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Updated: May 11, 2026

Monitoring Functionality and Morphology of Vasculature Recruited by Factors Secreted by Fast-growing Tumor-generating Cells
Published on: November 23, 2014
Oncogenes and angiogenesis: a way to personalize anti-angiogenic therapy?
Alessia Bottos1, Alberto Bardelli
1Friedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, PO Box 2543, 4058, Basel, Switzerland, alessia.bottos@fmi.ch.
Abstract:
The acquisition of oncogenic mutations and promotion of angiogenesis are key hallmarks of cancer. These features are often thought of as separate events in tumor progression and the two fields of research have frequently been considered as independent. However, as we highlight in this review, activated oncogenes and deregulated angiogenesis are tightly associated, as mutations in cancer cells can lead to perturbation of the pro- and anti-angiogenic balance thereby causing aberrant angiogenesis. We propose that normalization of the vascular network by targeting oncogenes in the tumor cells might lead to more efficient and sustained therapeutic effects compared to therapies targeting tumor vessels. We discuss how pharmacological inhibition of oncogenes in tumor cells restores a functional vasculature by bystander anti-angiogenic effect. As genetic alterations are tumor-specific, targeted therapy, which potentially blocks the angiogenic program activated by individual oncogenes may lead to personalized anti-angiogenic therapy.
Insights
Targeting oncogenes in cancer cells can normalize tumor vasculature, offering a personalized approach to anti-angiogenic therapy. This strategy may yield more effective and sustained treatment outcomes than targeting tumor vessels directly.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Oncogenic mutations and angiogenesis are critical hallmarks of cancer.
- These processes have traditionally been studied as independent events in tumor progression.
Purpose of the Study:
- To review the intricate association between activated oncogenes and deregulated angiogenesis.
- To propose targeting oncogenes within tumor cells as a strategy for normalizing tumor vasculature and enhancing therapeutic effects.
Main Methods:
- Review of existing literature on oncogene activation and angiogenesis.
- Discussion of the mechanisms by which oncogene inhibition impacts tumor vasculature.
- Exploration of personalized anti-angiogenic therapy based on tumor-specific genetic alterations.
Main Results:
- Activated oncogenes are tightly linked to aberrant angiogenesis due to perturbations in the pro- and anti-angiogenic balance.
- Pharmacological inhibition of oncogenes in tumor cells can restore functional vasculature via a bystander anti-angiogenic effect.
- Tumor-specific genetic alterations suggest potential for personalized anti-angiogenic therapies targeting individual oncogenes.
Conclusions:
- Targeting oncogenes within tumor cells offers a promising strategy for normalizing the tumor vascular network.
- This approach may lead to more efficient and sustained therapeutic outcomes compared to direct targeting of tumor vessels.
- Personalized anti-angiogenic therapy, guided by tumor-specific oncogenic profiles, holds potential for improved cancer treatment.
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