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BCAT1 is a New MR Imaging-related Biomarker for Prognosis Prediction in IDH1-wildtype Glioblastoma Patients

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dc.contributor.authorHye Rim Cho-
dc.contributor.authorHyejin Jeon-
dc.contributor.authorChul-Kee Park-
dc.contributor.authorSung-Hye Park-
dc.contributor.authorKoung Mi Kang-
dc.contributor.authorSeung Hong Choi-
dc.date.accessioned2018-02-02T06:42:54Z-
dc.date.available2018-02-02T06:42:54Z-
dc.date.created2018-01-23-
dc.date.issued2017-12-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/4330-
dc.description.abstractIsocitrate dehydrogenase 1 (IDH1)-wildtype glioblastoma (GBM) has found to be accompanied with increased expression of branched-chain amino acid trasaminase1 (BCAT1), which is associated with tumor growth and disease progression. In this retrospective study, quantitative RT-PCR, immunohistochemistry, and western blot were performed with GBM patient tissues to evaluate the BCAT1 level. Quantitative MR imaging parameters were evaluated from DSC perfusion imaging, DWI, contrast-enhanced T1WI and FLAIR imaging using a 3T MR scanner. The level of BCAT1 was significantly higher in IDH1-wildtype patients than in IDH1-mutant patients obtained in immunohistochemistry and western blot. The BCAT1 level was significantly correlated with the mean and 95th percentile-normalized CBV as well as the mean ADC based on FLAIR images. In addition, the 95th percentile-normalized CBV from CE T1WI also had a significant correlation with the BCAT1 level. Moreover, the median PFS in patients with BCAT1 expression <100 was longer than in those with BCAT1 expression ≥100. Taken together, we found that a high BCAT1 level is correlated with high CBV and a low ADC value as well as the poor prognosis of BCAT1 expression is related to the aggressive nature of GBM. © 2017 The Author(s)-
dc.description.uri1-
dc.language영어-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleBCAT1 is a New MR Imaging-related Biomarker for Prognosis Prediction in IDH1-wildtype Glioblastoma Patients-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000418323900052-
dc.identifier.scopusid2-s2.0-85038600452-
dc.identifier.rimsid62051-
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorHye Rim Cho-
dc.contributor.affiliatedAuthorHyejin Jeon-
dc.contributor.affiliatedAuthorSeung Hong Choi-
dc.identifier.doi10.1038/s41598-017-17062-1-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.7, no.1, pp.17740-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume7-
dc.citation.number1-
dc.citation.startPage17740-
dc.date.scptcdate2018-10-01-
dc.description.scptc1-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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Center for Nanoparticle Research(나노입자 연구단) > 1. Journal Papers (저널논문)
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