Evidence map›Paper›PMID 27626306›Full record

ArticleOncotarget2016

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

Hye Rim Cho, Bora Hong, Hyeonjin Kim, Chul-Kee Park, Sung-Hye Park, Sunghyouk Park, Seung Hong Choi

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hye Rim ChoDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.
Bora HongDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.
Hyeonjin KimDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.
Chul-Kee ParkDepartment of Neurosurgery, Seoul National University Hospital, Seoul, Korea.
Sung-Hye ParkDepartment of Pathology, Seoul National University Hospital, Seoul, Korea.
Sunghyouk ParkCollege of Pharmacy, Natural Product Research Institute, Seoul National University, Seoul, Korea.
Seung Hong ChoiDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Xenograft Model Antitumor AssaysAnimalsAntineoplastic Agents, ImmunologicalBevacizumabBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmGlioblastomaHumansIsocitrate DehydrogenaseMagnetic Resonance ImagingMaleRatsRNA InterferenceAntineoplastic Agents, ImmunologicalBCAT1 protein, humanBevacizumabIDH1 protein, humanIsocitrate DehydrogenaseTransaminasesBCAT1bevacizumabdynamic susceptibility contrast (DSC)glioblastoma

Identifiers

PMID27626306
PMCPMC5342501

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.