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Related Concept Videos

Glial Cells01:04

Glial Cells

Overview
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
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Nervous Tissue: Glial Cells01:31

Nervous Tissue: Glial Cells

Glia, or neuroglia, are vital support cells that assist neurons in their functions. The term "glia" originates from the Greek word for "glue," reflecting their role in holding the nervous system together. These cells can be categorized into six types: four in the central nervous system (CNS) and two in the peripheral nervous system (PNS).
The CNS glial cell includes the astrocytes, the oligodendrocytes, the microglia, and the ependymal cells.
Astrocytes are star-shaped glial cells that interact...
Cancer Cell Migration through Invadopodia01:35

Cancer Cell Migration through Invadopodia

Invadosome is a broad category of cell surface structures with proteolytic activity that  degrades the extracellular matrix (ECM). Invadosomes are present in normal cell types, including macrophages, endothelial cells, and neurons, as well as tumor cells. Although the macrophage podosomes and tumor cell invadopodia are classified as invadosomes, they have different structures, molecular pathways, and functions. Podosomes are short structures that last for a few minutes. However, invadopodia can...

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Related Experiment Video

Updated: May 12, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
09:33

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis

Published on: March 20, 2026

Glia-derived VCAM1 promotes glioma progression.

Jiajing Dai1, Hailong Zheng1, Jiaxu Luo1

  • 1Department of Neurobiology, Basic Medical Sciences, Capital Medical University School, Beijing, China.

Frontiers in Oncology
|May 11, 2026
PubMed
Summary

Astrocyte-derived VCAM1 drives glioma progression and impacts survival. Targeting VCAM1 offers a potential therapeutic strategy, but its effectiveness varies with tumor type and location.

Keywords:
VCAM1astrocytegliomaglioma stem cell-like cellstherapeutic target

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Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
12:52

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells

Published on: November 28, 2015

Area of Science:

  • Neuro-oncology
  • Tumor Microenvironment Research
  • Cancer Metastasis

Background:

  • Glioma progression and therapeutic resistance are driven by interactions between cancer cells and the tumor microenvironment (TME).
  • VCAM1 (Vascular Cell Adhesion Molecule 1) is implicated in metastasis in various cancers, but its role in the glioma TME is not well understood.

Purpose of the Study:

  • To investigate the function of VCAM1 in glioma.
  • To correlate VCAM1 expression with patient survival outcomes.
  • To assess the impact of astrocytic VCAM1 ablation on glioma growth and survival.

Main Methods:

  • Analysis of human glioma datasets for VCAM1 expression and survival correlation.
  • Characterization of VCAM1 expression in mouse glioma models (syngeneic and primary).
  • Selective ablation of VCAM1 in GLAST-positive astrocytes in glioma-bearing mice.

Main Results:

  • VCAM1 is highly expressed in proliferative glioma stem cell-like cells (GSLCs) and in TME-associated astrocytes.
  • Selective deletion of astrocytic VCAM1 significantly extended median survival in certain glioma models (e.g., GL261).
  • Survival benefits were dependent on tumor location and genetic background, with limited efficacy in aggressive tumors; clinical data showed VCAM1 correlates with survival in low-grade glioma but not glioblastoma.

Conclusions:

  • Astrocyte-derived VCAM1 is a key factor in glioma progression, facilitating tumor-TME interactions.
  • Targeting VCAM1 signaling is a potential microenvironment-focused therapeutic strategy for glioma.
  • Clinical application of VCAM1 targeting requires consideration of tumor heterogeneity (regional and genetic).