Abstract
Inhibition of ERK-MAPK signaling by expression of dominant-negative MEK1 in the tumor vasculature suppresses angiogenesis and tumor growth. In an organotypic tissue culture angiogenesis assay, ERK-MAPK inhibition during the migratory phase results in loss of bipolarity, detachment, and cell death of isolated endothelial cells and retraction of sprouting tubules. These effects are the consequence of upregulated Rho-kinase signaling. Transient inhibition of Rho-kinase rescues the effects of ERK-MAPK inhibition in vitro and in vivo, promotes sprouting, and increases vessel length in tumors. We propose a regulatory role of Rho-kinase by ERK-MAPK during angiogenesis that acts through the control of actomyosin contractility. Our data delineate a mechanism by which ERK-MAPK promotes endothelial cell survival and sprouting by downregulating Rho-kinase signaling.
MeSH terms
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Actomyosin / metabolism
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Animals
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Cell Movement
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Cell Polarity
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Cell Survival
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Cells, Cultured
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Coculture Techniques
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Endothelial Cells / physiology*
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Endothelium, Vascular / pathology*
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Fibroblasts / cytology
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Gene Expression Regulation, Neoplastic
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Humans
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Intracellular Signaling Peptides and Proteins
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MAP Kinase Kinase 1 / genetics
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MAP Kinase Kinase 1 / metabolism*
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Male
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Mice
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Mitogen-Activated Protein Kinases / antagonists & inhibitors
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Mitogen-Activated Protein Kinases / physiology*
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Neovascularization, Pathologic / metabolism*
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Neovascularization, Pathologic / pathology
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Protein Kinase Inhibitors / pharmacology
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Protein Serine-Threonine Kinases / antagonists & inhibitors
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Protein Serine-Threonine Kinases / physiology*
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Signal Transduction
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Umbilical Veins / cytology
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rho-Associated Kinases
Substances
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Intracellular Signaling Peptides and Proteins
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Protein Kinase Inhibitors
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Actomyosin
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Protein Serine-Threonine Kinases
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rho-Associated Kinases
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Mitogen-Activated Protein Kinases
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MAP Kinase Kinase 1
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MAP2K1 protein, human