Pleiotropic Roles for ZEB1 in Cancer

被引:262
|
作者
Caramel, Julie [1 ,2 ]
Ligier, Maud [1 ,2 ]
Puisieux, Alain [1 ,2 ]
机构
[1] Univ Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Ctr Leon Berard,Canc Res Ctr Lyon,Equipe Labellis, Lyon, France
[2] Univ Lyon, LabEx DEVweCAN, Lyon, France
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; EMT-ACTIVATOR ZEB1; TRANSCRIPTION FACTORS; DRUG-RESISTANCE; CELL PLASTICITY; STEM-CELLS; PANCREATIC-CANCER; OVARIAN-CANCER; LUNG-CANCER; METASTASIS;
D O I
10.1158/0008-5472.CAN-17-2476
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ZEB1 is a prime element of a network of transcription factors that controls epithelial-to-mesenchymal transition (EMT), a reversible embryonic transdifferentiation program that allows partial or complete transition from an epithelial to a mesenchymal state. Aberrant expression of ZEB1 has been reported in a variety of human cancers, where it is generally believed to foster migration, invasion, and metastasis. Over the past few years, in vitro and in vivo observations have highlighted unsuspected intrinsic oncogenic functions of ZEB1 that impact tumorigenesis from its earliest stages. Located downstream of regulatory processes that integrate microenvironmental signals and directly implicated in feedback loops controlled by miRNAs, ZEB1 appears to be a central switch that determines cell fate. Its expression fosters malignant transformation through the mitigation of critical oncosuppressive pathways and through the conferment of stemness properties. ZEB1 is also a key determinant of cell plasticity, endowing cells with the capacity to withstand an aberrant mitogenic activity, with a profound impact on the genetic history of tumorigenesis, and to adapt to the multiple constraints encountered over the course of tumor development. (C) 2017 AACR.
引用
收藏
页码:30 / 35
页数:6
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