Bevacizumab attenuates major signaling cascades and eIF4E translation initiation factor in multiple myeloma cells

Oshrat Attar-Schneider1, Liat Drucker, Victoria Zismanov

  • 1Oncogenetic Laboratories, Meir Medical Center, Kfar Saba, Israel.

Insights

Blocking vascular endothelial growth factor (VEGF) with bevacizumab directly harms multiple myeloma (MM) cells, causing cytostasis. This inhibition affects key signaling pathways and protein translation initiation, suggesting potential for combination therapies.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cell Biology

Background:

  • Multiple myeloma (MM) is a fatal plasma cell malignancy.
  • Tumor microenvironment factors, like vascular endothelial growth factor (VEGF), contribute to MM progression.
  • Novel therapies are needed to overcome resistance and improve MM patient outcomes.

Purpose of the Study:

  • To investigate the direct anti-cancer effects of anti-VEGF treatment (bevacizumab) on multiple myeloma cells.
  • To determine the impact of VEGF inhibition on protein translation initiation in MM.
  • To explore the downstream signaling pathways affected by bevacizumab in MM.

Main Methods:

  • Experiments utilized MM cell lines and primary bone marrow (BM) samples.
  • VEGF inhibition was achieved using the anti-VEGF antibody, bevacizumab.
  • Assessed MM cell viability, proliferation, survival, and key signaling pathways including eIF4E.

Main Results:

  • Bevacizumab treatment demonstrated a direct cytostatic effect on MM cell lines and primary BM samples.
  • Inhibition of VEGF by bevacizumab attenuated critical signaling pathways: VEGFR1, mTOR, c-Myc, Akt, STAT3, and eIF4E.
  • The effect of bevacizumab on MM cell viability and eIF4E was dependent on Akt signaling.

Conclusions:

  • Bevacizumab directly impacts key MM pathways, independent of its anti-angiogenic effects.
  • VEGF inhibition shows potential as a therapeutic strategy for multiple myeloma, particularly in combination therapies.
  • Targeting protein translation initiation via VEGF inhibition may offer a novel approach for MM treatment.

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