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Updated: Apr 30, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
MicroRNA-1 (miR-1) inhibits chordoma cell migration and invasion by targeting slug
Eiji Osaka1, Xiaoqian Yang, Jacson K Shen
1Sarcoma Biology Laboratory, Department of Orthopedic Surgery, Massachusetts General Hospital, 50 Fruit Street, Jackson 1115, Boston, Massachusetts, 02114; Department of Orthopaedic Surgery, Nihon University School of Medicine, 30-1 Oyaguchikami-cho, Itabashi-ku, Tokyo, 173-8610, Japan.
Abstract:
Recent studies have revealed that expression of miRNA-1 (miR-1) is frequently down-regulated in several cancer types including chordoma. Identifying and validating novel targets of miR-1 is useful for understanding the roles of miR-1 in chordoma. We aimed to further investigate the functions of miR-1 in chordoma. Specifically, we assessed whether restoration of miR-1 affects cell migration and invasion in chordoma, and focused on the miR-1 potential target Slug gene. Migratory and invasive activities were assessed by wound healing and Matrigel invasion assays, respectively. Cell proliferation was determined by MTT assay. Slug expression was evaluated by Western blot, immunofluorescence, and immunohistochemistry. Restoration of miR-1 expression suppressed the migratory and invasive activities of chordoma cells. Transfection of miR-1 inhibited cell proliferation both time- and dose-dependently in chordoma. MiR-1 transfected cells showed inhibited Slug expression. Slug was over-expressed in chordoma cell lines and advanced chordoma tissues. In conclusion, we have shown that miR-1 directly targets the Slug gene in chordoma. Restoration of miR-1 suppressed not only proliferation, but also migratory and invasive activities, and reduced the Slug expression in chordoma cells. These results collectively indicate that miR-1/Slug pathway is a potential therapeutic target because of its crucial roles in chordoma cell growth and migration.
Insights
MicroRNA-1 (miR-1) down-regulation in chordoma was investigated. Restoring miR-1 suppressed chordoma cell proliferation, migration, and invasion by targeting the Slug gene, indicating a potential therapeutic pathway.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- MicroRNA-1 (miR-1) expression is frequently reduced in various cancers, including chordoma.
- Understanding miR-1 targets is crucial for elucidating its role in chordoma pathogenesis.
Purpose of the Study:
- To investigate the functional role of miR-1 in chordoma.
- To determine if miR-1 restoration impacts chordoma cell behavior.
- To validate Slug as a direct target of miR-1 in chordoma.
Main Methods:
- Chordoma cell lines were transfected with miR-1 mimics.
- Cell proliferation was assessed using MTT assays.
- Cell migration and invasion were evaluated via wound healing and Matrigel assays.
- Slug gene and protein expression were analyzed using Western blot, immunofluorescence, and immunohistochemistry.
Main Results:
- Restoration of miR-1 significantly inhibited chordoma cell proliferation, migration, and invasion.
- miR-1 transfection led to a time- and dose-dependent decrease in cell proliferation.
- Slug expression was suppressed in miR-1-transfected cells.
- Slug was found to be overexpressed in chordoma cell lines and tissues.
Conclusions:
- miR-1 directly targets the Slug gene in chordoma.
- The miR-1/Slug pathway plays a critical role in chordoma cell growth, proliferation, and migration.
- The miR-1/Slug pathway represents a potential therapeutic target for chordoma treatment.
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