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Updated: Jul 2, 2025

A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
Glioblastoma-Associated Mesenchymal Stem/Stromal Cells and Cancer-Associated Fibroblasts: Partners in Crime?
Thibault Lootens1,2,3, Bart I Roman3,4, Christian V Stevens3,4
14Brain, Department of Head and Skin, Ghent University, 9000 Ghent, Belgium.
Abstract:
Tumor-associated mesenchymal stem/stromal cells (TA-MSCs) have been recognized as attractive therapeutic targets in several cancer types, due to their ability to enhance tumor growth and angiogenesis and their contribution to an immunosuppressive tumor microenvironment (TME). In glioblastoma (GB), mesenchymal stem cells (MSCs) seem to be recruited to the tumor site, where they differentiate into glioblastoma-associated mesenchymal stem/stromal cells (GA-MSCs) under the influence of tumor cells and the TME. GA-MSCs are reported to exert important protumoral functions, such as promoting tumor growth and invasion, increasing angiogenesis, stimulating glioblastoma stem cell (GSC) proliferation and stemness, mediating resistance to therapy and contributing to an immunosuppressive TME. Moreover, they could act as precursor cells for cancer-associated fibroblasts (CAFs), which have recently been identified in GB. In this review, we provide an overview of the different functions exerted by GA-MSCs and CAFs and the current knowledge on the relationship between these cell types. Increasing our understanding of the interactions and signaling pathways in relevant models might contribute to future regimens targeting GA-MSCs and GB-associated CAFs to inhibit tumor growth and render the TME less immunosuppressive.
Insights
Tumor-associated mesenchymal stem cells in glioblastoma promote tumor growth and therapy resistance. Targeting these cells and cancer-associated fibroblasts may offer new glioblastoma treatment strategies.
Area of Science:
- Oncology
- Cancer Biology
- Immunology
Background:
- Tumor-associated mesenchymal stem/stromal cells (TA-MSCs) promote tumor growth, angiogenesis, and immunosuppression.
- In glioblastoma (GB), mesenchymal stem cells (MSCs) differentiate into glioblastoma-associated MSCs (GA-MSCs) within the tumor microenvironment (TME).
Purpose of the Study:
- To review the protumoral functions of GA-MSCs and cancer-associated fibroblasts (CAFs) in glioblastoma.
- To explore the relationship between GA-MSCs and CAFs in the glioblastoma TME.
Main Methods:
- Literature review of existing research on GA-MSCs and CAFs in glioblastoma.
- Analysis of cellular interactions and signaling pathways within the glioblastoma TME.
Main Results:
- GA-MSCs promote glioblastoma growth, invasion, angiogenesis, and therapy resistance.
- GA-MSCs contribute to an immunosuppressive TME and may act as precursors to CAFs.
- CAFs are identified in glioblastoma and likely play a role in tumor progression.
Conclusions:
- Understanding GA-MSC and CAF functions and interactions is crucial for glioblastoma treatment.
- Targeting GA-MSCs and CAFs could inhibit tumor growth and overcome TME-mediated immunosuppression.
- Further research into signaling pathways may lead to novel therapeutic strategies for glioblastoma.
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