Evidence map›Paper›PMID 31149644›Full record

ArticleCommunications biology2019

Therapeutic benefit of combining calorie-restricted ketogenic diet and glutamine targeting in late-stage experimental glioblastoma.

Purna Mukherjee, Zachary M Augur, Mingyi Li, Collin Hill, Bennett Greenwood, Marek A Domin, Gramoz Kondakci, Niven R Narain, Michael A Kiebish, Roderick T Bronson and 3 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
8.6field-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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 138 citations in OpenAlex.

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  12. Does human cytomegalovirus provide a novel therapeutic target for patients with glioblastoma?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
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21 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

13 authors at 5 institutions in 3 countries.

Purna Mukherjee1Department of Biology, Boston College, Chestnut Hill, MA 02467 USA.
Zachary M Augur1Department of Biology, Boston College, Chestnut Hill, MA 02467 USA.
Mingyi Li1Department of Biology, Boston College, Chestnut Hill, MA 02467 USA.
Collin HillBERG LLC, Framingham, MA 01701 USA.
Bennett GreenwoodBERG LLC, Framingham, MA 01701 USA.
Marek A Domin3Mass Spectrometry Center, Chemistry Department, Boston College, Chestnut Hill, 02467 USA.
Gramoz KondakciBERG LLC, Framingham, MA 01701 USA.
Niven R NarainBERG LLC, Framingham, MA 01701 USA.
Michael A KiebishBERG LLC, Framingham, MA 01701 USA.
Roderick T Bronson4Rodent Pathology Core, Harvard Medical School, Boston, MA 02215 USA.
Gabriel Arismendi-Morillo5Facultad de Medicina, Instituto de Investigaciones Biológicas, Universidad del Zulia, 526 Maracaibo, Venezuela.
Christos Chinopoulos6Department of Medical Biochemistry, Semmelweis University, Budapest, 1094 Hungary.ORCID 0000-0003-0183-4149
Thomas N Seyfried1Department of Biology, Boston College, Chestnut Hill, MA 02467 USA.
Boston College · USFramingham State University · USHarvard University · USSemmelweis University · HUUniversidad del Zulia · VE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is an aggressive primary human brain tumour that has resisted effective therapy for decades. Although glucose and glutamine are the major fuels that drive GBM growth and invasion, few studies have targeted these fuels for therapeutic management. The glutamine antagonist, 6-diazo-5-oxo-L-norleucine (DON), was administered together with a calorically restricted ketogenic diet (KD-R) to treat late-stage orthotopic growth in two syngeneic GBM mouse models: VM-M3 and CT-2A. DON targets glutaminolysis, while the KD-R reduces glucose and, simultaneously, elevates neuroprotective and non-fermentable ketone bodies. The diet/drug therapeutic strategy killed tumour cells while reversing disease symptoms, and improving overall mouse survival. The therapeutic strategy also reduces edema, hemorrhage, and inflammation. Moreover, the KD-R diet facilitated DON delivery to the brain and allowed a lower dosage to achieve therapeutic effect. The findings support the importance of glucose and glutamine in driving GBM growth and provide a therapeutic strategy for non-toxic metabolic management.

Indexed as

Caloric RestrictionDiet, KetogenicAnimalsBody WeightBrainBrain NeoplasmsCell Line, TumorCell ProliferationDiazooxonorleucineDisease Models, AnimalFemaleFermentationGlioblastomaGlucoseGlutamineHumansDiazooxonorleucineGlucoseGlutamineKetone BodiesKetonesCancer metabolismCNS cancer

Identifiers

PMID31149644
PMCPMC6541653
OpenAlexW2947890843

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.