Evidence map›Paper›PMID 35782058›Full record

ArticleBioMed research international2022

Characterisation of Expression the Arginine Pathway Enzymes in Childhood Brain Tumours to Determine Susceptibility to Therapeutic Arginine Depletion.

Eleanor Bishop, Monika Dimitrova, Alexander Froggatt, Maria Estevez-Cebrero, Lisa C D Storer, Francis Mussai, Simon Paine, Richard G Grundy, Madhumita Dandapani

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 6 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 3 institutions in 1 country.

Eleanor BishopChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.
Monika DimitrovaChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.
Alexander FroggattChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.
Maria Estevez-CebreroChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.ORCID https://orcid.org/0000-0002-6703-8869
Lisa C D StorerChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.
Francis MussaiInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID https://orcid.org/0000-0003-3342-0047
Simon PaineNottingham University Hospitals NHS Trust, Nottingham, UK.ORCID https://orcid.org/0000-0002-1434-3931
Richard G GrundyChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.ORCID https://orcid.org/0000-0002-2585-2539
Madhumita DandapaniChildrens Brain Tumour Research Centre, School of Medicine, University of Nottingham, UK.ORCID https://orcid.org/0000-0001-8444-6007
University of Nottingham · GBNottingham University Hospitals NHS Trust · GBUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite significant improvements in treatment and survival in paediatric cancers, outcomes for children with brain tumours remain poor. Novel therapeutic approaches are needed to improve survival and quality of survival. Extracellular arginine dependency (auxotrophy) has been recognised in several tumours as a potential therapeutic target. This dependency is due to the inability of cancer cells to recycle or synthesise intracellular arginine through the urea cycle pathway compared to normal cells. Whilst adult glioblastoma exhibits this dependency, the expression of the arginine pathway enzymes has not been delineated in paediatric brain tumours. We used immunohistochemical (IHC) methods to stain for arginine pathway enzymes in paediatric high-grade glioma (pHGG), low-grade glioma (pLGG), ependymoma (EPN), and medulloblastoma (MB) tumour tissue microarrays (TMAs). The antibodies detected protein expression of the metaboliser arginase (Arg1 and Arg2); recycling enzymes ornithine transcarbamoylase (OTC), argininosuccinate synthetase (ASS1), and argininosuccinate lyase (ASL); and the transporter SLC7A1. Deficiency of OTC, ASS1, and ASL was seen in 87.5%, 94%, and 79% of pHGG samples, respectively, consistent with an auxotrophic signature. Similar result was obtained in pLGG with 96%, 93%, and 91% of tumours being deficient in ASL, ASS1, and OTC, respectively. 79%, 88%, and 85% of MB cases were ASL, ASS1, and OTC deficient whilst ASL and OTC were deficient in 57% and 91% of EPN samples. All tumour types highly expressed SLC7A1 and Arginase, with Arg2 being the main isoform, demonstrating that they could transport and utilise arginine. Our results show that pHGG, pLGG, EPN, and MB demonstrate arginine auxotrophy based on protein expression and are likely to be susceptible to arginine depletion. Pegylated arginase (BCT-100) is currently in phase I/II trials in relapsed pHGG. Our results suggest that therapeutic arginine depletion may also be useful in other tumour types and IHC analysis of patient tumour samples could help identify patients likely to benefit from this treatment.

Indexed as

Brain NeoplasmsCerebellar NeoplasmsGliomaMedulloblastomaAdultArginaseArginineArgininosuccinate LyaseChildEpendymomaHumansOrnithine CarbamoyltransferaseArginaseArginineArgininosuccinate LyaseOrnithine Carbamoyltransferase

Identifiers

PMID35782058
PMCPMC9242779
OpenAlexW4283327641

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.