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Updated: Jul 19, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
Published on: March 20, 2026
Galectin-1 is essential in tumor angiogenesis and is a target for antiangiogenesis therapy
Victor L J L Thijssen1, Ruben Postel, Ricardo J M G E Brandwijk
1Angiogenesis Laboratory, Research Institute for Growth and Development (GROW), Department of Pathology, University Maastricht, 6202A2 Maastricht, The Netherlands.
Abstract:
We describe that galectin-1 (gal-1) is a receptor for the angiogenesis inhibitor anginex, and that the protein is crucial for tumor angiogenesis. gal-1 is overexpressed in endothelial cells of different human tumors. Expression knockdown in cultured endothelial cells inhibits cell proliferation and migration. The importance of gal-1 in angiogenesis is illustrated in the zebrafish model, where expression knockdown results in impaired vascular guidance and growth of dysfunctional vessels. The role of gal-1 in tumor angiogenesis is demonstrated in gal-1-null mice, in which tumor growth is markedly impaired because of insufficient tumor angiogenesis. Furthermore, tumor growth in gal-1-null mice no longer responds to antiangiogenesis treatment by anginex. Thus, gal-1 regulates tumor angiogenesis and is a target for angiostatic cancer therapy.
Insights
Galectin-1 (gal-1) acts as a receptor for anginex, a key regulator of tumor angiogenesis. Inhibiting gal-1 significantly impairs tumor growth and vascularization, highlighting its therapeutic potential.
Area of Science:
- Oncology
- Molecular Biology
- Vascular Biology
Background:
- Tumor angiogenesis is essential for tumor growth and metastasis.
- Angiogenesis inhibitors are a promising cancer therapy strategy.
- The specific molecular mechanisms regulating tumor angiogenesis are not fully understood.
Purpose of the Study:
- To investigate the role of galectin-1 (gal-1) in tumor angiogenesis.
- To determine if gal-1 is a receptor for the angiogenesis inhibitor anginex.
- To evaluate gal-1 as a potential therapeutic target for anti-angiogenesis cancer therapy.
Main Methods:
- Galectin-1 (gal-1) expression analysis in tumor endothelial cells.
- Gal-1 knockdown in cultured endothelial cells to assess proliferation and migration.
- Zebrafish model to study the effects of gal-1 knockdown on angiogenesis.
- Tumor growth studies in gal-1-null mice treated with anginex.
Main Results:
- Galectin-1 (gal-1) is overexpressed in endothelial cells of human tumors.
- Gal-1 knockdown inhibits endothelial cell proliferation and migration.
- Gal-1 knockdown in zebrafish impairs vascular development.
- Tumor growth is significantly reduced in gal-1-null mice due to impaired angiogenesis.
- Tumor growth in gal-1-null mice is unresponsive to anginex treatment.
Conclusions:
- Galectin-1 (gal-1) is a crucial regulator of tumor angiogenesis.
- Gal-1 functions as a receptor for the angiogenesis inhibitor anginex.
- Gal-1 represents a novel therapeutic target for anti-angiogenesis cancer strategies.
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