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Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
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Immune response in glioma's microenvironment.

Houminji Chen1,2, Ming Li3, Yanwu Guo1

  • 1The Second School of Clinical Medicine, Southern Medical University, Guangzhou, P. R. China.

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|January 29, 2021
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Summary
This summary is machine-generated.

This review explores glioma's tumor microenvironment (TME) and its immunobiological factors. Understanding these interactions offers new targets for inhibiting glioma development and improving brain tumor treatments.

Keywords:
cytokinesgliomaimmunoregulatory factorsmacrophagesmicrogliamyeloid-derived suppressor cellstumor microenvironment

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Area of Science:

  • Neuro-oncology
  • Immunology
  • Cancer Biology

Background:

  • Glioma cells interact with the tumor microenvironment (TME), involving immune cells like microglia, macrophages, myeloid-derived suppressor cells (MDSCs), and T lymphocytes.
  • Microglia are particularly significant in promoting glioma growth, while infiltrating immune cells contribute to immune escape through cytokine and chemokine production.
  • Tumor cell interactions within the TME drive glioma heterogeneity and poor patient prognosis.

Purpose of the Study:

  • To review the immunobiological factors influencing glioma development.
  • To identify potential therapeutic targets within the glioma TME.
  • To provide insights into future research and treatment strategies for gliomas.

Main Methods:

  • Comprehensive literature review of immunobiological factors in glioma.
  • Analysis of immune cell interactions within the glioma TME.
  • Examination of current glioma immunotherapy approaches.

Main Results:

  • Identification of key immunobiological factors and immune cells mediating glioma progression.
  • Elucidation of mechanisms contributing to immune evasion in malignant gliomas.
  • Highlighting the role of TME complexity in tumor heterogeneity.

Conclusions:

  • Understanding glioma-TME interactions is crucial for developing novel therapeutic strategies.
  • Targeting specific immunobiological factors and immune cells presents promising avenues for glioma treatment.
  • Further research into these interactions will advance brain tumor immunotherapy.