Evidence map›Paper›PMID 37489735›Full record

ArticleEMBO reports2023

Arginine dependency is a therapeutically exploitable vulnerability in chronic myeloid leukaemic stem cells.

Kevin M Rattigan, Martha M Zarou, Zuzana Brabcova, Bodhayan Prasad, Désirée Zerbst, Daniele Sarnello, Eric R Kalkman, Angela Ianniciello, Mary T Scott, Karen Dunn and 8 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

18 authors at 4 institutions in 3 countries.

Kevin M RattiganWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-0212-0017
Martha M ZarouWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-0152-1599
Zuzana BrabcovaWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Bodhayan PrasadWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0002-7383-2460
Désirée ZerbstWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Daniele SarnelloWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-4193-2464
Eric R KalkmanWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0002-1108-6589
Angela IannicielloWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-1886-6614
Mary T ScottWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Karen DunnPaul O'Gorman Leukaemia Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Engy ShokryCancer Research UK Beatson Institute, Glasgow, UK.
David SumptonCancer Research UK Beatson Institute, Glasgow, UK.ORCID 0000-0002-9004-4079
Mhairi CoplandPaul O'Gorman Leukaemia Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Saverio TarditoWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0002-5294-8683
Johan Vande VoordeCancer Research UK Beatson Institute, Glasgow, UK.
Francis MussaiInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0003-3342-0047
Paul ChengBio-cancer Treatment International Ltd, Hong Kong Science Park, Shatin, New Territories, Hong Kong.
G Vignir HelgasonWolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.ORCID 0000-0003-1616-132X
University of Glasgow · GBCancer Research UK Scotland Institute · GBHong Kong Science and Technology Parks Corporation · HKUniversity of Birmingham · GB

Funding

Cancer Research UK 29754Cancer Research UK A23982Cancer Research UK A25142Cancer Research UK A31287Cancer Research UK C57352/A29754Cancer Research UK C596/A17196
6 · The paper itself

Abstract

To fuel accelerated proliferation, leukaemic cells undergo metabolic deregulation, which can result in specific nutrient dependencies. Here, we perform an amino acid drop-out screen and apply pre-clinical models of chronic phase chronic myeloid leukaemia (CML) to identify arginine as a nutrient essential for primary human CML cells. Analysis of the Microarray Innovations in Leukaemia (MILE) dataset uncovers reduced ASS1 levels in CML compared to most other leukaemia types. Stable isotope tracing reveals repressed activity of all urea cycle enzymes in patient-derived CML CD34

Indexed as

ArginineLeukemia, Myelogenous, Chronic, BCR-ABL PositiveApoptosisHumansNeoplastic Stem CellsStem CellsArginineamino acidsleukaemic stem cellsmetabolismtherapy resistance

Identifiers

PMID37489735
PMCPMC10561355
OpenAlexW4385230698

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.