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The transcriptional repressor SNAIL is overexpressed in human colon cancer
Hemant K Roy1, Thomas C Smyrk, Jennifer Koetsier
1Department of Internal Medicine, Evanston-Northwestern Healthcare, Evanston, Illinois 60201, USA. h-roy@northwestern.edu
Abstract:
Overexpression of the transcriptional repressor, SNAIL, has been implicated in the pathogenesis of a number of malignancies; however, there are no previous reports on the role of SNAIL in colorectal cancers (CRCs). We, therefore, evaluated human CRC specimens for the presence of the SNAIL protein. Immunohistochemical studies were performed using samples obtained from archived CRC paraffin blocks and a tissue array. Tissue sections were probed with a polyclonal antibody to human SNAIL and scored by a gastrointestinal pathologist. SNAIL was not detectable in uninvolved mucosa, but immunoreactivity was evident in 78% of tumors. SNAIL protein expression did not correlate with subsite location or gender, however, SNAIL-positive tumors had an older mean age (58.9 +/- 12.7 versus 49.8 +/- 127; P = 0.028). Furthermore, there was a trend that CRCs with metastatic ability more frequently overexpressed SNAIL (100 versus 65%; P = 0.11). In conclusion, we demonstrate, for the first time, that SNAIL is upregulated in human colon cancer, which potentially may have significance in control of metastasis and possibly serve as a target for chemopreventive agents.
Insights
SNAIL protein is overexpressed in 78% of colorectal cancers (CRCs), unlike normal tissue. This finding suggests SNAIL may play a role in CRC metastasis and could be a target for future cancer prevention strategies.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- The transcriptional repressor SNAIL is linked to various cancers.
- Its role in colorectal cancer (CRC) pathogenesis remained uninvestigated.
- Understanding SNAIL's function in CRC is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the expression and potential role of SNAIL protein in human colorectal cancer specimens.
- To determine if SNAIL expression correlates with clinical features of CRC.
Main Methods:
- Immunohistochemical analysis of SNAIL protein expression in archived CRC paraffin blocks and tissue arrays.
- Scoring of SNAIL immunoreactivity by a gastrointestinal pathologist.
- Statistical analysis to correlate SNAIL expression with clinicopathological parameters.
Main Results:
- SNAIL protein was undetectable in normal colonic mucosa.
- SNAIL was expressed in 78% of CRC tumors.
- SNAIL-positive tumors were associated with older patient age (P=0.028).
- A trend indicated higher SNAIL expression in metastatic CRCs (P=0.11).
Conclusions:
- SNAIL is significantly upregulated in human colorectal cancer.
- SNAIL overexpression may be involved in CRC metastasis.
- SNAIL represents a potential therapeutic target for chemoprevention in CRC.
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