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Updated: May 10, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
Published on: March 20, 2026
Antibody-based antiangiogenic and antilymphangiogenic therapies to prevent tumor growth and progression
Monika Bzowska1, Renata Mężyk-Kopeć, Tomasz Próchnicki
1Department of Cell Biochemistry, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Kraków, Poland.
Abstract:
Blood and lymphatic vessel formation is an indispensable factor for cancer progression and metastasis. Therefore, various strategies designed to block angiogenesis and lymphangiogenesis are being investigated in the hope to arrest and reverse tumor development. Monoclonal antibodies, owing to their unequalled diversity and specificity, might be applied to selectively inhibit the pathways that cancer cells utilize to build up a network of blood vessels and lymphatics. Among the possible targets of antibody-based therapies are proangiogenic and prolymphangiogenic growth factors from the VEGF family and the receptors to which they bind (VEGFRs). Here, we present molecular mechanisms of angiogenesis and lymphangiogenesis exploited by tumors to progress and metastasise, with examples of antibody-based therapeutic agents directed at interfering with these processes. The expanding knowledge of vascular biology helps to explain some of the problems encountered in such therapies, that arise due to the redundancy in signaling networks controlling the formation of blood and lymphatic vessels, and lead to tumor drug resistance. Nonetheless, combined treatments and treatments focused on newly discovered proangiogenic and prolymphangiogenic factors give hope that more prominent therapeutic effects might be achieved in the future.
Insights
Monoclonal antibodies targeting blood and lymphatic vessel growth factors offer a promising strategy to inhibit cancer progression and metastasis. Research explores these therapies to overcome challenges like tumor drug resistance and improve cancer treatment outcomes.
Area of Science:
- Oncology
- Vascular Biology
- Immunotherapy
Background:
- Tumor angiogenesis and lymphangiogenesis are critical for cancer growth and metastasis.
- Strategies to inhibit these processes are under investigation to halt tumor development.
- Monoclonal antibodies present a specific approach to target tumor vascularization pathways.
Purpose of the Study:
- To review the molecular mechanisms of tumor-driven angiogenesis and lymphangiogenesis.
- To discuss antibody-based therapeutic agents targeting these vascularization processes.
- To explore challenges and future directions in anti-angiogenic and anti-lymphangiogenic therapies.
Main Methods:
- Review of molecular mechanisms of angiogenesis and lymphangiogenesis in cancer.
- Analysis of antibody-based therapeutic strategies targeting VEGF family and VEGFRs.
- Discussion of challenges in vascular targeting therapies, including drug resistance.
Main Results:
- Tumors exploit specific molecular pathways for blood and lymphatic vessel formation.
- Antibody-based therapies targeting VEGF/VEGFRs show potential in preclinical and clinical settings.
- Signaling network redundancy contributes to therapeutic resistance in anti-angiogenic treatments.
Conclusions:
- Targeting tumor vascularization with monoclonal antibodies is a key strategy in cancer therapy.
- Understanding vascular biology is crucial for overcoming drug resistance and improving treatment efficacy.
- Combined and novel targeted therapies hold promise for enhanced therapeutic effects in cancer treatment.
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