Abstract
We have previously reported that Bcl-w enhances the invasiveness of gastric cancer cells by inducing MMP-2 expression via phosphoinositide 3-kinase (PI3K), Akt and Sp1. This study demonstrates that Bcl-w additionally induces uPA expression and FAK activation. Analyses of the hierarchical relationship and functions of these components showed that the PI3K-Akt-Sp1 pathway also mediates the induction of uPA, and that both uPA and MMP-2 contribute to Bcl-w-induced invasion via the stimulation of the FAK-dependent migratory pathway. These findings significantly advance our understandings of the Bcl-w-induced signaling processes that results in the migration and invasion of cancer cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Apoptosis Regulatory Proteins / physiology*
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Cell Line, Tumor
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Cell Movement
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Focal Adhesion Protein-Tyrosine Kinases / physiology
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Humans
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Matrix Metalloproteinase 2 / physiology
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Phosphatidylinositol 3-Kinases / physiology
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Proto-Oncogene Proteins c-akt / physiology
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Signal Transduction / physiology*
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Sp1 Transcription Factor / physiology
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Stomach Neoplasms / pathology*
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Urokinase-Type Plasminogen Activator / physiology
Substances
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Apoptosis Regulatory Proteins
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BCL2L2 protein, human
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Sp1 Transcription Factor
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Phosphatidylinositol 3-Kinases
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Focal Adhesion Protein-Tyrosine Kinases
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Proto-Oncogene Proteins c-akt
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Urokinase-Type Plasminogen Activator
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Matrix Metalloproteinase 2