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.

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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