Evidence map›Paper›PMID 29142297›Full record

ArticleScientific reports2017

5-Aminolevulinic Acid Guided Sampling of Glioblastoma Microenvironments Identifies Pro-Survival Signaling at Infiltrative Margins.

James L Ross, Lee A D Cooper, Jun Kong, David Gutman, Merete Williams, Carol Tucker-Burden, Myles R McCrary, Alexandros Bouras, Milota Kaluzova, William D Dunn and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Tumour immune landscape of paediatric high-grade gliomas.Brain : a journal of neurology · 2021
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
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

13 authors.

James L RossDepartments of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, Georgia.
Lee A D CooperBiomedical Informatics, Emory University, Atlanta, GA 30322, Georgia.ORCID 0000-0002-3504-4965
Jun KongBiomedical Informatics, Emory University, Atlanta, GA 30322, Georgia.
David GutmanNeurology, Emory University, Atlanta, GA 30322, Georgia.
Merete WilliamsDepartments of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, Georgia.
Carol Tucker-BurdenDepartments of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, Georgia.
Myles R McCraryEmory University School of Medicine, Emory University, Atlanta, GA 30322, Georgia.
Alexandros BourasDepartment of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY, 10003, USA.
Milota KaluzovaPediatrics, Emory University, Atlanta, GA 30322, Georgia.
William D DunnBiomedical Informatics, Emory University, Atlanta, GA 30322, Georgia.
Duc DuongNeurology, Emory University, Atlanta, GA 30322, Georgia.
Constantinos G HadjipanayisDepartment of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY, 10003, USA. Constantinos.Hadjipanayis@mountsinai.org.
Daniel J BratDepartments of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, Georgia. dbrat@emory.edu.

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
Advanced Development of an Open-source Platform for Web-based Integrative Digital Image Analysis in CancerU24CA194362 · NCI · EMORY UNIVERSITY · PI COOPER, LEE, GUTMAN, DAVID ANDREW · 2015 to 2019
$3.6M
Molecular Target Variation Across Environments and at Margins of GlioblastomaR01CA176659 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BRAT, DANIEL J, HADJIPANAYIS, CONSTANTINOS GEORGE · 2013 to 2017
$2.3M
Quantitative Analysis of GBM Invasion Mechanisms with New Imaging ProtocolK25CA181503 · NCI · GEORGIA STATE UNIVERSITY · PI KONG, JUN · 2014 to 2018
$592k
Multiscale Framework for Molecular Heterogeneity AnalysisK22LM011576 · NLM · EMORY UNIVERSITY · PI COOPER, LEE · 2013 to 2015
$485k
NCI NIH HHS K25 CA181503NCI NIH HHS P30 CA138292NCI NIH HHS R01 CA176659NCI NIH HHS U24 CA194362NIGMS NIH HHS T32 GM008169NLM NIH HHS K22 LM011576
6 · The paper itself

Abstract

Glioblastoma (GBM) contains diverse microenvironments with uneven distributions of oncogenic alterations and signaling networks. The diffusely infiltrative properties of GBM result in residual tumor at neurosurgical resection margins, representing the source of relapse in nearly all cases and suggesting that therapeutic efforts should be focused there. To identify signaling networks and potential druggable targets across tumor microenvironments (TMEs), we utilized 5-ALA fluorescence-guided neurosurgical resection and sampling, followed by proteomic analysis of specific TMEs. Reverse phase protein array (RPPA) was performed on 205 proteins isolated from the tumor margin, tumor bulk, and perinecrotic regions of 13 previously untreated, clinically-annotated and genetically-defined high grade gliomas. Differential protein and pathway signatures were established and then validated using western blotting, immunohistochemistry, and comparable TCGA RPPA datasets. We identified 37 proteins differentially expressed across high-grade glioma TMEs. We demonstrate that tumor margins were characterized by pro-survival and anti-apoptotic proteins, whereas perinecrotic regions were enriched for pro-coagulant and DNA damage response proteins. In both our patient cohort and TCGA cases, the data suggest that TMEs possess distinct protein expression profiles that are biologically and therapeutically relevant.

Indexed as

ProteomicsAdultAgedAminolevulinic AcidErbB ReceptorsFemaleFluorescenceGlioblastomaHumansMaleMargins of ExcisionMiddle AgedNeoplasm Recurrence, LocalNeoplasm, ResidualProtein Array AnalysisPTEN PhosphohydrolaseAminolevulinic AcidEGFR protein, humanErbB ReceptorsPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID29142297
PMCPMC5688093

What OpenQuestion holds

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LicenceCC BY
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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.