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Updated: Aug 6, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
Differential expression of vascular endothelial growth factors and their receptors in multiple myeloma
Teresa Kimlinger1, Michael Kline, Shaji Kumar
1Division of Hematology, Department of Internal Medicine, Mayo Clinic 200 First St SW, Rochester, MN 55905, USA.
Background And Objectives:
Bone marrow angiogenesis is increased in patients with multiple myeloma (MM) and correlates with disease stage.
Design And Methods:
Previous studies of quantifying vascular endothelial growth factor (VEGF) and VEGF receptors (VEGFR) in plasma cells from patients at different stages of MM found no significant difference in expression between overt MM and earlier pre-malignant stages of the disease namely, monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM).
Results:
In this report we used quantitative flow cytometry to study cytoplasmic VEGF (cyVEGF) expression (measured as antibody binding capacity) in plasma cells from patients with MM (n = 22), MGUS/SMM (n = 12), and AL-amyloidosis (AL) (n = 9). CyVEGF expression was higher in MM (169,591) than in MGUS/SMM (144,858), or AL (106,011) although these differences were not statistically significant. Using an indirect VEGFR assay that measures VEGF binding, we found VEGF receptors on plasma cells from all groups of patients, with the lowest expression on plasma cells from normal individuals. We detected VEGF R1, VEGF R2, and VEGF R3 on plasma cells from all groups of patients and found receptor expression predominantly in the subset of CD45-positive plasma cells.
Interpretation And Conclusions:
This study supports the concept that VEGF is involved in the pathogenesis of MM, and suggests that VEGF may differentially affect a subset of plasma cells.
Insights
Vascular Endothelial Growth Factor (VEGF) is implicated in multiple myeloma (MM) pathogenesis. This study found higher cytoplasmic VEGF in MM plasma cells, suggesting VEGF may impact specific plasma cell subsets in MM progression.
Area of Science:
- Oncology
- Molecular Biology
- Hematology
Background:
- Bone marrow angiogenesis is elevated in multiple myeloma (MM) and correlates with disease severity.
- Previous research showed no significant difference in plasma cell vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) expression between overt MM and earlier stages like monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM).
Purpose of the Study:
- To investigate cytoplasmic VEGF (cyVEGF) expression in plasma cells from patients with MM, MGUS/SMM, and AL-amyloidosis (AL).
- To quantify VEGF receptors (VEGFRs) on plasma cells across different disease stages.
Main Methods:
- Quantitative flow cytometry was employed to measure cyVEGF expression in plasma cells.
- An indirect VEGFR assay was used to assess VEGF binding capacity on plasma cells.
- Plasma cells from patients with MM (n=22), MGUS/SMM (n=12), AL (n=9), and normal individuals were analyzed.
Main Results:
- Cytoplasmic VEGF expression was numerically higher in MM plasma cells (169,591) compared to MGUS/SMM (144,858) and AL (106,011), though not statistically significant.
- VEGF receptors (VEGFR1, VEGFR2, VEGFR3) were detected on plasma cells from all patient groups, with the lowest expression in normal individuals.
- Receptor expression was primarily observed on CD45-positive plasma cells.
Conclusions:
- The findings support the role of VEGF in the pathogenesis of multiple myeloma.
- VEGF may exert differential effects on specific subsets of plasma cells, contributing to MM progression.
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