for the newly discovered DR-4 and DR-5 receptor, is a member of the TNF family of death signal transduction proteins with a mechanism of cell death similar to that of Fas and Fas ligand (Fas-L) system. We provide first time evidence that TRAIL is a potent inducer of apoptosis in multiple myeloma (MM) cell lines. TRAIL effectively induced extensive apoptosis in 8226 and ARP-1 MM cells in a time- and dose-dependent manner. Apoptosis with TRAIL reached about 80% within 48 h of treatment with a dose of 160 ng/ml. Furthermore, we provide first time evidence that similar to Fas, TRAIL-induced apoptosis is not blocked by bcl-2 in MM cell lines. Most importantly, TRAIL induced substantial apoptosis in freshly isolated, flow-sorted myeloma cells obtained from different MM patients expressing variable levels of bcl-2. Finally, we demonstrate for the first time that TRAIL is not cytotoxic to purified CD34+/CD45dim hematopoietic stem cells and does not inhibit CFU-GM or BFU-E colony formation in methylcellulose.

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