Evidence map›Paper›PMID 23793099›Full record

ArticleNature medicine2013

BCAT1 promotes cell proliferation through amino acid catabolism in gliomas carrying wild-type IDH1.

Martje Tönjes, Sebastian Barbus, Yoon Jung Park, Wei Wang, Magdalena Schlotter, Anders M Lindroth, Sabrina V Pleier, Alfa H C Bai, Daniela Karra, Rosario M Piro and 24 more

Abstract read
In one paragraph

Article in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 322 papers.

0numbers the graph read from it
0cells of the map it votes in
322citing papers in PubMed
12.1field-weighted citation impact, top 1% of its field
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

322 citing papers in PubMed, 471 citations in OpenAlex.

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  17. Integrating Spatial Proteogenomics in Cancer Research.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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262 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors at 9 institutions in 2 countries.

Martje Tönjes *Division of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Sebastian Barbus *Division of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Yoon Jung ParkDivision of Epigenomics and Cancer Risk Factors, DKFZ, Heidelberg, Germany.
Wei WangDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Magdalena SchlotterDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Anders M LindrothDivision of Epigenomics and Cancer Risk Factors, DKFZ, Heidelberg, Germany.
Sabrina V PleierDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Alfa H C BaiDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Daniela KarraDepartment of Neuropathology, Heinrich Heine University, Düsseldorf, Germany.
Rosario M PiroDepartment of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology and Bioquant, University of Heidelberg, Heidelberg, Germany.
Jörg FelsbergDepartment of Neuropathology, Heinrich Heine University, Düsseldorf, Germany.
Adele AddingtonDepartment of Human Nutrition, Foods and Exercise, Virginia Polytechnic Institute, Blacksburg, Virginia, USA.
Dieter LemkeClinical Cooperation Unit Neurooncology, DKFZ, Heidelberg, Germany.
Irene WeibrechtDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Volker HovestadtDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Claudio G RolliDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems, Stuttgart, Germany.
Benito CamposDivision of Experimental Neurosurgery, University of Heidelberg, Heidelberg, Germany.
Sevin TurcanHuman Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Dominik SturmDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Hendrik WittDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Timothy A ChanHuman Oncology and Pathogenesis Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Christel Herold-MendeDivision of Experimental Neurosurgery, University of Heidelberg, Heidelberg, Germany.
Ralf KemkemerDepartment of New Materials and Biosystems, Max Planck Institute for Intelligent Systems, Stuttgart, Germany.
Rainer KönigDepartment of Bioinformatics and Functional Genomics, Institute of Pharmacy and Molecular Biotechnology and Bioquant, University of Heidelberg, Heidelberg, Germany.
Kathrin SchmidtDepartment of General Pediatrics, Division of Inborn Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
William-Edmund HullCore Facility, Molecular Structural Analysis, DKFZ, Heidelberg, Germany.
Stefan M PfisterDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Manfred JugoldCore Facility, Small Animal Imaging Center, DKFZ, Heidelberg, Germany.
Susan M HutsonDepartment of Human Nutrition, Foods and Exercise, Virginia Polytechnic Institute, Blacksburg, Virginia, USA.
Christoph PlassDivision of Epigenomics and Cancer Risk Factors, DKFZ, Heidelberg, Germany.
Jürgen G OkunDepartment of General Pediatrics, Division of Inborn Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.
Guido ReifenbergerDepartment of Neuropathology, Heinrich Heine University, Düsseldorf, Germany.
Peter LichterDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Bernhard RadlwimmerDivision of Molecular Genetics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Heidelberg University · DEDKFZ-ZMBH Alliance · DEHeinrich Heine University Düsseldorf · DEEpigenomics (Germany) · DEGerman Cancer Research Center · DEMax Planck Institute for Intelligent Systems · DEMemorial Sloan Kettering Cancer Center · USUniversity Hospital Heidelberg · DEVirginia Tech · US

Funding

Translational Research in Oncology Training ProgramT32CA160001 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2011 to 2020
$2.0M
NCI NIH HHS T32 CA160001
6 · The paper itself

Abstract

Here we show that glioblastoma express high levels of branched-chain amino acid transaminase 1 (BCAT1), the enzyme that initiates the catabolism of branched-chain amino acids (BCAAs). Expression of BCAT1 was exclusive to tumors carrying wild-type isocitrate dehydrogenase 1 (IDH1) and IDH2 genes and was highly correlated with methylation patterns in the BCAT1 promoter region. BCAT1 expression was dependent on the concentration of α-ketoglutarate substrate in glioma cell lines and could be suppressed by ectopic overexpression of mutant IDH1 in immortalized human astrocytes, providing a link between IDH1 function and BCAT1 expression. Suppression of BCAT1 in glioma cell lines blocked the excretion of glutamate and led to reduced proliferation and invasiveness in vitro, as well as significant decreases in tumor growth in a glioblastoma xenograft model. These findings suggest a central role for BCAT1 in glioma pathogenesis, making BCAT1 and BCAA metabolism attractive targets for the development of targeted therapeutic approaches to treat patients with glioblastoma.

Indexed as

Cell ProliferationAmino Acids, Branched-ChainAnimalsBrain NeoplasmsCell Line, TumorFemaleGliomaHEK293 CellsHumansIsocitrate DehydrogenaseMetabolismMiceMice, NudeModels, BiologicalTransaminasesAmino Acids, Branched-ChainBCAT1 protein, humanIDH1 protein, humanIsocitrate DehydrogenaseTransaminases

Identifiers

PMID23793099
PMCPMC4916649
OpenAlexW2074983857

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.