Bone marrow microvascular density and angiogenic growth factors in multiple myeloma

Michael G Alexandrakis1, Freda J Passam, Emmanuel Ganotakis

  • 1Department of Hematology, University Hospital of Heraklion, Crete, Greece. freda@med.uoc.gr

Insights

Angiogenesis, measured by microvascular density and levels of hepatocyte growth factor (HGF) and tumor necrosis factor-alpha (TNF-alpha), is elevated in multiple myeloma (MM) and decreases with effective treatment.

Area of Science:

  • Oncology
  • Hematology
  • Cell Biology

Background:

  • Angiogenesis is crucial in multiple myeloma (MM) progression.
  • Hepatocyte growth factor (HGF) and tumor necrosis factor-alpha (TNF-alpha) are key pro-angiogenic cytokines.

Purpose of the Study:

  • To evaluate microvascular density (MVD) and serum levels of HGF and TNF-alpha in newly diagnosed MM patients.
  • To assess changes in MVD, HGF, and TNF-alpha after chemotherapy in MM patients reaching a plateau phase.

Main Methods:

  • Bone marrow biopsies from 43 newly diagnosed MM patients were immunostained for MVD using anti-CD34 antibodies.
  • Serum levels of HGF and TNF-alpha were measured in MM patients and healthy controls.
  • Reevaluation of MVD, HGF, and TNF-alpha was performed in 24 patients after achieving a plateau phase.

Main Results:

  • Newly diagnosed MM patients exhibited elevated MVD and serum HGF/TNF-alpha compared to healthy controls.
  • Pre-treatment MVD, HGF, and TNF-alpha levels correlated positively with MM disease stage.
  • Effective chemotherapy led to significant reductions in MVD, HGF, and TNF-alpha levels.

Conclusions:

  • Angiogenesis, indicated by bone marrow MVD and serum HGF/TNF-alpha, is upregulated in MM and escalates with disease stage.
  • Therapeutic interventions effectively reduce markers of angiogenesis in multiple myeloma.

Related Concept Videos

Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...
The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
Differentiation of Common Myeloid Progenitor Cells01:15

Differentiation of Common Myeloid Progenitor Cells

Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...