The Low Expression of IL-37 Involved in Multiple Myeloma - Associated Angiogenesis

Zun-Chang Li1, Ming-Dong Sun2, Yong-Qing Zheng2

  • 1Department of Hemotology, Provincial Hospital, Shandong University, Jinan, Shandong, China (mainland).

Insights

Serum IL-37 levels are lower in multiple myeloma (MM) patients, correlating negatively with angiogenesis factors like VEGF. IL-37 may serve as a biomarker for MM progression and angiogenesis.

Area of Science:

  • Immunology
  • Oncology
  • Biochemistry

Background:

  • Angiogenesis is crucial in inflammatory processes and multiple myeloma (MM) pathogenesis.
  • Interleukin-37 (IL-37) is a proinflammatory cytokine with antitumor potential.
  • The role of IL-37 in MM requires further clinical investigation.

Purpose of the Study:

  • To assess the clinical significance of IL-37 in patients with multiple myeloma.
  • To investigate the correlation between IL-37 levels and angiogenesis factors in MM.
  • To determine the effect of IL-37 on endothelial cell function.

Main Methods:

  • Serum IL-37, vascular endothelial growth factor (VEGF), and angiotensin-2 (Ang-2) levels were measured in 45 MM patients and 30 healthy controls.
  • Correlations between IL-37, VEGF, Ang-2, and MM staging were analyzed.
  • In vitro assays assessed the impact of recombinant human IL-37 (rhIL-37) on human umbilical vein endothelial cell (HUVEC) tube formation.

Main Results:

  • MM patients exhibited lower serum IL-37 levels compared to healthy controls.
  • VEGF and Ang-2 levels were elevated in MM patients, increasing with disease stage.
  • Serum IL-37 negatively correlated with VEGF and Ang-2; VEGF positively correlated with Ang-2.
  • rhIL-37 pretreatment suppressed HUVEC tube formation.

Conclusions:

  • Serum IL-37 levels are implicated in the pathophysiology and progression of multiple myeloma.
  • IL-37 may function as a potential biomarker for MM disease stage and associated angiogenesis.
  • Targeting IL-37 could offer therapeutic strategies for managing MM-related angiogenesis.