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Mechanisms of Hippo pathway regulation.
Meng, Zhipeng; Moroishi, Toshiro; Guan, Kun-Liang.
Afiliação
  • Meng Z; Department of Pharmacology, Moores Cancer Center, University of California at San Diego, La Jolla, California 92093, USA.
  • Moroishi T; Department of Pharmacology, Moores Cancer Center, University of California at San Diego, La Jolla, California 92093, USA.
  • Guan KL; Department of Pharmacology, Moores Cancer Center, University of California at San Diego, La Jolla, California 92093, USA.
Genes Dev ; 30(1): 1-17, 2016 Jan 01.
Article em En | MEDLINE | ID: mdl-26728553
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Regulação Enzimológica da Expressão Gênica / Proteínas Serina-Treonina Quinases Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Regulação Enzimológica da Expressão Gênica / Proteínas Serina-Treonina Quinases Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article