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Updated: May 23, 2026

Tumor Treating Field Therapy in Combination with Bevacizumab for the Treatment of Recurrent Glioblastoma
Published on: October 27, 2014
A novel treatment for glioblastoma: integrin inhibition
Marc C Chamberlain1, Timothy Cloughsey, David A Reardon
1Department of Neurology & Neurological Surgery, Division of Neuro-Oncology, University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, 825 Eastlake Avenue E, MS G-4940, Seattle, WA 98109-1023, USA. chambemc@uw.edu
Abstract:
Glioblastoma (GBM) is the most common malignant primary brain tumor, which despite combined modality treatment, recurs and is invariably fatal. New therapies for GBM represent an unmet need in neuro-oncology. This review provides an overview of the epidemiology and molecular biology of GBM and focuses, in particular, on integrins, which are heterodimeric transmembrane surface proteins that, when activated, signal through several GBM-relevant pathways, including proliferation, motility, cytoskeleton organization, survival and angiogenesis pathways. Consequently, the potential effects of anti-integrin strategies in anti-GBM therapeutics are threefold: antiangiogenesis; anti-invasion; and anti-tumor. Trials of anti-integrins are most mature in GBM, and this review summarizes the completed and future trials of integrin inhibitors in the treatment of both newly diagnosed and recurrent GBM.
Insights
New therapies targeting integrins show promise for treating glioblastoma (GBM), the most common malignant brain tumor. Anti-integrin strategies offer potential anti-angiogenesis, anti-invasion, and anti-tumor effects for GBM patients.
Area of Science:
- Neuro-oncology
- Molecular biology
- Cancer research
Background:
- Glioblastoma (GBM) is the most common and fatal primary brain tumor.
- Current treatments offer limited efficacy, highlighting the need for novel therapeutic strategies.
- Integrins play crucial roles in GBM cell signaling, proliferation, motility, and angiogenesis.
Purpose of the Study:
- To review the epidemiology and molecular biology of GBM.
- To focus on the role of integrins in GBM.
- To summarize the therapeutic potential of anti-integrin strategies and ongoing clinical trials in GBM.
Main Methods:
- Literature review of GBM epidemiology and molecular pathways.
- Detailed analysis of integrin function in GBM.
- Summary of completed and future clinical trials involving integrin inhibitors for GBM.
Main Results:
- Integrins are key mediators of GBM-relevant pathways including proliferation, motility, survival, and angiogenesis.
- Anti-integrin strategies demonstrate potential for anti-angiogenesis, anti-invasion, and anti-tumor effects.
- Clinical trials of integrin inhibitors are most advanced in GBM, with ongoing studies for newly diagnosed and recurrent disease.
Conclusions:
- Integrin inhibitors represent a promising therapeutic avenue for glioblastoma.
- Targeting integrins offers a multi-faceted approach to combatting GBM.
- Further clinical investigation of integrin-targeted therapies is warranted for GBM treatment.
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