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Updated: Oct 16, 2025

A Preclinical Mouse Model of Osteosarcoma to Define the Extracellular Vesicle-mediated Communication Between Tumor and Mesenchymal Stem Cells
Published on: May 6, 2018
Mesenchymal Stem Cells and Extracellular Vesicles in Osteosarcoma Pathogenesis and Therapy
Virinder Kaur Sarhadi1, Ravindra Daddali1, Riitta Seppänen-Kaijansinkko1
1Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital, 00014 Helsinki, Finland.
Mesenchymal stem cells (MSCs) and their extracellular vesicles (EVs) play a key role in osteosarcoma (OS) progression and metastasis. MSC-derived EVs offer potential for novel therapeutic strategies against this aggressive bone cancer.
Area of Science:
- Oncology
- Stem Cell Biology
- Biomedical Engineering
Background:
- Osteosarcoma (OS) is a highly aggressive bone tumor in children and adolescents with poor prognosis due to relapse and metastasis.
- The genetic complexity of OS hinders the identification of effective therapeutic targets.
- Mesenchymal stem cells (MSCs) are implicated in OS development and progression through paracrine signaling and interaction with tumor cells.
Purpose of the Study:
- To review the multifaceted role of MSCs in osteosarcoma (OS) pathogenesis.
- To elucidate the function of extracellular vesicles (EVs) secreted by OS cells and MSCs in tumor progression.
- To explore the therapeutic potential of MSC-derived EVs in OS treatment.
Main Methods:
- Literature review focusing on the interaction between MSCs and OS cells.
- Analysis of the role of extracellular vesicles (EVs) in intercellular communication within the OS tumor microenvironment.
- Evaluation of current and potential therapeutic applications of MSC-EVs in OS.
Main Results:
- MSCs influence OS progression by affecting tumor cell proliferation, invasion, angiogenesis, immune response, and metastasis via paracrine signaling.
- Extracellular vesicles (EVs) mediate intercellular communication, transferring functional molecules like miRNAs and proteins, thereby driving OS progression.
- MSC-derived EVs exhibit dual roles, with both pro-tumor and anti-tumor effects, and can be engineered for targeted anti-cancer delivery.
Conclusions:
- MSCs significantly contribute to osteosarcoma (OS) pathogenesis through complex interactions and EV-mediated communication.
- EVs secreted by MSCs and OS cells are critical mediators in the OS tumor microenvironment.
- Engineered MSC-derived EVs represent a promising avenue for developing innovative therapeutic strategies against osteosarcoma.
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