EMT in breast cancer stem cell generation

被引：56

作者：

Ansieau, Stephane ^{[1
,2
,3
,4
,5
]}

机构：

[1] INSERM, UMR 1052, F-69008 Lyon, France

[2] CNRS, UMR 5286, Lyon, France

[3] Univ Lyon, UMR S 1052, Lyon, France

[4] Ctr Leon Berard, F-69373 Lyon, France

[5] LabEx DEVweCAN, F-69008 Lyon, France

来源：

CANCER LETTERS | 2013年 / 338卷 / 01期

关键词：

Cancer stem cells; Epithelial-to-mesenchymal transition; Cell plasticity; Embryonic EMT-inducers; Breast; EPITHELIAL-MESENCHYMAL TRANSITION; GENE-EXPRESSION SIGNATURE; CLAUDIN-LOW; TUMOR PROGRESSION; COLON-CANCER; K-RAS; TWIST; P53; PROGENITORS; PHENOTYPE;

D O I：

10.1016/j.canlet.2012.05.014

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 [肿瘤学];

摘要：

The concept of cancer stem cells (CSCs) has been proposed to explain the ability of single disseminated cancer cells to reconstitute tumours with heterogeneity similar to that of the primary tumour they arise from. Although this concept is now commonly accepted, the origin of these CSCs remains a source of debate. First proposed to arise through stem/progenitor cell transformation, CSCs might also or alternatively arise from differentiated cancer cells through epithelial to mesenchymal transition (EMT), an embryonic transdifferentiation process. Using breast carcinomas as a study model, I propose revisiting the role of EMT in generating CSCs and the debate on potential underlying mechanisms and biological significance. (C) 2012 Published by Elsevier Ireland Ltd.

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页码：63 / 68

页数：6

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