Suppr超能文献

在肠道肿瘤中追踪 Notch1 表达细胞的谱系揭示了一种独特的癌症干细胞群体。

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

机构信息

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.

出版信息

Sci Rep. 2019 Jan 29;9(1):888. doi: 10.1038/s41598-018-37301-3.

Abstract

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.

摘要

结肠肿瘤呈层级结构,包含多能自我更新细胞,称为癌症干细胞(CSCs)。我们之前已经表明 Notch1 受体在肠干细胞(ISCs)中表达;鉴于 Notch 信号在促进肠道肿瘤发生中的关键作用,我们研究了 Notch1 在肿瘤中的表达。通过两种肿瘤模型中的谱系追踪与转录组分析相结合,我们发现 Notch1+肿瘤细胞未分化、增殖,并具有无限自我更新和产生异质性克隆后代的能力。从分子水平上看,Notch1+肿瘤细胞的转录特征与 ISCs 高度相关,提示它们起源于正常隐窝细胞。令人惊讶的是,Notch1+表达标记了一小部分 CSCs,其 Lgr5 水平降低,Lgr5 是报告的 CSCs 标志物。肠道肿瘤内存在不同的干细胞群体,这凸显了更好地了解它们的层级结构和行为以确定正确的治疗细胞靶标的必要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验