Evidence map›Paper›PMID 32312953›Full record

ArticleCell death & disease2020

Enhanced fatty acid oxidation provides glioblastoma cells metabolic plasticity to accommodate to its dynamic nutrient microenvironment.

Shiva Kant, Pravin Kesarwani, Antony Prabhu, Stewart F Graham, Katie L Buelow, Ichiro Nakano, Prakash Chinnaiyan

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
6.0field-weighted citation impact, top 2% 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

98 citing papers in PubMed, 140 citations in OpenAlex.

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  16. Integrating Metabolic Modulation and Nanomedicine for Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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38 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Shiva KantDepartment of Radiation Oncology, Beaumont Health, Royal Oak, MI, USA.
Pravin KesarwaniDepartment of Radiation Oncology, Beaumont Health, Royal Oak, MI, USA.
Antony PrabhuDepartment of Radiation Oncology, Beaumont Health, Royal Oak, MI, USA.
Stewart F GrahamDepartment of Metabolomics and Obstetrics/Gynecology, Beaumont Research Institute, Beaumont Health, Royal Oak, MI, USA.
Katie L BuelowDepartment of Radiation Oncology, Beaumont Health, Royal Oak, MI, USA.
Ichiro NakanoDepartment of Neurosurgery, University of Alabama at Birmingham, Alabama, USA.
Prakash ChinnaiyanDepartment of Radiation Oncology, Beaumont Health, Royal Oak, MI, USA. Prakash.Chinnaiyan@beaumont.edu.
Beaumont Health · USOakland University · USUniversity of Alabama at Birmingham · US

Funding

Developing therapeutic strategies to elicit metabolic synthetic lethality in glioblastomaR01NS110838 · NINDS · WILLIAM BEAUMONT HOSPITAL RESEARCH INST · PI CHINNAIYAN, PRAKASH · 2020 to 2024
$1.7M
Biologic consequence and therapeuticimplications of cysteine catabolism in glioblastomaR21NS090087 · NINDS · WILLIAM BEAUMONT HOSPITAL RESEARCH INST · PI CHINNAIYAN, PRAKASH · 2016 to 2017
$418k
NINDS NIH HHS R01 NS110838NINDS NIH HHS R21 NS090087
6 · The paper itself

Abstract

Despite advances in molecularly characterizing glioblastoma (GBM), metabolic alterations driving its aggressive phenotype are only beginning to be recognized. Integrative cross-platform analysis coupling global metabolomic and gene expression profiling on patient-derived glioma identified fatty acid β-oxidation (FAO) as a metabolic node in GBM. We determined that the biologic consequence of enhanced FAO is directly dependent upon tumor microenvironment. FAO serves as a metabolic cue to drive proliferation in a β-HB/GPR109A dependent autocrine manner in nutrient favorable conditions, while providing an efficient, alternate source of ATP only in nutrient unfavorable conditions. Rational combinatorial strategies designed to target these dynamic roles FAO plays in gliomagenesis resulted in necroptosis-mediated metabolic synthetic lethality in GBM. In summary, we identified FAO as a dominant metabolic node in GBM that provides metabolic plasticity, allowing these cells to adapt to their dynamic microenvironment. Combinatorial strategies designed to target these diverse roles FAO plays in gliomagenesis offers therapeutic potential in GBM.

Indexed as

Brain NeoplasmsCell Line, TumorCell PlasticityFatty AcidsGene Expression ProfilingGlioblastomaHumansMetabolomicsOxidation-ReductionPhenotypeTumor MicroenvironmentFatty Acids

Identifiers

PMID32312953
PMCPMC7170895
OpenAlexW3017111557

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.