4.8 Article

Interleukin-6 Stimulates Defective Angiogenesis

Journal

CANCER RESEARCH
Volume 75, Issue 15, Pages 3098-3107

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-15-1227

Keywords

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Categories

Funding

  1. Arthritis Research UK Grant [19207]
  2. Cancer Research UK Programme Grant [C587/A16354]
  3. European Research Council Advanced Grant [322566]
  4. MRC [G0901609, G0501974] Funding Source: UKRI
  5. Cancer Research UK [16354, 18673, 12007] Funding Source: researchfish
  6. Medical Research Council [G0501974, G0901609, 1365527] Funding Source: researchfish
  7. Versus Arthritis [19207] Funding Source: researchfish
  8. Worldwide Cancer Research [12-1068] Funding Source: researchfish
  9. Fight for Sight [1558/59] Funding Source: researchfish

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The cytokine IL6 has a number of tumor-promoting activities in human and experimental cancers, but its potential as an angiogenic agent has not been fully investigated. Here, we show that IL6 can directly induce vessel sprouting in the ex vivo aortic ring model, as well as endothelial cell proliferation and migration, with similar potency to VEGF. However, IL6-stimulated aortic ring vessel sprouts had defective pericyte coverage compared with VEGF-stimulated vessels. The mechanism of IL6 action on pericytes involved stimulation of the Notch ligand Jagged1 as well as angiopoietin2 (Ang2). When peritoneal xenografts of ovarian cancer were treated with an anti-IL6 antibody, pericyte coverage of vessels was restored. In addition, in human ovarian cancer biopsies, there was an association between levels of IL6 mRNA, Jagged1, and Ang2. Our findings have implications for the use of cancer therapies that target VEGF or IL6 and for understanding abnormal angiogenesis in cancers, chronic inflammatory disease, and stroke. (C) 2015 AACR.

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