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MEKK3 is required for endothelium function but is not essential for tumor growth and angiogenesis.

Abstract
Mitogen-activated protein kinase kinase kinase 3 (MEKK3) plays an essential role in embryonic angiogenesis, but its role in tumor growth and angiogenesis is unknown. In this study, we further investigated the role of MEKK3 in embryonic angiogenesis, tumor angiogenesis, and angiogenic factor production. We found that endothelial cells from Mekk3-deficient embryos showed defects in cell proliferation, apoptosis, and interactions with myocardium in the heart. We also found that MEKK3 is required for angiopoietin-1 (Ang1)-induced p38 and ERK5 activation. To study the role of MEKK3 in tumor growth and angiogenesis, we established both wild-type and Mekk3-deficient tumor-like embryonic stem cell lines and transplanted them subcutaneously into nude mice to assess their ability to grow and induce tumor angiogenesis. Mekk3-deficient tumors developed and grew similarly as control Mekk3 wild-type tumors and were also capable of inducing tumor angiogenesis. In addition, we found no differences in the production of VEGF in Mekk3-deficient tumors or embryos. Taken together, our results suggest that MEKK3 plays a critical role in Ang1/Tie2 signaling to control endothelial cell proliferation and survival and is required for endothelial cells to interact with the myocardium during early embryonic development. However, MEKK3 is not essential for tumor growth and angiogenesis.
AuthorsYong Deng, Jianhua Yang, Marya McCarty, Bing Su
JournalAmerican journal of physiology. Cell physiology (Am J Physiol Cell Physiol) Vol. 293 Issue 4 Pg. C1404-11 (Oct 2007) ISSN: 0363-6143 [Print] United States
PMID17687003 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Angiopoietin-1
  • Angpt1 protein, mouse
  • Vascular Endothelial Growth Factor A
  • Receptor, TIE-2
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase Kinase 3
  • Map3k3 protein, mouse
Topics
  • Angiopoietin-1 (pharmacology)
  • Animals
  • Aorta (metabolism, pathology)
  • Apoptosis (genetics, physiology)
  • Cell Proliferation
  • Embryo, Mammalian (metabolism, pathology)
  • Endocardium (metabolism, pathology)
  • Endothelial Cells (drug effects, metabolism, pathology)
  • Endothelium, Vascular (physiology)
  • Female
  • MAP Kinase Kinase Kinase 3 (deficiency, genetics, physiology)
  • Mice
  • Mice, Inbred Strains
  • Mice, Knockout
  • Mice, Nude
  • Mitogen-Activated Protein Kinases (metabolism)
  • Myocardium (metabolism, pathology)
  • Neoplasms, Experimental (blood supply, metabolism, pathology)
  • Neoplastic Stem Cells (metabolism, pathology)
  • Neovascularization, Pathologic (genetics, metabolism, pathology)
  • Phosphorylation (drug effects)
  • Receptor, TIE-2 (metabolism)
  • Vascular Endothelial Growth Factor A (metabolism)

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