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Updated: Jan 20, 2026

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Quantitative Immunohistochemistry of the Cellular Microenvironment in Patient Glioblastoma Resections
Published on: July 31, 2017
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Kinins in Glioblastoma Microenvironment
Mona N Oliveira1,2, Barbara Breznik3, Micheli M Pillat1
1Department of Biochemistry, Institute of Chemistry, University of São Paulo, Av. Prof. Lineus Prestes 748, São Paulo, SP, 05508-000, Brazil.
Summary
Mesenchymal stem cells interact with glioblastoma cells, influencing tumour progression. Kinin signalling, particularly through kinin receptors, plays a key role in this microenvironment and may offer new therapeutic targets.
Area of Science:
- Neuro-oncology
- Cancer Biology
- Stem Cell Biology
Background:
- Tumour progression involves complex interactions between cancer cells, cancer stem cells, and stromal cells.
- Mesenchymal stem cells (MSCs) can migrate to tumours and differentiate, potentially influencing tumour growth.
- Glioblastoma (GBM) has limited therapeutic options, making MSCs a potential cell therapy tool.
Purpose of the Study:
- To review the interactions between MSCs and glioblastoma cells within the tumour microenvironment.
- To highlight the role of kinin signalling and kinin receptors in glioblastoma progression.
- To explore the potential of targeting kinin signalling for glioblastoma therapy.
Main Methods:
- Literature review of studies on MSC-glioblastoma interactions.
- Analysis of the role of microenvironmental cues and kinin receptor signalling.
- Examination of kinin's influence on blood-brain barrier drug transfer and angiogenesis.
Main Results:
- MSCs can either inhibit or support glioblastoma progression.
- Cancer cells exhibit differential responses to microenvironmental cues and kinin signalling.
- Kinin receptor expression increases with glioblastoma malignancy, suggesting a significant role for kinin signalling.
Conclusions:
- Kinin signalling is a crucial, yet under-explored, aspect of the glioblastoma microenvironment.
- Kinins impact drug delivery across the blood-brain barrier and tumour angiogenesis.
- Kinin antagonists show promise as anti-invasive agents for adjuvant glioblastoma therapy.
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