The Hippo transducers TAZ and YAP in breast cancer: oncogenic activities and clinical implications

被引:79
|
作者
Maugeri-Sacca, Marcello [1 ,2 ]
Barba, Maddalena [1 ,2 ]
Pizzuti, Laura [1 ]
Vici, Patrizia [1 ]
Di Lauro, Luigi [1 ]
Dattilo, Rosanna [3 ]
Vitale, Ilio [2 ]
Bartucci, Monica [4 ]
Mottolese, Marcella [5 ]
De Maria, Ruggero [2 ]
机构
[1] Regina Elena Inst Canc Res, Div Med Oncol B, I-00144 Rome, Italy
[2] Regina Elena Inst Canc Res, Sci Direct, I-00144 Rome, Italy
[3] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[4] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[5] Regina Elena Inst Canc Res, Dept Pathol, I-00144 Rome, Italy
来源
关键词
YES-ASSOCIATED PROTEIN; EPITHELIAL-MESENCHYMAL TRANSITION; STEM-CELL PROPERTIES; TUMOR-SUPPRESSOR; TRANSCRIPTIONAL COACTIVATOR; PROSPECTIVE IDENTIFICATION; MOLECULAR PORTRAITS; PROMOTES APOPTOSIS; SIGNALING PATHWAY; TEAD/TEF FAMILY;
D O I
10.1017/erm.2015.12
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Hippo signalling is emerging as a tumour suppressor pathway whose function is regulated by an intricate network of intracellular and extracellular cues. Defects in the signal cascade lead to the activation of the Hippo transducers TAZ and YAP. Compelling preclinical evidence showed that TAZ/YAP are often aberrantly engaged in breast cancer (BC), where their hyperactivation culminates into a variety of tumour-promoting functions such as epithelial-to-mesenchymal transition, cancer stem cell generation and therapeutic resistance. Having acquired a more thorough understanding in the biology of TAZ/YAP, and the molecular outputs they elicit, has prompted a first wave of exploratory, clinically-focused analyses aimed at providing initial hints on the prognostic/predictive significance of their expression. In this review, we discuss oncogenic activities linked with TAZ/YAP in BC, and we propose clinical strategies for investigating their role as biomarkers in the clinical setting. Finally, we address the therapeutic potential of TAZ/YAP targeting and the modalities that, in our opinion, should be pursued in order to further study the biological and clinical consequences of their inhibition.
引用
收藏
页数:10
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