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Updated: Jun 4, 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
Concise review: Dissecting a discrepancy in the literature: do mesenchymal stem cells support or suppress tumor
Ann H Klopp1, Anshul Gupta, Erika Spaeth
1Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA. aklopp@mdanderson.org
Abstract:
The discovery that mesenchymal stem cells (MSCs) are recruited into tumors has led to a great deal of interest over the past decade in the function of MSCs in tumors. To address this, investigators have used a variety of tumor models in which MSCs are added exogenously to determine their impact on tumor development. Interestingly, many studies have reported contradicting results, with some investigators finding that MSCs promote tumor growth and others reporting that MSCs inhibit tumor growth. Many mechanisms have been reported to account for these observations, such as chemokine signaling, modulation of apoptosis, vascular support, and immune modulation. In this review, we analyzed the differences in the methodology of the studies reported and found that the timing of MSC introduction into tumors may be a critical element. Understanding the conditions in which MSCs enhance tumor growth and metastasis is crucial, both to safely develop MSCs as a therapeutic tool and to advance our understanding of the role of tumor stroma in carcinogenesis.
Insights
Mesenchymal stem cells (MSCs) have contradictory effects on tumor growth. This review highlights that the timing of MSC introduction into tumors is a critical factor influencing whether they promote or inhibit cancer progression.
Area of Science:
- Oncology
- Stem Cell Biology
- Cancer Research
Background:
- Mesenchymal stem cells (MSCs) are recruited into tumors, prompting extensive research into their role.
- Studies report conflicting results: MSCs can either promote or inhibit tumor development.
- Potential mechanisms include chemokine signaling, apoptosis modulation, vascular support, and immune modulation.
Purpose of the Study:
- To analyze methodological differences in studies investigating MSCs in tumors.
- To identify critical factors influencing MSCs' pro- or anti-tumorigenic effects.
- To understand the role of tumor stroma in carcinogenesis and inform MSC-based therapies.
Main Methods:
- Review of existing literature on exogenous mesenchymal stem cell administration in various tumor models.
- Comparative analysis of study methodologies, focusing on the timing of MSC introduction.
- Synthesis of reported mechanisms underlying MSC-mediated tumor promotion or inhibition.
Main Results:
- Contradictory findings in the literature regarding MSCs' impact on tumor growth.
- Identified the timing of MSC introduction as a potentially critical variable.
- Highlighted diverse mechanisms like chemokine signaling, apoptosis, vascular, and immune modulation.
Conclusions:
- The timing of mesenchymal stem cell introduction is a key determinant of their effect on tumor growth and metastasis.
- Further research is needed to elucidate conditions under which MSCs enhance or inhibit cancer.
- Understanding these dynamics is crucial for developing safe MSC-based therapies and advancing cancer stroma research.
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