Related Experiment Video
Updated: Jun 19, 2026

Processing of Primary Brain Tumor Tissue for Stem Cell Assays and Flow Sorting
Published on: September 25, 2012
Cancer stem cells and the biology of brain tumors
Debora Gazzana Flores1, Pitia Flores Ledur, Ana Lucia Abujamra
1Department of Biophysics, Federal University of Rio Grande do Sul (UFRGS), Av. Bento Gonçalves, 9500, Predio 43431, Sala 107, 91501-970, Porto Alegre, RS, Brazil.
Abstract:
There is now compelling evidence that brain tumors harbor a small population of cells characterized by their ability to undergo self-renewal and initiate tumors, termed cancer stem cells (CSCs). The development of therapeutic strategies targeted towards CSC signaling may improve the treatment of brain tumors such as malignant gliomas and medulloblastomas. Here we review the role of cancer stem cells in glioma and medulloblastoma and some of the signaling mechanisms involved in brain tumor stem cell (BTSC) biology, and discuss how these signaling pathways may represent new stem cell targets for the treatment of brain tumors. In addition, we provide illustrative immunohistochemical data on the presence of BTSCs in human gliomas and medulloblastomas, and show preliminary findings suggesting the involvement of a GPCR, the gastrin-releasing peptide receptor (GRPR), in the expansion of BTSCs in vitro.
Insights
Cancer stem cells (CSCs) drive brain tumor growth. Targeting their signaling pathways, like the gastrin-releasing peptide receptor (GRPR), offers new therapeutic strategies for malignant gliomas and medulloblastomas.
Area of Science:
- Neuro-oncology
- Cancer Stem Cell Biology
- Molecular Signaling
Background:
- Brain tumors contain cancer stem cells (CSCs) responsible for tumor initiation and self-renewal.
- Targeting CSC signaling pathways is crucial for developing effective brain tumor treatments.
- Malignant gliomas and medulloblastomas are key brain tumor types where CSCs play a significant role.
Purpose of the Study:
- To review the role of CSCs in glioma and medulloblastoma.
- To explore signaling mechanisms in brain tumor stem cell (BTSC) biology.
- To identify potential new therapeutic targets for brain tumors based on BTSC signaling.
Main Methods:
- Literature review of CSCs in brain tumors.
- Immunohistochemical analysis of BTSCs in human glioma and medulloblastoma samples.
- In vitro experiments investigating the role of gastrin-releasing peptide receptor (GRPR) in BTSC expansion.
Main Results:
- CSCs are a critical component of brain tumors like gliomas and medulloblastomas.
- Specific signaling pathways are implicated in BTSC biology and expansion.
- Preliminary data suggest the gastrin-releasing peptide receptor (GRPR) is involved in BTSC expansion in vitro.
Conclusions:
- Understanding BTSC biology is key to advancing brain tumor therapeutics.
- Signaling pathways, including GRPR, represent promising targets for novel anti-brain tumor strategies.
- Targeted therapies against CSCs hold potential for improved treatment outcomes in malignant gliomas and medulloblastomas.
Related Concept Videos
Cancer Stem Cells and Tumor Maintenance
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Cancer Stem Cells and Tumor Maintenance
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
Distinctive Features of Adult Stem Cells vs Cancer Stem Cells
Adult stem cells
Adult stem cells are tissue-specific; hence, they divide to develop the tissue from which they originate. One type of adult stem cell is the epithelial stem cell, which gives rise to the keratinocytes in the multiple layers of epithelial cells in the epidermis of the skin. Adult bone marrow has three distinct types of stem cells:...
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
The Tumor Microenvironment
Cancer

