Abstract
Lipocalin 2, an iron-siderophore-binding protein, converts embryonic kidney mesenchyme to epithelia. We found that lipocalin 2 could also convert 4T1-Ras-transformed mesenchymal tumor cells to an epithelial phenotype, increase E-cadherin expression, and suppress cell invasiveness in vitro and tumor growth and lung metastases in vivo. The Ras-MAPK pathway mediated the epithelial to mesenchymal transition in part by increasing E-cadherin phosphorylation and degradation. Lipocalin 2 antagonized these effects at a point upstream of Raf activation. Lipocalin 2 action was enhanced by iron-siderophore. These data characterize lipocalin 2 as an epithelial inducer in Ras malignancy and a suppressor of metastasis.
MeSH terms
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Acute-Phase Proteins / genetics
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Acute-Phase Proteins / metabolism*
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Animals
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Cadherins / metabolism
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Cell Line
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Cell Transformation, Neoplastic
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Enzyme Activation
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Enzyme Inhibitors / metabolism
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Epithelial Cells / cytology
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Epithelial Cells / physiology
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Humans
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Iron / metabolism
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Lipocalin-2
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Lipocalins
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MAP Kinase Signaling System / physiology
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Mesoderm / cytology
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Mesoderm / physiology
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Mitogen-Activated Protein Kinases / metabolism
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Neoplasm Invasiveness*
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Neoplasms / metabolism
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Neoplasms / pathology*
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Oncogene Proteins / genetics
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Oncogene Proteins / metabolism*
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Proteasome Endopeptidase Complex / metabolism
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Proteasome Inhibitors
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Proto-Oncogene Proteins
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raf Kinases / metabolism
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ras Proteins / genetics
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ras Proteins / metabolism*
Substances
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Acute-Phase Proteins
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Cadherins
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Enzyme Inhibitors
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LCN2 protein, human
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Lipocalin-2
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Lipocalins
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Oncogene Proteins
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Proteasome Inhibitors
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Proto-Oncogene Proteins
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Iron
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raf Kinases
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Mitogen-Activated Protein Kinases
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Proteasome Endopeptidase Complex
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ras Proteins