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Updated: Feb 14, 2026

Intratibial Osteosarcoma Cell Injection to Generate Orthotopic Osteosarcoma and Lung Metastasis Mouse Models
Published on: October 28, 2021
MiR-139 prompts the development of osteosarcomas mainly through targeting ROCK1
Abstract:
Abnormal expression of miR-139 was found to be aberrantly expressed in various tumors. However, whether it is involved in osteosarcomas (OS) has never been explored. In the current study, we found that the level of ROCK1 was markedly increased in OS cancer tissues compared to that of noncancerous tissues. Meanwhile, the expression of miR-139 was markedly reduced in OS cancer tissues and cell lines. Enhanced miR-139 expression markedly suppressed colony-formation and cell invasion capacity of OS cancer cells. Dual luciferase reporter assay demonstrated that ROCK1 was a target gene of miR-139. Moreover, overexpression of ROCK1 also led to increased invasion capacity in OS cancer cells even when miR-139 was inhibited, suggesting the anti-invasion effects of miR-139 were mediated through ROCK1. In summary, our present findings indicate that miR-139 functions as a tumor suppressor in OS cancer cells mainly by targeting ROCK1.
Insights
MicroRNA-139 (miR-139) acts as a tumor suppressor in osteosarcoma (OS) by inhibiting ROCK1. This study reveals miR-139
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Aberrant microRNA (miRNA) expression is implicated in various cancers.
- The role of miR-139 in osteosarcoma (OS) development and progression remains unexplored.
Purpose of the Study:
- To investigate the function of miR-139 in osteosarcoma.
- To identify the molecular targets of miR-139 in OS cells.
Main Methods:
- Quantitative real-time PCR to measure miR-139 and ROCK1 expression.
- Cell viability and invasion assays to assess miR-139 function.
- Dual-luciferase reporter assays to confirm ROCK1 as a direct target of miR-139.
Main Results:
- miR-139 expression was significantly downregulated in OS tissues and cell lines.
- ROCK1 expression was markedly upregulated in OS tissues.
- Overexpression of miR-139 suppressed OS cell proliferation and invasion.
- ROCK1 was validated as a direct target of miR-139.
- ROCK1 overexpression reversed the anti-invasive effects of miR-139.
Conclusions:
- miR-139 functions as a tumor suppressor in osteosarcoma.
- The anti-tumor effects of miR-139 in OS are primarily mediated through the inhibition of ROCK1.
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