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Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo

Acoustically stimulated microbubbles have been demonstrated to perturb endothelial cells of the vasculature resulting in biological effects. In the present study, vascular and tumor response to ultrasound-stimulated microbubble and radiation treatment was investigated in vivo to identify effects on...

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Autores principales: Lai, Priscilla, Tarapacki, Christine, Tran, William T., El Kaffas, Ahmed, Lee, Justin, Hupple, Clinton, Iradji, Sarah, Giles, Anoja, Al-Mahrouki, Azza, Czarnota, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872648/
https://www.ncbi.nlm.nih.gov/pubmed/27226983
http://dx.doi.org/10.18632/oncoscience.299
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author Lai, Priscilla
Tarapacki, Christine
Tran, William T.
El Kaffas, Ahmed
Lee, Justin
Hupple, Clinton
Iradji, Sarah
Giles, Anoja
Al-Mahrouki, Azza
Czarnota, Gregory J.
author_facet Lai, Priscilla
Tarapacki, Christine
Tran, William T.
El Kaffas, Ahmed
Lee, Justin
Hupple, Clinton
Iradji, Sarah
Giles, Anoja
Al-Mahrouki, Azza
Czarnota, Gregory J.
author_sort Lai, Priscilla
collection PubMed
description Acoustically stimulated microbubbles have been demonstrated to perturb endothelial cells of the vasculature resulting in biological effects. In the present study, vascular and tumor response to ultrasound-stimulated microbubble and radiation treatment was investigated in vivo to identify effects on the blood vessel endothelium. Mice bearing breast cancer tumors (MDA-MB-231) were exposed to ultrasound after intravenous injection of microbubbles at different concentrations, and radiation at different doses (0, 2, and 8 Gy). Mice were sacrificed 12 and 24 hours after treatment for histopathological analysis. Tumor growth delay was assessed for up to 28 days after treatment. The results demonstrated additive antitumor and antivascular effects when ultrasound stimulated microbubbles were combined with radiation. Results indicated tumor cell apoptosis, vascular leakage, a decrease in tumor vasculature, a delay in tumor growth and an overall tumor disruption. When coupled with radiation, ultrasound-stimulated microbubbles elicited synergistic anti-tumor and antivascular effects by acting as a radioenhancing agent in breast tumor blood vessels. The present study demonstrates ultrasound driven microbubbles as a novel form of targeted antiangiogenic therapy in a breast cancer xenograft model that can potentiate additive effects to radiation in vivo.
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spelling pubmed-48726482016-05-25 Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo Lai, Priscilla Tarapacki, Christine Tran, William T. El Kaffas, Ahmed Lee, Justin Hupple, Clinton Iradji, Sarah Giles, Anoja Al-Mahrouki, Azza Czarnota, Gregory J. Oncoscience Research Paper Acoustically stimulated microbubbles have been demonstrated to perturb endothelial cells of the vasculature resulting in biological effects. In the present study, vascular and tumor response to ultrasound-stimulated microbubble and radiation treatment was investigated in vivo to identify effects on the blood vessel endothelium. Mice bearing breast cancer tumors (MDA-MB-231) were exposed to ultrasound after intravenous injection of microbubbles at different concentrations, and radiation at different doses (0, 2, and 8 Gy). Mice were sacrificed 12 and 24 hours after treatment for histopathological analysis. Tumor growth delay was assessed for up to 28 days after treatment. The results demonstrated additive antitumor and antivascular effects when ultrasound stimulated microbubbles were combined with radiation. Results indicated tumor cell apoptosis, vascular leakage, a decrease in tumor vasculature, a delay in tumor growth and an overall tumor disruption. When coupled with radiation, ultrasound-stimulated microbubbles elicited synergistic anti-tumor and antivascular effects by acting as a radioenhancing agent in breast tumor blood vessels. The present study demonstrates ultrasound driven microbubbles as a novel form of targeted antiangiogenic therapy in a breast cancer xenograft model that can potentiate additive effects to radiation in vivo. Impact Journals LLC 2016-03-24 /pmc/articles/PMC4872648/ /pubmed/27226983 http://dx.doi.org/10.18632/oncoscience.299 Text en Copyright: © 2016 Lai et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Lai, Priscilla
Tarapacki, Christine
Tran, William T.
El Kaffas, Ahmed
Lee, Justin
Hupple, Clinton
Iradji, Sarah
Giles, Anoja
Al-Mahrouki, Azza
Czarnota, Gregory J.
Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title_full Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title_fullStr Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title_full_unstemmed Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title_short Breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
title_sort breast tumor response to ultrasound mediated excitation of microbubbles and radiation therapy in vivo
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872648/
https://www.ncbi.nlm.nih.gov/pubmed/27226983
http://dx.doi.org/10.18632/oncoscience.299
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