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Effects of Interferon Alpha on Myeloma Cells: Mechanisms of Differential Responsiveness

  • D. F. Jelinek
  • T. Arora
Part of the Current Topics in Microbiology and Immunology book series (CT MICROBIOLOGY, volume 224)

Abstract

Multiple myeloma is a progressive and fatal disease characterized by the accumulation of malignant plasma cells in the bone marrow. We have been interested in understanding the mechanisms of growth control in myeloma cells. By way of introduction, Figure 1 is a schematic depiction of the proposed progression from monoclonal gammopathy of undetermined significance (MGUS) into myeloma. The incidence of MGUS over the age of 60 has been shown to be approximately 1% and incidence increases to 3% in individuals over the age of 70 (reviewed in 1). Importantly, it has been shown that a significant proportion of MGUS patients will progress into myeloma over time (2). The key distinguishing features between MGUS and myeloma include the absence of lytic bone lesions (MGUS; 3) and differences in the proliferative index of the monoclonal plasma cell population. Thus, a well-documented change that occurs during the progression from MGUS to myeloma is an increase in the plasma cell labeling (proliferative index) of the plasma cell (LI; 4, 5). Because of the key differences between the growth properties displayed by benign (MGUS) and malignant (myeloma) plasma cells, we have had a keen interest in understanding the mechanisms of growth control. Figure 1 suggests that key changes that may occur during this progression include alterations in cytokine responsiveness, acquisition of autocrine growth factor expression, or alterations in cytokine receptor expression.

Keywords

Multiple Myeloma Myeloma Cell Myeloma Cell Line Plasma Cell Leukaemia Human Myeloma Cell Line 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 1997

Authors and Affiliations

  • D. F. Jelinek
    • 1
  • T. Arora
    • 1
  1. 1.Department of ImmunologyMayo Clinic FoundationRochesterUSA

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