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Meningioma Tumor Microenvironment.
Sajad Sahab-Negah1,2, Ali Gorji3,4,5,6
1Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Advances in Experimental Medicine and Biology
|June 29, 2021
Summary
The tumor microenvironment, crucial for tumor growth, is poorly understood in meningioma, the most common benign brain tumor. This review explores its role in meningioma development and potential new treatments.
Area of Science:
- Oncology
- Neuro-oncology
- Cancer Biology
Background:
- The tumor microenvironment comprises noncancerous cells, extracellular matrix, and proteins that influence tumor progression.
- Meningioma is the most common primary benign intracranial tumor.
- The specific components and functions of the meningioma tumor microenvironment are largely unknown.
Purpose of the Study:
- To review the current understanding of the tumor microenvironment in meningioma.
- To discuss the significance of the tumor microenvironment in meningioma tumorigenesis.
- To highlight potential therapeutic strategies targeting the meningioma microenvironment.
Main Methods:
- Literature review of existing studies on meningioma and tumor microenvironment.
- Synthesis of current knowledge on cellular and molecular components.
- Analysis of the role of the microenvironment in tumor development and treatment.
Main Results:
- The tumor microenvironment significantly influences meningioma behavior and progression.
- Immune cells and fibroblasts within the microenvironment play key roles.
- Understanding these interactions is vital for developing targeted therapies.
Conclusions:
- Further research into the meningioma tumor microenvironment is essential.
- Targeting the microenvironment offers promising avenues for novel therapeutic approaches.
- This review provides a foundation for future investigations into meningioma treatment.
Keywords:
CancerExtracellular matrixGrowth factorsImmune cellsImmune responseInflammationMacrophagesNitric oxide synthasePeripheral immune toleranceStromaT cellsTumor angiogenesis apoptosisTumor infiltrationVascular endothelial growth factor
