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Updated: Jun 2, 2026

Modified In Vivo Matrix Gel Plug Assay for Angiogenesis Studies
Published on: June 30, 2023
VEGF and angiopoietin signaling in tumor angiogenesis and metastasis
Pipsa Saharinen1, Lauri Eklund, Kristina Pulkki
1Molecular/Cancer Biology, Research Programs Unit, Biomedicum Helsinki, P.O.B. 63, (Haartmaninkatu 8), FIN-00014, University of Helsinki, Finland.
Abstract:
Solid tumors require blood vessels for growth and dissemination, and lymphatic vessels as additional conduits for metastatic spread. The identification of growth factor receptor pathways regulating angiogenesis has led to the clinical approval of the first antiangiogenic molecules targeted against the vascular endothelial growth factor (VEGF)-VEGF receptor (VEGFR)-2 pathway. However, in many cases resistance to anti-VEGF-VEGFR therapy occurs, and thus far the clinical benefit has been limited to only modest improvements in overall survival. Therefore, novel treatment modalities are required. Here, we discuss the members of the VEGF-VEGFR family as well as the angiopoietin growth factors and their Tie receptors as potential novel targets for antiangiogenic and antilymphangiogenic therapies.
Insights
New antiangiogenic therapies targeting VEGF-VEGFR pathways are needed due to resistance. Angiopoietin growth factors and Tie receptors offer promising alternative targets for anti-cancer treatments.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Solid tumors depend on blood and lymphatic vessels for growth and metastasis.
- Antiangiogenic therapies targeting the vascular endothelial growth factor (VEGF)-VEGF receptor (VEGFR)-2 pathway have been approved but show limited clinical benefit due to resistance.
- Novel therapeutic strategies are essential to overcome treatment resistance and improve patient outcomes.
Purpose of the Study:
- To explore novel therapeutic targets for antiangiogenic and antilymphangiogenic therapies.
- To discuss the potential of VEGF-VEGFR family members and angiopoietin growth factors/Tie receptors as targets.
Main Methods:
- Review of current literature on angiogenesis and lymphangiogenesis.
- Analysis of the VEGF-VEGFR and angiopoietin-Tie signaling pathways.
- Discussion of potential therapeutic strategies targeting these pathways.
Main Results:
- Limited efficacy and resistance observed with current anti-VEGF-VEGFR therapies.
- Identification of angiopoietin growth factors and their Tie receptors as potential alternative targets.
- VEGF-VEGFR family members and angiopoietin-Tie signaling represent promising avenues for novel anti-cancer treatments.
Conclusions:
- Current antiangiogenic therapies have limitations, necessitating the exploration of new targets.
- Angiopoietin growth factors and Tie receptors present viable targets for developing novel antiangiogenic and antilymphangiogenic treatments.
- Targeting these pathways could lead to improved therapeutic outcomes in cancer treatment.
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