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Published on: August 29, 2018
Transgelin promotes migration and invasion of cancer stem cells
Eun-Kyung Lee1, Gi-Yeon Han, Hye Won Park
1School of Life Sciences and Biotechnology, Korea University, Seoul, Korea.
Abstract:
Recent studies have suggested the existence of a small subset of cancer cells called cancer stem cells (CSCs), which possess the ability to initiate malignancies, promote tumor formation, drive metastasis, and evade conventional chemotherapies. Elucidation of the specific signaling pathway and mechanism underlying the action of CSCs might improve the efficacy of cancer treatments. In this study, we analyzed differentially expressed proteins between tumerigenic and nontumorigenic cells isolated from the human hepatocellular carcinoma (HCC) cell line, Huh7, via proteomic analysis to identify proteins correlated with specific features of CSCs. The expression level of Transgelin was 25-fold higher in tumorigenic cells than nontumorigenic cells. Similar results were also observed in tumorigenic cells derived from colorectal adenocarcinoma and prostate carcinoma. More importantly, the elevated levels of Transgelin significantly increased the invasiveness of tumorigenic cells, whereas reduced levels decreased the invasive potential. Moreover, in tumors derived from Huh7-induced xenografts, Transgelin was also co-expressed with CXCR4, which is responsible for tumor invasion. Taken together, these results indicate that the metastatic potential of CSCs arises from highly expressed Transgelin.
Insights
Cancer stem cells (CSCs) drive metastasis. This study found that high Transgelin expression in CSCs significantly increases tumor invasiveness and metastatic potential, suggesting it as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Cancer stem cells (CSCs) are implicated in tumor initiation, metastasis, and therapy resistance.
- Understanding CSC mechanisms is crucial for improving cancer treatment efficacy.
Purpose of the Study:
- To identify proteins associated with CSC features using proteomic analysis.
- To investigate the role of differentially expressed proteins in cancer cell invasiveness.
Main Methods:
- Proteomic analysis of tumorigenic and nontumorigenic cells from hepatocellular carcinoma (HCC) cell line Huh7.
- Validation of protein expression in colorectal and prostate cancer cells.
- Assessment of Transgelin's impact on cell invasiveness in vitro and in vivo.
Main Results:
- Transgelin expression was 25-fold higher in tumorigenic cells compared to nontumorigenic cells.
- Elevated Transgelin levels significantly increased cancer cell invasiveness; reduced levels decreased it.
- Transgelin co-expressed with CXCR4 in xenograft tumors, indicating a role in tumor invasion.
Conclusions:
- High Transgelin expression is strongly correlated with the metastatic potential of cancer stem cells.
- Transgelin represents a potential therapeutic target for inhibiting CSC metastasis.
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