Evidence map›Paper›PMID 33500708›Full record

ReviewTheranostics2021

Beyond glucose: alternative sources of energy in glioblastoma.

John L Caniglia, Anvesh Jalasutram, Swapna Asuthkar, Joseph Sahagun, Simon Park, Aditya Ravindra, Andrew J Tsung, Maheedhara R Guda, Kiran K Velpula

Open access · goldAbstract readReview
In one paragraph

Review in Theranostics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

47 citing papers in PubMed, 52 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

9 authors at 1 institution in 1 country.

John L CanigliaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Anvesh JalasutramDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Swapna AsuthkarDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Joseph SahagunDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Simon ParkDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Aditya RavindraDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Andrew J TsungDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Maheedhara R GudaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Kiran K VelpulaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria.
Illinois College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common malignant brain tumor in adults. With a designation of WHO Grade IV, it is also the most lethal primary brain tumor with a median survival of just 15 months. This is often despite aggressive treatment that includes surgical resection, radiation therapy, and chemotherapy. Based on the poor outcomes and prevalence of the tumor, the demand for innovative therapies continues to represent a pressing issue for clinicians and researchers. In terms of therapies targeting metabolism, the prevalence of the Warburg effect has led to a focus on targeting glucose metabolism to halt tumor progression. While glucose is the dominant source of growth substrate in GBM, a number of unique metabolic pathways are exploited in GBM to meet the increased demand for replication and progression. In this review we aim to explore how metabolites from fatty acid oxidation, the urea cycle, the glutamate-glutamine cycle, and one-carbon metabolism are shunted toward energy producing pathways to meet the high energy demand in GBM. We will also explore how the process of autophagy provides a reservoir of nutrients to support viable tumor cells. By so doing, we aim to establish a foundation of implicated metabolic mechanisms supporting growth and tumorigenesis of GBM within the literature. With the sparse number of therapeutic interventions specifically targeting metabolic pathways in GBM, we hope that this review expands further insight into the development of novel treatment modalities.

Indexed as

Energy MetabolismAnimalsBrain NeoplasmsGlioblastomaGlucoseHumansGlucosearginineautophagyfatty acidsglioblastomaglutaminemetabolism

Identifiers

PMID33500708
PMCPMC7797684
OpenAlexW3112208293

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.