Related Experiment Video
Updated: Mar 25, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
Risk factors of atherosclerosis during systemic therapy targeting vascular endothelial growth factor
Hana Študentová1, Jarmila Indráková2, Pavla Petrová3
1Department of Oncology, Palacký University Medical School and Teaching Hospital, Olomouc 775 20, Czech Republic.
Insights
Vascular endothelial growth factor (VEGF) targeted therapy accelerates atherosclerosis, indicated by increased intima-media thickness (IMT). This therapy also impacts atherosclerosis risk factors and can lead to myocardial ischemia.
Area of Science:
- Cardiovascular Medicine
- Oncology
- Pharmacology
Background:
- Vascular endothelial growth factor (VEGF) is crucial for angiogenesis.
- Anti-VEGF therapies are used in cancer treatment but can have cardiovascular side effects.
- Atherosclerosis is a significant risk factor for cardiovascular events.
Purpose of the Study:
- To investigate the impact of anti-VEGF therapy on intima-media thickness (IMT) and myocardial perfusion.
- To assess changes in laboratory risk factors for atherosclerosis during anti-VEGF treatment.
- To determine if anti-VEGF therapy accelerates atherosclerosis.
Main Methods:
- Studied 58 patients with metastatic colorectal or renal cell carcinoma undergoing anti-VEGF therapy.
- Measured IMT, myocardial perfusion, and laboratory risk factors before and during treatment at 3-month intervals.
- Monitored blood pressure, troponin T, high-density lipoprotein cholesterol, C-reactive protein, and homocysteine levels.
Main Results:
- Intima-media thickness (IMT) consistently increased during anti-VEGF therapy compared to pretreatment levels.
- Transient increases in blood pressure and troponin T were observed.
- Changes in lipid profiles and inflammatory markers included increased HDL cholesterol and decreased C-reactive protein and homocysteine.
- Novel myocardial ischemia was identified in some patients.
Conclusions:
- Anti-VEGF therapy is associated with an acceleration of atherosclerosis, evidenced by increased IMT.
- The therapy alters various laboratory risk factors for atherosclerosis.
- Clinical monitoring for cardiovascular complications is warranted in patients receiving anti-VEGF treatment.
Abstract:
The aim of the present study was to examine the changes in intima-media thickness (IMT) and myocardial perfusion in association with other laboratory risk factors for atherosclerosis in patients treated with therapy that targeted vascular endothelial growth factor (VEGF). IMT, myocardial perfusion and laboratory risk factors of atherosclerosis were studied in 58 patients with metastatic colorectal carcinoma or metastatic renal cell carcinoma prior to and at 3-monthly intervals during anti-VEGF treatment. Compared with the pretreatment IMT, the results indicated that the IMT was consistently increased during therapy in the two patient groups. Patient blood pressure and concentration of troponin T increased transiently. An increase in the concentration of high-density lipoprotein cholesterol and decrease in the concentrations of C-reactive protein and homocysteine were also observed. Novel myocardial ischemia was evident in individual patients. In conclusion, anti-VEGF therapy affects the laboratory risk factors of atherosclerosis and results in an acceleration of atherosclerosis, as demonstrated by increased IMT.
Related Concept Videos
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Regulation of Angiogenesis and Blood Supply
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Therapeutic Drug Monitoring: Affecting Factors
Atherosclerosis III: Management

