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


Journal

EMBO reports
ISSN: 1469-3178
Titre abrégé: EMBO Rep
Pays: England
ID NLM: 100963049

Informations de publication

Date de publication:
09 10 2023
Historique:
revised: 24 06 2023
received: 12 10 2022
accepted: 03 07 2023
medline: 10 10 2023
pubmed: 25 7 2023
entrez: 25 7 2023
Statut: ppublish

Résumé

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

Identifiants

pubmed: 37489735
doi: 10.15252/embr.202256279
pmc: PMC10561355
doi:

Substances chimiques

Arginine 94ZLA3W45F

Banques de données

GEO
['GSE226887']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e56279

Subventions

Organisme : Cancer Research UK
ID : A25142
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C596/A17196
Pays : United Kingdom
Organisme : Cancer Research UK
ID : A31287
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C57352/A29754
Pays : United Kingdom
Organisme : Cancer Research UK
ID : A23982
Pays : United Kingdom

Informations de copyright

© 2023 The Authors. Published under the terms of the CC BY 4.0 license.

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Auteurs

Kevin M Rattigan (KM)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Martha M Zarou (MM)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Zuzana Brabcova (Z)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Bodhayan Prasad (B)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Désirée Zerbst (D)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Daniele Sarnello (D)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Eric R Kalkman (ER)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Angela Ianniciello (A)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Mary T Scott (MT)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Karen Dunn (K)

Paul O'Gorman Leukaemia Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Engy Shokry (E)

Cancer Research UK Beatson Institute, Glasgow, UK.

David Sumpton (D)

Cancer Research UK Beatson Institute, Glasgow, UK.

Mhairi Copland (M)

Paul O'Gorman Leukaemia Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

Saverio Tardito (S)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.
Cancer Research UK Beatson Institute, Glasgow, UK.

Johan Vande Voorde (J)

Cancer Research UK Beatson Institute, Glasgow, UK.

Francis Mussai (F)

Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

Paul Cheng (P)

Bio-cancer Treatment International Ltd, Hong Kong Science Park, Shatin, New Territories, Hong Kong.

G Vignir Helgason (GV)

Wolfson Wohl Cancer Research Centre, School of Cancer Sciences, University of Glasgow, Glasgow, UK.

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