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Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging

BCAT1 (branched-chain amino acid trasaminase1) expression is necessary for the progression of IDH1 wild-type (WT) glioblastoma multiforme (GBM), which is known to be associated with aggressive tumors. The purpose of our study is to investigate the bevacizumab resistance increased by the expression o...

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Autores principales: Cho, Hye Rim, Hong, Bora, Kim, Hyeonjin, Park, Chul-Kee, Park, Sung-Hye, Park, Sunghyouk, Choi, Seung Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342501/
https://www.ncbi.nlm.nih.gov/pubmed/27626306
http://dx.doi.org/10.18632/oncotarget.11901
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author Cho, Hye Rim
Hong, Bora
Kim, Hyeonjin
Park, Chul-Kee
Park, Sung-Hye
Park, Sunghyouk
Choi, Seung Hong
author_facet Cho, Hye Rim
Hong, Bora
Kim, Hyeonjin
Park, Chul-Kee
Park, Sung-Hye
Park, Sunghyouk
Choi, Seung Hong
author_sort Cho, Hye Rim
collection PubMed
description BCAT1 (branched-chain amino acid trasaminase1) expression is necessary for the progression of IDH1 wild-type (WT) glioblastoma multiforme (GBM), which is known to be associated with aggressive tumors. The purpose of our study is to investigate the bevacizumab resistance increased by the expression of BCAT1 in IDH1 WT GBM in a rat model, which was evaluated using DSC perfusion MRI. BCAT1 sh#1 inhibits cell proliferation and limits cell migration potential in vitro. In vivo MRI showed that the increase in both tumor volume and nCBV after bevacizumab treatment in IDH1 WT tumors was significantly higher compared with BCAT1 sh#1tumors. In a histological analysis, more micro-vessel reformation by bevacizumab resistance was observed in IDH1 WT tumors than BCAT1 sh#1 tumors. These findings indicate that BCAT1 expression in IDH1 WT GBM increases resistance to bevacizumab treatment, which could be assessed by DSC perfusion MRI, and that nCBV can be a surrogate imaging biomarker for the prediction of antiangiogenic treatment in GBM.
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spelling pubmed-53425012017-03-24 Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging Cho, Hye Rim Hong, Bora Kim, Hyeonjin Park, Chul-Kee Park, Sung-Hye Park, Sunghyouk Choi, Seung Hong Oncotarget Research Paper BCAT1 (branched-chain amino acid trasaminase1) expression is necessary for the progression of IDH1 wild-type (WT) glioblastoma multiforme (GBM), which is known to be associated with aggressive tumors. The purpose of our study is to investigate the bevacizumab resistance increased by the expression of BCAT1 in IDH1 WT GBM in a rat model, which was evaluated using DSC perfusion MRI. BCAT1 sh#1 inhibits cell proliferation and limits cell migration potential in vitro. In vivo MRI showed that the increase in both tumor volume and nCBV after bevacizumab treatment in IDH1 WT tumors was significantly higher compared with BCAT1 sh#1tumors. In a histological analysis, more micro-vessel reformation by bevacizumab resistance was observed in IDH1 WT tumors than BCAT1 sh#1 tumors. These findings indicate that BCAT1 expression in IDH1 WT GBM increases resistance to bevacizumab treatment, which could be assessed by DSC perfusion MRI, and that nCBV can be a surrogate imaging biomarker for the prediction of antiangiogenic treatment in GBM. Impact Journals LLC 2016-09-08 /pmc/articles/PMC5342501/ /pubmed/27626306 http://dx.doi.org/10.18632/oncotarget.11901 Text en Copyright: © 2016 Cho et al. http://creativecommons.org/licenses/by/3.0/ 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
Cho, Hye Rim
Hong, Bora
Kim, Hyeonjin
Park, Chul-Kee
Park, Sung-Hye
Park, Sunghyouk
Choi, Seung Hong
Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title_full Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title_fullStr Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title_full_unstemmed Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title_short Assessment of bevacizumab resistance increased by expression of BCAT1 in IDH1 wild-type glioblastoma: application of DSC perfusion MR imaging
title_sort assessment of bevacizumab resistance increased by expression of bcat1 in idh1 wild-type glioblastoma: application of dsc perfusion mr imaging
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342501/
https://www.ncbi.nlm.nih.gov/pubmed/27626306
http://dx.doi.org/10.18632/oncotarget.11901
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