Related Experiment Video
Updated: Aug 16, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
The transcription factor snail induces tumor cell invasion through modulation of the epithelial cell differentiation
Bram De Craene1, Barbara Gilbert, Christophe Stove
1Unit of Molecular and Cellular Oncology, Department for Molecular Biomedical Research, VIB-Ghent University, Belgium.
Abstract:
Abberant activation of the process of epithelial-mesenchymal transition in cancer cells is a late event in tumor progression. A key inducer of this transition is the transcription factor Snail, which represses E-cadherin. We report that conditional expression of the human transcriptional repressor Snail in colorectal cancer cells induces an epithelial dedifferentiation program that coincides with a drastic change in cell morphology. Snail target genes control the establishment of several junctional complexes, intermediate filament networks, and the actin cytoskeleton. Modulation of the expression of these genes is associated with loss of cell aggregation and induction of invasion. Chromatin immunoprecipitation experiments showed that repression of selected target genes is associated with increased binding of Snail to their promoters, which contain consensus Snail-binding sites. Thus, Snail constitutes a master switch that directly represses the epithelial phenotype, resulting in malignant carcinoma cells.
Insights
The transcription factor Snail drives cancer progression by repressing epithelial genes. This master switch induces a dedifferentiation program, leading to cell invasion and malignant carcinoma formation.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Epithelial-mesenchymal transition (EMT) is crucial for tumor progression.
- Snail is a key transcription factor that induces EMT by repressing E-cadherin.
Purpose of the Study:
- To investigate the role of Snail in colorectal cancer.
- To elucidate the molecular mechanisms by which Snail induces malignant phenotypes.
Main Methods:
- Conditional expression of Snail in colorectal cancer cells.
- Analysis of Snail target genes involved in cell morphology and cytoskeleton.
- Chromatin immunoprecipitation to assess Snail binding to target gene promoters.
Main Results:
- Snail expression induced epithelial dedifferentiation and altered cell morphology.
- Snail modulated genes controlling junctional complexes, intermediate filaments, and actin cytoskeleton.
- Snail directly repressed epithelial genes, promoting cell aggregation loss and invasion.
Conclusions:
- Snail acts as a master switch for epithelial-mesenchymal transition in cancer.
- Direct repression of epithelial genes by Snail leads to malignant carcinoma development.
Related Concept Videos
Role Of Notch Signalling In Intestinal Stem Cell Renewal
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Cancer Cell Migration through Invadopodia
Cadherins in Tissue Organization
Cell Sorting During Development
Cell sorting plays an...
Hedgehog Signaling Pathway
Notch Signaling Pathway
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not until 1985...
Role of Ephrin-Eph Signalling in Intestinal Stem Cell Renewal
