CD93 is expressed on chronic myeloid leukemia stem cells and identifies a quiescent population which persists after tyrosine kinase inhibitor therapy.


Journal

Leukemia
ISSN: 1476-5551
Titre abrégé: Leukemia
Pays: England
ID NLM: 8704895

Informations de publication

Date de publication:
06 2020
Historique:
received: 08 07 2019
accepted: 05 12 2019
revised: 17 11 2019
pubmed: 4 1 2020
medline: 8 10 2020
entrez: 4 1 2020
Statut: ppublish

Résumé

The introduction of BCR-ABL tyrosine kinase inhibitors has revolutionized the treatment of chronic myeloid leukemia (CML). A major clinical aim remains the identification and elimination of low-level disease persistence, termed "minimal residual disease". The phenomenon of disease persistence suggests that despite targeted therapeutic approaches, BCR-ABL-independent mechanisms exist which sustain the survival of leukemic stem cells (LSCs). Although other markers of a primitive CML LSC population have been identified in the preclinical setting, only CD26 appears to offer clinical utility. Here we demonstrate consistent and selective expression of CD93 on a lin

Identifiants

pubmed: 31896780
doi: 10.1038/s41375-019-0684-5
pii: 10.1038/s41375-019-0684-5
pmc: PMC7272220
mid: EMS85133
doi:

Substances chimiques

Biomarkers, Tumor 0
Membrane Glycoproteins 0
Protein Kinase Inhibitors 0
Receptors, Complement 0
complement 1q receptor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1613-1625

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 100626
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : CAF/08/09
Pays : United Kingdom
Organisme : Cancer Research UK
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Références

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Auteurs

Ross Kinstrie (R)

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

Gillian A Horne (GA)

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

Heather Morrison (H)

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

David Irvine (D)

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

Chinmay Munje (C)

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

Eduardo Gómez Castañeda (EG)

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

Hothri A Moka (HA)

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

Karen Dunn (K)

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

Jennifer E Cassels (JE)

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

Narissa Parry (N)

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

Cassie J Clarke (CJ)

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

Mary T Scott (MT)

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

Richard E Clark (RE)

Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.

Tessa L Holyoake (TL)

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

Helen Wheadon (H)

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

Mhairi Copland (M)

Paul O'Gorman Leukaemia Research Centre, Institute of Cancer Sciences, University of Glasgow, Glasgow, UK. Mhairi.Copland@glasgow.ac.uk.

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