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Updated: Aug 29, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
Published on: March 20, 2026
Angiogenesis inhibitors: current & future directions
Shaker A Mousa1, Ahmed S Mousa
1Albany College of Pharmacy & Pharmaceutical Research Institute (PRI) at Albany, 106 New Scotland Avenue, Albany, NY 12208-3492, USA. mousas@acp.edu
Abstract:
The field of angiogenesis modulation is at a major crossroad. A tremendous advancement in basic science in this field is providing an excellent support for the concept, which is in contrast to a lack of strong clinical support to date. With regard to the large gap between experimental data and clinical data, the best model of human malignancy is in human cancer patients and the best model of human ocular angiogenesis-mediated disorders such as diabetic retinopathy (DR) and age related macular degeneration (AMD) is in human RD and AMD patients. Additionally, clinical outcomes should include benefit/risk ratios, hard end points (mortality and quality of life as opposed to increased microvascular density with pro-angiogenic agents or tumor size reduction with anti-angiogenesis agents) as well as cost effectiveness. Experimental models should be used to provide guidance, placebo effect, comparative data, and mechanistic understanding as opposed to being used for expected clinical efficacy. We also have to understand existing strategies and how angiogenesis modulation can add further value (i.e. not to replace existing strategy but rather improve efficacy/safety). Recent investigation defined numerous strategies in the modulation of angiogenesis. Those strategies are driven from haemostatic, fibrinolytic, cell adhesion molecules, extracellular matrix, growth factors, and other endogenous systems involved in the modulation of angiogenesis.
Insights
Angiogenesis modulation shows promise in basic science but lacks clinical validation. Human patient models and hard endpoints are crucial for advancing therapies for diseases like diabetic retinopathy and macular degeneration.
Area of Science:
- Focuses on the scientific principles and clinical applications of angiogenesis modulation.
- Explores the discrepancy between experimental findings and clinical outcomes in angiogenesis research.
Background:
- Basic science advancements in angiogenesis modulation are significant.
- Clinical evidence supporting angiogenesis modulation strategies remains limited.
- A gap exists between experimental data and clinical efficacy in human diseases.
Purpose of the Study:
- To highlight the critical need for human-based models in studying angiogenesis-mediated disorders.
- To emphasize the importance of clinical outcome measures, including benefit/risk, hard endpoints, and cost-effectiveness.
- To redefine the role of experimental models in guiding clinical angiogenesis research.
Main Methods:
- Utilizes human cancer patients as models for malignancy.
- Employs human patients with diabetic retinopathy (DR) and age-related macular degeneration (AMD) for ocular angiogenesis studies.
- Advocates for incorporating benefit/risk ratios, mortality, quality of life, and cost-effectiveness in clinical evaluations.
Main Results:
- Experimental models are best suited for mechanistic understanding and guidance, not predicting clinical efficacy.
- Human patient data is essential for validating angiogenesis modulation strategies.
- Numerous angiogenesis modulation strategies have been identified, targeting various biological systems.
Conclusions:
- Human patient-derived data and clinically relevant endpoints are paramount for successful angiogenesis modulation therapies.
- Experimental models should complement, not replace, human studies.
- Future strategies must integrate with existing treatments to improve efficacy and safety.
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