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Updated: Aug 15, 2026

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Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis
Published on: May 1, 2015
Plasmablastic multiple myeloma is associated with increased vascular endothelial growth factor immunoexpression
C Ribas1, G W B Colleoni, M S S Almeida
1Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Summary
Plasmablastic multiple myeloma (MM) is linked to higher vascular endothelial growth factor (VEGF) levels, suggesting it drives poor prognosis. Anti-angiogenic therapies may benefit these patients.
Area of Science:
- Hematology
- Oncology
- Cancer Biology
Background:
- The negative prognostic implications of plasmablastic myeloma (MM) are not fully elucidated.
- Investigating the association between aggressive MM subtypes and the bone marrow microenvironment is crucial.
Purpose of the Study:
- To determine if histologically aggressive multiple myeloma (MM) correlates with a more angiogenic bone marrow environment.
- To explore the role of vascular endothelial growth factor (VEGF) in plasmablastic MM.
Main Methods:
- Bone marrow samples from 50 newly diagnosed multiple myeloma patients were analyzed.
- Vascular endothelial growth factor (VEGF) staining intensity in plasma cells was evaluated.
- Microvessel density was assessed in relation to plasmablastic MM features.
Main Results:
- Plasmablastic MM was identified in 12% of patients.
- Plasmablastic MM significantly correlated with moderate/strong VEGF staining in plasma cells (P = 0.036).
- No association was found between plasmablastic MM and increased microvessel density.
Conclusions:
- Increased VEGF expression on plasmablasts suggests a potential mechanism for the adverse prognosis in plasmablastic MM.
- Patients with plasmablastic MM may benefit from anti-angiogenic therapies targeting VEGF.
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