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Published on: September 1, 2019
The effect of TWIST silencing in metastatic chordoma cells
Esra Aydemir1, Ezgi Kaşikci1, Burcu Coşkunçelebi1
1Department of Genetics and Bioengineering, Faculty of Engineering, Yeditepe University , İstanbul , Turkey.
Abstract:
Chordoma is a slowly growing and invasive bone tumor with a tendency to metastasize locally in advanced stages. It is essential to discover new therapeutics that target genes involved in the metastasis of chordoma. Epithelial-mesenchymal transition (EMT) might robustly influence the metastasis of a tumor bulk. To our knowledge, this is the first time to show that EMT might have a role in chordoma metastasis. In this study, we aim to investigate the possible role of Twist, a key player transcription factor of EMT, in chordoma metastasis. The TWIST gene was silenced by short hairpins in chordoma cell line MUG-Chor1 and effects on metastasis were investigated by wound healing/gap closure and invasion assays. Twist-silenced MUG-Chor1 cells were found to be less migratory and less invasive when compared to the negative control. This study indicates that Twist might have a role in metastatic chordoma cells.
Insights
This study reveals that the Twist gene plays a role in chordoma metastasis. Silencing Twist in chordoma cells reduced their migration and invasion, suggesting it as a potential therapeutic target.
Area of Science:
- Oncology
- Cancer Metastasis Research
- Molecular Biology
Background:
- Chordoma is a slow-growing, invasive bone tumor with metastatic potential in advanced stages.
- Targeting genes involved in chordoma metastasis is crucial for developing new therapeutics.
- Epithelial-mesenchymal transition (EMT) is a known driver of tumor metastasis.
Purpose of the Study:
- To investigate the role of Twist, a key transcription factor in EMT, in chordoma metastasis.
- To determine if targeting the TWIST gene can inhibit chordoma cell metastasis.
Main Methods:
- The TWIST gene was silenced using short hairpin RNA in the MUG-Chor1 chordoma cell line.
- Wound healing/gap closure and invasion assays were performed to assess metastatic potential.
- Comparative analysis was conducted between Twist-silenced cells and a negative control group.
Main Results:
- Chordoma cells with silenced TWIST expression exhibited significantly reduced migratory capacity.
- Invasion assays demonstrated decreased invasive behavior in Twist-silenced MUG-Chor1 cells.
- These findings suggest a direct link between Twist expression and chordoma cell metastasis.
Conclusions:
- The transcription factor Twist appears to play a significant role in chordoma metastasis.
- Targeting Twist may represent a novel therapeutic strategy for managing metastatic chordoma.
- This research provides the first evidence for EMT's involvement in chordoma metastasis via the Twist pathway.
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