Evidence map›Paper›PMID 32059178›Full record

ArticleJournal of neurosurgery2021

Targeting glioma-initiating cells via the tyrosine metabolic pathway.

Daisuke Yamashita, Joshua D Bernstock, Galal Elsayed, Hirokazu Sadahiro, Ahmed Mohyeldin, Gustavo Chagoya, Adeel Ilyas, James Mooney, Dagoberto Estevez-Ordonez, Shinobu Yamaguchi and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neurosurgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

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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

18 authors at 8 institutions in 4 countries.

Daisuke YamashitaDepartments of1Neurosurgery and.
Joshua D Bernstock2Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Galal ElsayedDepartments of1Neurosurgery and.
Hirokazu SadahiroDepartments of1Neurosurgery and.
Ahmed Mohyeldin4Department of Neurological Surgery, The Ohio State University, Wexner Medical Center, Columbus, Ohio.
Gustavo ChagoyaDepartments of1Neurosurgery and.
Adeel IlyasDepartments of1Neurosurgery and.
James MooneyDepartments of1Neurosurgery and.
Dagoberto Estevez-OrdonezDepartments of1Neurosurgery and.
Shinobu YamaguchiDepartments of1Neurosurgery and.
Victoria L FlanaryDepartments of1Neurosurgery and.
James R Hackney5Pathology.
Krishna P Bhat6Department of Translational Molecular Pathology and Brain Tumor Center, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Harley I Kornblum7Departments of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior.
Nicola Zamboni9Institute of Molecular Systems Biology, ETH Zurich, Zurich, Switzerland.
Sung-Hak KimDepartments of1Neurosurgery and.
E Antonio Chiocca2Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Ichiro NakanoDepartments of1Neurosurgery and.
University of Alabama at Birmingham · USHarvard University · USETH Zurich · CHIntel (United States) · USKorea Basic Science Institute · KRThe Ohio State University Wexner Medical Center · USThe University of Texas MD Anderson Cancer Center · USYamaguchi University · JP

Funding

UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Yvonne Yu-Hsuan Chen · 2017 to 2026
$25.2M
The unique roles of the GTP-binding/protein crosslinking enzyme transglutaminase-2 and signaling partners in aggressive cancersR01CA201402 · NCI · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2016 to 2024
$4.3M
Metabolism Informs Intertumoral & Intratumoral HeterogeneityR01NS087913 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NAKANO, ICHIRO, RICH, JEREMY N · 2014 to 2018
$2.0M
Novel role of compensatory proliferation in human brain tumorR01CA183991 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NAKANO, ICHIRO · 2015 to 2019
$1.6M
Targeting MELK-mediated EZH2 signaling in glioma stem cellsR01NS083767 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEE, JEONGWU, NAKANO, ICHIRO · 2013 to 2017
$1.3M
NCI NIH HHS P50 CA211015NCI NIH HHS R01 CA183991NCI NIH HHS R01 CA201402NINDS NIH HHS R01 NS083767NINDS NIH HHS R01 NS087913
6 · The paper itself

Abstract

objectiveDespite an aggressive multimodal therapeutic regimen, glioblastoma (GBM) continues to portend a grave prognosis, which is driven in part by tumor heterogeneity at both the molecular and cellular levels. Accordingly, herein the authors sought to identify metabolic differences between GBM tumor core cells and edge cells and, in so doing, elucidate novel actionable therapeutic targets centered on tumor metabolism.

methodsComprehensive metabolic analyses were performed on 20 high-grade glioma (HGG) tissues and 30 glioma-initiating cell (GIC) sphere culture models. The results of the metabolic analyses were combined with the Ivy GBM data set. Differences in tumor metabolism between GBM tumor tissue derived from within the contrast-enhancing region (i.e., tumor core) and that from the peritumoral brain lesions (i.e., tumor edge) were sought and explored. Such changes were ultimately confirmed at the protein level via immunohistochemistry.

resultsMetabolic heterogeneity in both HGG tumor tissues and GBM sphere culture models was identified, and analyses suggested that tyrosine metabolism may serve as a possible therapeutic target in GBM, particularly in the tumor core. Furthermore, activation of the enzyme tyrosine aminotransferase (TAT) within the tyrosine metabolic pathway influenced the noted therapeutic resistance of the GBM core.

conclusionsSelective inhibition of the tyrosine metabolism pathway may prove highly beneficial as an adjuvant to multimodal GBM therapies.

Indexed as

Base SequenceBrain NeoplasmsCell Line, TumorCells, CulturedChemotherapy, AdjuvantDrug Delivery SystemsGliomaHumansImmunohistochemistryMetabolic Networks and PathwaysMetabolomicsNitrogenTyrosineTyrosine TransaminaseNitrogenTyrosineTyrosine Transaminaseglioblastomaheterogeneityhigh-grade gliomametabolismnitrogen metabolismoncologytyrosine aminotransferase

Identifiers

PMID32059178
PMCPMC8447888
OpenAlexW3006493213

What OpenQuestion holds

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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.