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Updated: May 3, 2026

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells
Published on: May 6, 2018
Exosome-formed synthetic microRNA-143 is transferred to osteosarcoma cells and inhibits their migration
Keisuke Shimbo1, Shigeru Miyaki2, Hiroyuki Ishitobi3
1Department of Orthopedic Surgery, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Abstract:
MicroRNAs (miRNAs) have emerged as potential anticancer agents, but their clinical application is limited by the lack of an effective delivery system to tumors. Exosomes are small vesicles that play important roles in intercellular communication. Here, we show that synthetic miR-143 introduced into cells is released enveloped in exosomes and that the secreted exosome-formed miR-143 is transferred to osteosarcoma cells. The delivery of exosome-formed miR-143 significantly reduced the migration of osteosarcoma cells. The delivery efficiency of exosome-formed miR-143 was less than that achieved with lipofection, but the migratory potential of osteosarcoma cells was similarly inhibited after both strategies. Our results suggest that exosomes can deliver synthetic miR-143 and are a potentially efficient and functional delivery system.
Insights
Synthetic microRNAs (miRNAs) show anticancer promise. Exosomes effectively deliver miR-143 to osteosarcoma cells, inhibiting their migration, suggesting exosomes as a viable delivery system.
Area of Science:
- Biotechnology
- Cancer Research
- Cell Biology
Background:
- MicroRNAs (miRNAs) are investigated as anticancer agents.
- Clinical use of miRNAs is hindered by ineffective tumor delivery systems.
- Exosomes are key mediators of intercellular communication.
Purpose of the Study:
- To investigate exosomes as a delivery system for synthetic microRNAs.
- To evaluate the efficacy of exosome-delivered miR-143 in osteosarcoma cells.
Main Methods:
- Synthetic miR-143 was introduced into cells.
- Exosomes were collected after cells released them.
- Exosome-formed miR-143 was delivered to osteosarcoma cells.
- Cell migration was assessed.
Main Results:
- Synthetic miR-143 was successfully encapsulated and released by exosomes.
- Exosome-mediated delivery of miR-143 inhibited osteosarcoma cell migration.
- While lipofection showed higher delivery efficiency, both methods similarly reduced cell migration.
Conclusions:
- Exosomes can efficiently deliver synthetic miR-143 to target cells.
- Exosome-formed miR-143 demonstrates functional anticancer activity by reducing cell migration.
- Exosomes represent a promising and functional delivery platform for miRNA-based cancer therapy.
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