Phenotypic plasticity and epithelial-mesenchymal transitions in cancer and normal stem cells?

被引:176
作者
Scheel, Christina [1 ]
Weinberg, Robert A. [1 ,2 ,3 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA USA
[3] MIT, Ludwig Ctr Mol Oncol, Cambridge, MA 02139 USA
关键词
cancer stem cells; stem cells; tumor-initiating ability; self-renewal; epithelial-mesenchymal transition; multi-step progression; cellular state; phenotypic plasticity; MELANOMA-CELLS; IDENTIFICATION; HETEROGENEITY; STATE; EMT;
D O I
10.1002/ijc.26311
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer stem cells (CSCs) are similar to normal stem cells in their ability to self-renew and to generate large populations of more differentiated descendants. In contrast to the hierarchical organization that is presumed to be the prevalent mode of normal tissue homeostasis, phenotypic plasticity allows cancer cells to dynamically enter into and exit from stem-cell states. The epithelial-mesenchymal transition (EMT) has been closely associated with the acquisition of both invasive and stem-cell properties in cancer cells. Thereby, EMT programs emerge as important regulators of phenotypic plasticity in cancer cells including their entrance into stem-cell states. Much is still to be learned about the regulation of EMTs through epigenetic mechanisms in cancer cells and the contributions that EMT programs make to normal tissue homeostasis.
引用
收藏
页码:2310 / 2314
页数:5
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