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Blood, 1 June 2007, Vol. 109, No. 11, pp. 5002-5010. Prepublished online as a Blood First Edition Paper on February 20, 2007; DOI 10.1182/blood-2006-03-012542.
NEOPLASIA CD28-mediated regulation of multiple myeloma cell proliferation and survival1 Department of Microbiology and Immunology, University of Miami School of Medicine, FL; 2 Division of Hematology and Oncology, Department of Medicine, University of Miami School of Medicine, FL; 3 University of Miami Sylvester Comprehensive Cancer Center, FL; 4 University of South Florida College of Medicine, and H. Lee Moffitt Cancer & Research Institute, Tampa, FL; 5 Providence Hospital, Southfield, MI; 6 Department of Pathology, University of Miami School of Medicine, FL; 7 Department of Pathology and Laboratory Medicine, and Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia.
Although interactions with bone marrow stromal cells are essential for multiple myeloma (MM) cell survival, the specific molecular and cellular elements involved are largely unknown, due in large part to the complexity of the bone marrow microenvironment itself. The T-cell costimulatory receptor CD28 is also expressed on normal and malignant plasma cells, and CD28 expression in MM correlates significantly with poor prognosis and disease progression. In contrast to T cells, activation and function of CD28 in myeloma cells is largely undefined. We have found that direct activation of myeloma cell CD28 by anti-CD28 mAb alone induces activation of PI3K and NF
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