Abstract
The migration-inducing gamma2 chain of laminin-5, one of the best known invasion markers, is strongly overexpressed in disseminating and infiltrating tumor cells at the invasive front of colorectal carcinomas. The same tumor cells show nuclear accumulation of the oncoprotein beta-catenin, which together with T-cell factor-DNA-binding proteins, functions as transcriptional activator of genes involved in tumor progression. Here we show that beta-catenin activates the human laminin-5 gamma2 gene through two T-cell factor-binding elements in a synergistic manner together with hepatocyte growth factor and conclude that laminin-5 gamma2 is another important target gene of nuclear beta-catenin during tumor progression.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenocarcinoma / genetics
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Adenocarcinoma / metabolism*
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Adenocarcinoma / pathology
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Binding Sites
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Cell Nucleus / metabolism
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Colorectal Neoplasms / genetics
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Colorectal Neoplasms / metabolism*
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Colorectal Neoplasms / pathology
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Cytoskeletal Proteins / biosynthesis
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Cytoskeletal Proteins / genetics
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Cytoskeletal Proteins / physiology*
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Gene Expression Regulation, Neoplastic
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Humans
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Laminin / biosynthesis*
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Laminin / genetics
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Neoplasm Invasiveness
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Promoter Regions, Genetic
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TCF Transcription Factors
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Trans-Activators*
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Transcription Factor 7-Like 2 Protein
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Transcription Factors / metabolism
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Transcriptional Activation
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beta Catenin
Substances
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CTNNB1 protein, human
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Cytoskeletal Proteins
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LAMC2 protein, human
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Laminin
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TCF Transcription Factors
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TCF7L2 protein, human
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Trans-Activators
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Transcription Factor 7-Like 2 Protein
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Transcription Factors
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beta Catenin