Embryonic stem cell tumor model reveals role of vascular endothelial receptor tyrosine phosphatase in regulating Tie2 pathway in tumor angiogenesis.

Abstract

Inhibiting angiogenesis has become an effective approach for treating cancer and other diseases. However, our understanding of signaling pathways in tumor angiogenesis has been limited by the embryonic lethality of many gene knockouts. To overcome this limitation, we used the plasticity of embryonic stem (ES) cells to develop a unique approach to study tumor angiogenesis. Murine ES cells can be readily manipulated genetically; in addition, ES cells implanted subcutaneously in mice develop into tumors that contain a variety of cell types (teratomas). We show that ES cells differentiate into bona fide endothelial cells within the teratoma, and that these ES-derived endothelial cells form part of the functional tumor vasculature. Using this powerful and flexible system, the Angiopoietin/Tie2 system is shown to have a key role in the regulation of tumor vessel size. Endothelial differentiation in the ES teratoma model allows gene-targeting methods to be used in the study of tumor angiogenesis.

• Authors: Zhe Li, Hui Huang, Patricia Boland, Melissa G Dominguez, Patricia Burfeind, Ka-Man Lai, Hsin-Chieh Lin, Nicholas W Gale, Christopher Daly, Wojtek Auerbach, David Valenzuela, George D Yancopoulos, Gavin Thurston
• Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 106 Issue 52 Pg. 22399-404 (Dec 29 2009) ISSN: 1091-6490 [Electronic] United States
• PMID: 20018779 (Publication Type: Journal Article)

Chemical References

• Angiopoietins
• Receptor Protein-Tyrosine Kinases
• Receptor, TIE-2
• Tek protein, mouse
• Vascular Endothelial Growth Factor Receptor-2
• Receptor-Like Protein Tyrosine Phosphatases, Class 3

Topics

• Angiopoietins (antagonists & inhibitors)
• Animals
• Cell Differentiation
• Cell Line
• Disease Models, Animal
• Embryonic Stem Cells (enzymology, pathology)
• Endothelial Cells (enzymology, pathology)
• Mice
• Mice, SCID
• Neoplasms, Experimental (blood supply, enzymology, etiology)
• Neovascularization, Pathologic
• Receptor Protein-Tyrosine Kinases (physiology)
• Receptor, TIE-2
• Receptor-Like Protein Tyrosine Phosphatases, Class 3 (deficiency, genetics, physiology)
• Teratoma (blood supply, enzymology, etiology)
• Vascular Endothelial Growth Factor Receptor-2 (physiology)