HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

CD63-mediated cloaking of VEGF in small extracellular vesicles contributes to anti-VEGF therapy resistance.

Abstract
Despite wide use of anti-vascular endothelial growth factor (VEGF) therapy for many solid cancers, most individuals become resistant to this therapy, leading to disease progression. Therefore, new biomarkers and strategies for blocking adaptive resistance of cancer to anti-VEGF therapy are needed. As described here, we demonstrate that cancer-derived small extracellular vesicles package increasing quantities of VEGF and other factors in response to anti-VEGF therapy. The packaging process of VEGF into small extracellular vesicles (EVs) is mediated by the tetraspanin CD63. Furthermore, small EV-VEGF (eVEGF) is not accessible to anti-VEGF antibodies and can trigger intracrine VEGF signaling in endothelial cells. eVEGF promotes angiogenesis and enhances tumor growth despite bevacizumab treatment. These data demonstrate a mechanism where VEGF is partitioned into small EVs and promotes tumor angiogenesis and progression. These findings have clinical implications for biomarkers and therapeutic strategies for ovarian cancer.
AuthorsShaolin Ma, Lingegowda S Mangala, Wen Hu, Emine Bayaktar, Akira Yokoi, Wei Hu, Sunila Pradeep, Sanghoon Lee, Paul D Piehowski, Alejandro Villar-Prados, Sherry Y Wu, Michael H McGuire, Olivia D Lara, Cristian Rodriguez-Aguayo, Christopher J LaFargue, Nicholas B Jennings, Karin D Rodland, Tao Liu, Vikas Kundra, Prahlad T Ram, Sundaram Ramakrishnan, Gabriel Lopez-Berestein, Robert L Coleman, Anil K Sood
JournalCell reports (Cell Rep) Vol. 36 Issue 7 Pg. 109549 (08 17 2021) ISSN: 2211-1247 [Electronic] United States
PMID34407412 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.
Chemical References
  • Protein Isoforms
  • Tetraspanin 30
  • Vascular Endothelial Growth Factor A
  • Bevacizumab
  • Vascular Endothelial Growth Factor Receptor-2
Topics
  • Aged
  • Animals
  • Bevacizumab (pharmacology, therapeutic use)
  • Cell Line, Tumor
  • Cell Proliferation
  • Disease Models, Animal
  • Extracellular Vesicles (metabolism, ultrastructure)
  • Female
  • Humans
  • Mice
  • Mice, Nude
  • Middle Aged
  • Neovascularization, Pathologic (metabolism, pathology)
  • Ovarian Neoplasms (drug therapy)
  • Protein Isoforms (metabolism)
  • Signal Transduction
  • Tetraspanin 30 (metabolism)
  • Vascular Endothelial Growth Factor A (antagonists & inhibitors, metabolism)
  • Vascular Endothelial Growth Factor Receptor-2 (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: