Lineage tracing of Notch1-expressing cells in intestinal tumours reveals a distinct population of cancer stem cells.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
29 01 2019
Historique:
received: 08 06 2018
accepted: 04 12 2018
entrez: 31 1 2019
pubmed: 31 1 2019
medline: 29 8 2020
Statut: epublish

Résumé

Colon tumours are hierarchically organized and contain multipotent self-renewing cells, called Cancer Stem Cells (CSCs). We have previously shown that the Notch1 receptor is expressed in Intestinal Stem Cells (ISCs); given the critical role played by Notch signalling in promoting intestinal tumourigenesis, we explored Notch1 expression in tumours. Combining lineage tracing in two tumour models with transcriptomic analyses, we found that Notch1+ tumour cells are undifferentiated, proliferative and capable of indefinite self-renewal and of generating a heterogeneous clonal progeny. Molecularly, the transcriptional signature of Notch1+ tumour cells highly correlates with ISCs, suggestive of their origin from normal crypt cells. Surprisingly, Notch1+ expression labels a subset of CSCs that shows reduced levels of Lgr5, a reported CSCs marker. The existence of distinct stem cell populations within intestinal tumours highlights the necessity of better understanding their hierarchy and behaviour, to identify the correct cellular targets for therapy.

Identifiants

pubmed: 30696875
doi: 10.1038/s41598-018-37301-3
pii: 10.1038/s41598-018-37301-3
pmc: PMC6351556
doi:

Substances chimiques

Biomarkers 0
LGR5 protein, human 0
NOTCH1 protein, human 0
Receptor, Notch1 0
Receptors, G-Protein-Coupled 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

888

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Auteurs

Larissa Mourao (L)

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248, Paris, Cedex 05, France.
Sorbonne University, UPMC University of Paris VI, F-75005, Paris, France.
Section of Molecular Cytology and Van Leeuwenhoek Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.

Guillaume Jacquemin (G)

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248, Paris, Cedex 05, France.
Sorbonne University, UPMC University of Paris VI, F-75005, Paris, France.

Mathilde Huyghe (M)

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248, Paris, Cedex 05, France.

Wojciech J Nawrocki (WJ)

Vrije Universiteit Amsterdam, Department of Physics and Astronomy, De Boelelaan 1081, 1081HV, Amsterdam, The Netherlands.

Naoual Menssouri (N)

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248, Paris, Cedex 05, France.
Institut Curie, PSL Research University, INSERM U900, 75005, Paris, France.

Nicolas Servant (N)

Institut Curie, PSL Research University, INSERM U900, 75005, Paris, France.
Mines ParisTech, PSL Research University, CBIO-Centre for Computational Biology, 75006, Paris, France.

Silvia Fre (S)

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248, Paris, Cedex 05, France. silvia.fre@curie.fr.

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