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Oncogene ; 26(8): 1222-30, 2007 Feb 22.
Article in English | MEDLINE | ID: mdl-16924233

ABSTRACT

Although dysregulation of tight junction (TJ) proteins is observed in epithelial malignancy, their participation in epithelial transformation is poorly understood. Recently we demonstrated that expression of oncogenic Raf 1 in Pa4 epithelial cells disrupts TJs and induces an oncogenic phenotype by downregulating expression of the TJ protein, occludin. Here we report the mechanism by which Raf 1 regulates occludin expression. Raf 1 inhibited occludin transcription by repressing a minimal segment of the occludin promoter in concert with upregulation of the transcriptional repressor, Slug without influencing the well-documented transcriptional repressor, Snail. Overexpression of Slug in Pa4 cells recapitulated the effect of Raf 1 on occludin expression, and depletion of Slug by small interfering RNA abrogated the effect of Raf 1 on occludin. Finally, chromatin immunoprecipitation assays and site-directed mutagenesis demonstrated a direct interaction between Slug and an E-box within the minimal Raf 1-responsive segment of the occludin promoter. These findings support a role of Slug in mediating Raf 1-induced transcriptional repression of occludin and subsequent epithelial to mesenchymal transition.


Subject(s)
Membrane Proteins/genetics , Proto-Oncogene Proteins c-raf/metabolism , Repressor Proteins/metabolism , Tight Junctions/metabolism , Transcription Factors/metabolism , Animals , Chromatin Immunoprecipitation , Down-Regulation , E-Box Elements , Enzyme Inhibitors/pharmacology , Gene Expression Regulation , Humans , MAP Kinase Signaling System/drug effects , Membrane Proteins/analysis , Membrane Proteins/metabolism , Occludin , Rats , Snail Family Transcription Factors , Tight Junctions/chemistry , Zinc Fingers
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