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Focused Ultrasound-enabled Brain Tumor Liquid Biopsy

Although blood-based liquid biopsies have emerged as a promising non-invasive method to detect biomarkers in various cancers, limited progress has been made for brain tumors. One major obstacle is the blood-brain barrier (BBB), which hinders efficient passage of tumor biomarkers into the peripheral...

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Autores principales: Zhu, Lifei, Cheng, Galen, Ye, Dezhuang, Nazeri, Arash, Yue, Yimei, Liu, Weijun, Wang, Xiaowei, Dunn, Gavin P., Petti, Allegra A., Leuthardt, Eric C., Chen, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919906/
https://www.ncbi.nlm.nih.gov/pubmed/29700310
http://dx.doi.org/10.1038/s41598-018-24516-7
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author Zhu, Lifei
Cheng, Galen
Ye, Dezhuang
Nazeri, Arash
Yue, Yimei
Liu, Weijun
Wang, Xiaowei
Dunn, Gavin P.
Petti, Allegra A.
Leuthardt, Eric C.
Chen, Hong
author_facet Zhu, Lifei
Cheng, Galen
Ye, Dezhuang
Nazeri, Arash
Yue, Yimei
Liu, Weijun
Wang, Xiaowei
Dunn, Gavin P.
Petti, Allegra A.
Leuthardt, Eric C.
Chen, Hong
author_sort Zhu, Lifei
collection PubMed
description Although blood-based liquid biopsies have emerged as a promising non-invasive method to detect biomarkers in various cancers, limited progress has been made for brain tumors. One major obstacle is the blood-brain barrier (BBB), which hinders efficient passage of tumor biomarkers into the peripheral circulation. The objective of this study was to determine whether FUS in combination with microbubbles can enhance the release of biomarkers from the brain tumor to the blood circulation. Two glioblastoma tumor models (U87 and GL261), developed by intracranial injection of respective enhanced green fluorescent protein (eGFP)-transduced glioblastoma cells, were treated by FUS in the presence of systemically injected microbubbles. Effect of FUS on plasma eGFP mRNA levels was determined using quantitative polymerase chain reaction. eGFP mRNA were only detectable in the FUS-treated U87 mice and undetectable in the untreated U87 mice (maximum cycle number set to 40). This finding was replicated in GL261 mice across three different acoustic pressures. The circulating levels of eGFP mRNA were 1,500–4,800 fold higher in the FUS-treated GL261 mice than that of the untreated mice for the three acoustic pressures. This study demonstrated the feasibility of FUS-enabled brain tumor liquid biopsies in two different murine glioma models across different acoustic pressures.
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spelling pubmed-59199062018-05-01 Focused Ultrasound-enabled Brain Tumor Liquid Biopsy Zhu, Lifei Cheng, Galen Ye, Dezhuang Nazeri, Arash Yue, Yimei Liu, Weijun Wang, Xiaowei Dunn, Gavin P. Petti, Allegra A. Leuthardt, Eric C. Chen, Hong Sci Rep Article Although blood-based liquid biopsies have emerged as a promising non-invasive method to detect biomarkers in various cancers, limited progress has been made for brain tumors. One major obstacle is the blood-brain barrier (BBB), which hinders efficient passage of tumor biomarkers into the peripheral circulation. The objective of this study was to determine whether FUS in combination with microbubbles can enhance the release of biomarkers from the brain tumor to the blood circulation. Two glioblastoma tumor models (U87 and GL261), developed by intracranial injection of respective enhanced green fluorescent protein (eGFP)-transduced glioblastoma cells, were treated by FUS in the presence of systemically injected microbubbles. Effect of FUS on plasma eGFP mRNA levels was determined using quantitative polymerase chain reaction. eGFP mRNA were only detectable in the FUS-treated U87 mice and undetectable in the untreated U87 mice (maximum cycle number set to 40). This finding was replicated in GL261 mice across three different acoustic pressures. The circulating levels of eGFP mRNA were 1,500–4,800 fold higher in the FUS-treated GL261 mice than that of the untreated mice for the three acoustic pressures. This study demonstrated the feasibility of FUS-enabled brain tumor liquid biopsies in two different murine glioma models across different acoustic pressures. Nature Publishing Group UK 2018-04-26 /pmc/articles/PMC5919906/ /pubmed/29700310 http://dx.doi.org/10.1038/s41598-018-24516-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhu, Lifei
Cheng, Galen
Ye, Dezhuang
Nazeri, Arash
Yue, Yimei
Liu, Weijun
Wang, Xiaowei
Dunn, Gavin P.
Petti, Allegra A.
Leuthardt, Eric C.
Chen, Hong
Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title_full Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title_fullStr Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title_full_unstemmed Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title_short Focused Ultrasound-enabled Brain Tumor Liquid Biopsy
title_sort focused ultrasound-enabled brain tumor liquid biopsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919906/
https://www.ncbi.nlm.nih.gov/pubmed/29700310
http://dx.doi.org/10.1038/s41598-018-24516-7
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