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Updated: Jun 27, 2026

Analyzing Tumor and Tissue Distribution of Target Antigen Specific Therapeutic Antibody
Published on: May 16, 2020
From anti-angiogenesis to anti-lymphangiogenesis: emerging trends in cancer therapy
Steven A Stacker1, Marc G Achen
1Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Victoria, Australia. Steven.stacker@ludwig.edu.au
Abstract:
The theory that angiogenesis could support tumor growth and therefore be a target for cancer therapy was explored in publications by Judah Folkman in the 1970s. This theory was then fostered by Folkman for over 2 decades until, via modern molecular and cell biology techniques, it was vindicated in animal tumor models, and subsequently with the successful clinical trials of a humanized monoclonal antibody which neutralizes vascular endothelial growth factor (VEGF). In the process of proving the "anti-angiogenesis" theory, researchers in vascular, cancer, and developmental biology have gained insight into how the vascular network operates at the molecular level. Following on from the wave of activity that accompanied the study of angiogenesis, some of the molecular mechanisms controlling the related process of lymphangiogenesis have now been identified. The growth of lymphatic vessels was found to be controlled by proteins related to VEGF, namely VEGF-C and VEGF-D, which are associated with a number of human tumor types. The experimental inhibition of this process in animal models has suggested that lymphangiogenic growth factors facilitate the metastatic spread of tumor cells via lymphatics. Unlike the anti-angiogenesis strategy, anti-lymphangiogenesis is yet to be tested clinically; however, the notion that anti-lymphangiogenesis may be beneficial for cancer therapy is supported by extensive data from animal models and clinicopatholgical data. History may show that anti-angiogenesis provided the vantage point from which anti-lymphangiogenesis was seen as a viable concept for targeting tumors and other pathological conditions.
Insights
Targeting tumor blood vessel growth (angiogenesis) is a proven cancer therapy. New research explores inhibiting lymphatic vessel growth (anti-lymphangiogenesis) as a potential cancer treatment, building on anti-angiogenesis insights.
Area of Science:
- Cancer Biology
- Vascular Biology
- Developmental Biology
Background:
- The concept of targeting tumor angiogenesis, or blood vessel formation, emerged in the 1970s.
- Anti-angiogenesis therapy, targeting vascular endothelial growth factor (VEGF), has been validated through animal models and clinical trials.
- Insights from angiogenesis research have advanced understanding of molecular mechanisms in vascular networks.
Purpose of the Study:
- To explore the molecular mechanisms controlling lymphangiogenesis, the formation of lymphatic vessels.
- To investigate the potential of anti-lymphangiogenesis as a cancer therapy, drawing parallels with anti-angiogenesis strategies.
- To evaluate the role of VEGF-C and VEGF-D in tumor progression and metastasis.
Main Methods:
- Review of historical research on angiogenesis and its therapeutic implications.
- Identification of molecular regulators of lymphangiogenesis, including VEGF-C and VEGF-D.
- Analysis of preclinical data from animal models investigating the inhibition of lymphangiogenesis.
Main Results:
- Lymphangiogenesis is regulated by VEGF-C and VEGF-D, which are linked to various human cancers.
- Inhibition of lymphangiogenesis in animal models suggests it hinders tumor cell metastasis via lymphatic spread.
- Extensive preclinical and clinicopathological data support the potential efficacy of anti-lymphangiogenesis.
Conclusions:
- Anti-lymphangiogenesis represents a promising, yet untested clinically, therapeutic strategy for cancer.
- The success of anti-angiogenesis has paved the way for considering anti-lymphangiogenesis targeting.
- Targeting both angiogenesis and lymphangiogenesis may offer novel approaches for cancer treatment.
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