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Updated: May 22, 2026

Intravascular Delivery of Biologics to the Rat Kidney
Published on: September 1, 2016
VEGF inhibition, hypertension, and renal toxicity
Suzanne R Hayman1, Nelson Leung, Joseph P Grande
1Department of Internal Medicine, Division of Hematology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA. Hayman.suzanne@mayo.edu
Abstract:
The use of anti-angiogenic agents as part of the therapeutic armamentarium for advanced stage solid tumors has become the standard of care in several instances, particularly for renal cell carcinoma, non-small cell lung carcinoma, colorectal carcinoma, and gastrointestinal stromal tumors. These agents primarily target vascular endothelial growth factor (VEGF) and/or its receptors, and include bevacizumab, a humanized monoclonal antibody against VEGF, as well as tyrosine kinase inhibitors that target several receptor tyrosine kinases (RTK), including VEGF receptors. These therapies, as a general class of anti-angiogenic medications, have been shown to have common adverse vascular effects attributable directly or indirectly to their anti-VEGF effects, including hypertension, renal vascular injury, often manifested by proteinuria and thrombotic microangiopathy, and congestive heart failure. Knowledge of these common side effects and their underlying mechanisms may allow for more accurate and prompt diagnoses, timely clinical interventions, and the development of rational and standard treatments. These measures may minimize patient morbidity and mortality, not only by the treatment of side effects, but also by minimizing the disruption of treatment of the underlying malignancy, as well as improving patient quality of life.
Insights
Anti-angiogenic agents targeting vascular endothelial growth factor (VEGF) are standard cancer treatments. Understanding their common vascular side effects like hypertension and heart failure is crucial for patient care.
Area of Science:
- Oncology
- Pharmacology
- Vascular Biology
Background:
- Anti-angiogenic agents targeting vascular endothelial growth factor (VEGF) are integral to treating advanced solid tumors, including renal cell carcinoma, non-small cell lung carcinoma, colorectal carcinoma, and gastrointestinal stromal tumors.
- These therapies include monoclonal antibodies like bevacizumab and tyrosine kinase inhibitors (TKIs) that target VEGF and its receptors.
- Common adverse effects are vascular, linked to anti-VEGF activity, necessitating a thorough understanding for effective management.
Purpose of the Study:
- To review the common vascular adverse effects of anti-angiogenic therapies.
- To elucidate the underlying mechanisms of these side effects.
- To emphasize the importance of prompt diagnosis and management for improved patient outcomes.
Main Methods:
- Review of literature on anti-angiogenic agents and their adverse vascular effects.
- Analysis of mechanisms linking anti-VEGF activity to specific toxicities.
- Synthesis of information for clinical application in managing side effects.
Main Results:
- Common adverse vascular effects include hypertension, renal vascular injury (proteinuria, thrombotic microangiopathy), and congestive heart failure.
- These effects are directly or indirectly related to the inhibition of VEGF signaling.
- Understanding these mechanisms aids in early detection and intervention.
Conclusions:
- Knowledge of anti-angiogenic agent side effects is vital for oncologists and healthcare providers.
- Timely diagnosis and management of vascular toxicities can minimize morbidity and mortality.
- Effective side effect management can improve patient quality of life and treatment adherence for underlying malignancies.
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