Mechanisms of Hippo pathway regulation

被引:1327
作者
Meng, Zhipeng [1 ]
Moroishi, Toshiro [1 ]
Guan, Kun-Liang [1 ]
机构
[1] Univ Calif San Diego, Moores Canc Ctr, Dept Pharmacol, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
LATS; MAP4K; MST; TAZ; TEAD; YAP; TUMOR-SUPPRESSOR PATHWAY; PHOSPHORYLATION-DEPENDENT MANNER; PROTEIN-INTERACTION NETWORK; AMPK-MEDIATED REGULATION; GENOME-WIDE ASSOCIATION; CELL-CYCLE EXIT; SIGNALING-PATHWAY; CONTACT INHIBITION; TISSUE-GROWTH; YAP PATHWAY;
D O I
10.1101/gad.274027.115
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Hippo pathway was initially identified in Drosophila melanogaster screens for tissue growth two decades ago and has been a subject extensively studied in both Drosophila and mammals in the last several years. The core of the Hippo pathway consists of a kinase cascade, transcription coactivators, and DNA-binding partners. Recent studies have expanded the Hippo pathway as a complex signaling network with >30 components. This pathway is regulated by intrinsic cell machineries, such as cell-cell contact, cell polarity, and actin cytoskeleton, as well as a wide range of signals, including cellular energy status, mechanical cues, and hormonal signals that act through G-protein-coupled receptors. The major functions of the Hippo pathway have been defined to restrict tissue growth in adults and modulate cell proliferation, differentiation, and migration in developing organs. Furthermore, dysregulation of the Hippo pathway leads to aberrant cell growth and neoplasia. In this review, we focus on recent developments in our understanding of the molecular actions of the core Hippo kinase cascade and discuss key open questions in the regulation and function of the Hippo pathway.
引用
收藏
页码:1 / 17
页数:17
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