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Updated: Feb 26, 2026

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
Published on: June 7, 2019
Runx3 inhibits melanoma cell migration through regulation of cell shape change
Xin Zhang1, Linghui Wang1, Xianlu Zeng1
1The Key Laboratory of Molecular Epigenetics of MOE, Institute of Genetics and Cytology, Northeast Normal University, Changchun, Jilin 130024, China.
Abstract:
The transcription factor Runx3 is a known tumor suppressor gene, and its expression is frequently lost in melanoma. However, the potential contribution of the loss of Runx3 expression to melanoma development and progression remains unclear. In this in vitro study, we demonstrated that ectopic Runx3 re-expression in B16-F10 melanoma cells changed the cell shape from elongated and branched to spread and unbranched, which enhanced stress fiber formation, increased the number of mature and fibrillar focal adhesions, and up-regulated fibronectin expression. In association with the cell shape change, the Runx3 re-expression in B16-F10 melanoma cells inhibited cell migration. Moreover, the phenotype of the Runx3 induced cell shape change was partially resembled when the melanoma cells were cultured on a fibronectin-coated coverslip, suggesting that fibronectin may mediate the Runx3 induced cell shape change of the melanoma cells. Taken together, our findings suggest that Runx3 may regulate cell shape to inhibit melanoma cell migration partly through enhancing stress fiber formation and ECM protein production. Our present study provides further evidence for the idea that cell shape change is potentially correlated with melanoma development and progression.
Insights
Runx3 re-expression in melanoma cells altered cell shape, enhancing stress fibers and fibronectin. This suppressed melanoma cell migration, suggesting Runx3
Area of Science:
- * Molecular biology
- * Cell biology
- * Cancer research
Background:
- * Runx3 is a tumor suppressor gene frequently lost in melanoma.
- * The role of Runx3 loss in melanoma development is not fully understood.
Purpose of the Study:
- * To investigate the functional consequences of Runx3 re-expression in melanoma cells.
- * To explore the relationship between Runx3, cell shape, and melanoma cell migration.
Main Methods:
- * Ectopic re-expression of Runx3 in B16-F10 melanoma cells.
- * Analysis of cell morphology, stress fibers, focal adhesions, and fibronectin expression.
- * Assessment of cell migration and effects of fibronectin coating.
Main Results:
- * Runx3 re-expression induced a change in cell shape, promoting stress fiber formation and focal adhesion maturation.
- * Fibronectin expression was upregulated, and melanoma cell migration was inhibited.
- * Fibronectin partially mediated the Runx3-induced cell shape changes.
Conclusions:
- * Runx3 regulates melanoma cell shape, inhibiting migration via enhanced stress fibers and extracellular matrix production.
- * Cell shape modulation by Runx3 is a potential mechanism influencing melanoma progression.
- * Findings support the link between cell shape and melanoma development.
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