4.7 Article

Soluble syndecan-1 promotes growth of myeloma tumors in vivo

Journal

BLOOD
Volume 100, Issue 2, Pages 610-617

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood.V100.2.610

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Funding

  1. NCI NIH HHS [CA55819, CA68494] Funding Source: Medline

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Syndecan-1 (CD138) is a transmembrane heparan sulfate-bearing proteoglycan expressed by most myeloma plasma cells that regulates adhesion, migration, and growth factor activity. In patients with myeloma, shed syndecan-1 accumulates in the bone marrow, and high levels of syndecan-1 in the serum are an indicator of poor prognosis. To test the effect of soluble syndecan-1 on tumor cell growth and dissemination, ARH-77 B-lymphoid cells were engineered to produce a soluble form of syndecan-1. Controls included vector only (neo)-transfected cells and cells transfected with full-length syndecan-1 complementary DNA that codes for the cell surface form of syndecan-1. Assays reveal that all 3 transfectants have similar growth rates in vitro, but cells expressing soluble syndecan-1 are hyper-invasive in collagen gels relative to controls. When injected into the marrow of human bones that were implanted in severe combined immunodeficient mice, tumors formed by cells expressing soluble syndecan-1 grow faster than tumors formed by neo-transfected cells or by cells expressing cell surface syndecan-1. In addition, cells bearing cell surface syndecan-1 exhibit a diminished capacity to establish tumors within the mice as compared with both neo- and soluble syndecan-1-transfected cells. Tumor cell dissemination to a contralateral human bone is detected significantly more often In the tumors producing soluble syndecan-1 than In controls. Thus, high levels of soluble syndecan-1 present In patients with myeloma may contribute directly to the growth and dissemination of the malignant cells and thus to poor prognosis. (C) 2002 by The American Society of Hematology.

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