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

被引:12
作者
Mourao, Larissa [1 ,2 ,3 ,4 ]
Jacquemin, Guillaume [1 ,2 ]
Huyghe, Mathilde [1 ]
Nawrocki, Wojciech J. [5 ]
Menssouri, Naoual [1 ,6 ]
Servant, Nicolas [6 ,7 ]
Fre, Silvia [1 ]
机构
[1] PSL Res Univ, Inst Curie, CNRS, INSERM,U934,UMR3215, F-75248 Paris 05, France
[2] UPMC Univ Paris VI, Sorbonne Univ, F-75005 Paris, France
[3] Univ Amsterdam, Sect Mol Cytol, Amsterdam, Netherlands
[4] Univ Amsterdam, Van Leeuwenhoek Ctr Adv Microscopy, Swammerdam Inst Life Sci, Amsterdam, Netherlands
[5] Vrije Univ Amsterdam, Dept Phys & Astron, De Boelelaan 1081, NL-1081 HV Amsterdam, Netherlands
[6] PSL Res Univ, Inst Curie, INSERM, U900, F-75005 Paris, France
[7] PSL Res Univ, Mines ParisTech, CBIO Ctr Computat Biol, F-75006 Paris, France
基金
欧洲研究理事会;
关键词
MARKER; NOTCH; EXPRESSION; COLON; GENE; BMI1; DIFFERENTIATION; IDENTIFICATION; PROLIFERATION; TUMORIGENESIS;
D O I
10.1038/s41598-018-37301-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:14
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