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Updated: Apr 20, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
Published on: March 20, 2026
The emerging quest for the optimal angiostatic combination therapy
Arjan W Griffioen1, Andrea Weiss, Robert H Berndsen
1*Angiogenesis Laboratory, Department of Medical Oncology, VU Medical Center, De Boelelaan 1117, 1081HV Amsterdam, The Netherlands.
Abstract:
Angiostatic therapies are now routinely embedded in the daily clinical management of cancer. Although these agents clearly benefit patient survival rates, the effect is only moderate with sometimes considerable side effects. A major cause of failure in this respect is the induction of resistance and tolerability against these drugs. Most angiostatic drugs are tyrosine kinase inhibitors that aim to inhibit or neutralize the activity of tumour-produced growth factors. Frustrating the tumour cells in this way results in genetic adaptations in the cells, turning them into mutants that are dependent on other growth mechanisms. It may therefore be necessary to shift to another class of drugs that directly target the tumour vasculature. It is evident that improvement of future angiogenesis inhibitors can only arise from two efforts. First, through the identification of better targets, preferably specifically expressed in the tumour vasculature. Secondly, through the development of combination therapies. The present review highlights the current efforts and challenges in trying to develop effective angiostatic combination therapies.
Insights
Angiostatic therapies offer moderate cancer survival benefits but face resistance. Future improvements require identifying new targets and developing combination therapies for better angiostatic drug efficacy.
Area of Science:
- Oncology
- Pharmacology
- Cancer Biology
Background:
- Angiostatic therapies are standard in cancer care, improving survival but with limitations.
- Resistance and side effects are major challenges, often due to tumor cells adapting to tyrosine kinase inhibitors.
- Current therapies target tumor-produced growth factors, leading to genetic adaptations in cancer cells.
Purpose of the Study:
- To review current efforts and challenges in developing effective angiostatic combination therapies.
- To highlight the need for improved angiogenesis inhibitors.
- To discuss strategies for overcoming drug resistance in cancer treatment.
Main Methods:
- Literature review of current research on angiostatic therapies.
- Analysis of mechanisms of resistance and tolerability to anti-angiogenic drugs.
- Exploration of novel therapeutic targets and combination strategies.
Main Results:
- Angiostatic therapies provide moderate survival benefits but are hampered by resistance and side effects.
- Tumor cells develop resistance by adapting to tyrosine kinase inhibitors, necessitating alternative approaches.
- Development of new therapies requires identifying specific tumor vasculature targets and combination treatments.
Conclusions:
- Improving angiostatic therapies necessitates identifying novel, tumor vasculature-specific targets.
- Combination therapies are crucial for enhancing efficacy and overcoming resistance.
- Future research should focus on developing advanced angiogenesis inhibitors and combination strategies.
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