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Monitoring antiangiogenesis of bevacizumab in zebrafish

Bevacizumab, which is a humanized anti-VEGF antibody, has been successfully applied in clinics since 2004. Bevacizumab in combination with chemotherapy showed high safety and has been applied to solid tumors. However, studies on the insight into the mechanism about the antiangiogenesis activity of b...

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Autores principales: Zhang, Jing, Gao, Beili, Zhang, Wenchao, Qian, Zijun, Xiang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084084/
https://www.ncbi.nlm.nih.gov/pubmed/30122900
http://dx.doi.org/10.2147/DDDT.S166330
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author Zhang, Jing
Gao, Beili
Zhang, Wenchao
Qian, Zijun
Xiang, Yi
author_facet Zhang, Jing
Gao, Beili
Zhang, Wenchao
Qian, Zijun
Xiang, Yi
author_sort Zhang, Jing
collection PubMed
description Bevacizumab, which is a humanized anti-VEGF antibody, has been successfully applied in clinics since 2004. Bevacizumab in combination with chemotherapy showed high safety and has been applied to solid tumors. However, studies on the insight into the mechanism about the antiangiogenesis activity of bevacizumab were mostly done on mice models, and so there are no visual and intuitive models to observe the process of antiangiogenesis. Here, we first used a zebrafish model to investigate the angiogenesis suppressing behavior of bevacizumab. Our results showed that bevacizumab inhibited formation of zebrafish subintestinal veins, which mimics the process of tumor angiogenesis in vivo. Meanwhile, bevacizumab caused specific vasculature formation defects in subintestinal veins but not in the trunk. Our study also indicated that bevacizumab could inhibit zebrafish retinal angiogenesis with therapeutic potential.
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spelling pubmed-60840842018-08-17 Monitoring antiangiogenesis of bevacizumab in zebrafish Zhang, Jing Gao, Beili Zhang, Wenchao Qian, Zijun Xiang, Yi Drug Des Devel Ther Methodology Bevacizumab, which is a humanized anti-VEGF antibody, has been successfully applied in clinics since 2004. Bevacizumab in combination with chemotherapy showed high safety and has been applied to solid tumors. However, studies on the insight into the mechanism about the antiangiogenesis activity of bevacizumab were mostly done on mice models, and so there are no visual and intuitive models to observe the process of antiangiogenesis. Here, we first used a zebrafish model to investigate the angiogenesis suppressing behavior of bevacizumab. Our results showed that bevacizumab inhibited formation of zebrafish subintestinal veins, which mimics the process of tumor angiogenesis in vivo. Meanwhile, bevacizumab caused specific vasculature formation defects in subintestinal veins but not in the trunk. Our study also indicated that bevacizumab could inhibit zebrafish retinal angiogenesis with therapeutic potential. Dove Medical Press 2018-08-06 /pmc/articles/PMC6084084/ /pubmed/30122900 http://dx.doi.org/10.2147/DDDT.S166330 Text en © 2018 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Methodology
Zhang, Jing
Gao, Beili
Zhang, Wenchao
Qian, Zijun
Xiang, Yi
Monitoring antiangiogenesis of bevacizumab in zebrafish
title Monitoring antiangiogenesis of bevacizumab in zebrafish
title_full Monitoring antiangiogenesis of bevacizumab in zebrafish
title_fullStr Monitoring antiangiogenesis of bevacizumab in zebrafish
title_full_unstemmed Monitoring antiangiogenesis of bevacizumab in zebrafish
title_short Monitoring antiangiogenesis of bevacizumab in zebrafish
title_sort monitoring antiangiogenesis of bevacizumab in zebrafish
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084084/
https://www.ncbi.nlm.nih.gov/pubmed/30122900
http://dx.doi.org/10.2147/DDDT.S166330
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