Literature DB >> 21874053

Integrating developmental signals: a Hippo in the (path)way.

A Mauviel1, F Nallet-Staub, X Varelas.   

Abstract

The Hippo pathway, a signaling cascade that controls cell cycle progression, apoptosis and cell differentiation, has emerged as a fundamental regulator of many physiological and pathological processes. Recent studies have revealed a complex network of interactions directing Hippo pathway activity, and have connected this pathway with other key signaling pathways. Such crosstalk has uncovered novel roles for Hippo signaling, including regulation of TGFβ/SMAD and WNT/β-catenin pathways. This review highlights some of the recent findings in the Hippo field with an emphasis on how the Hippo pathway is integrated with other pathways to mediate diverse processes.

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Year:  2011        PMID: 21874053     DOI: 10.1038/onc.2011.363

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  54 in total

1.  Xtalk: a path-based approach for identifying crosstalk between signaling pathways.

Authors:  Allison N Tegge; Nicholas Sharp; T M Murali
Journal:  Bioinformatics       Date:  2015-09-23       Impact factor: 6.937

2.  YAP and TAZ are distinct effectors of corneal myofibroblast transformation.

Authors:  Santoshi Muppala; Vijay Krishna Raghunathan; Iman Jalilian; Sara Thomasy; Christopher J Murphy
Journal:  Exp Eye Res       Date:  2018-12-19       Impact factor: 3.467

3.  TGF-β1 regulates the expression and transcriptional activity of TAZ protein via a Smad3-independent, myocardin-related transcription factor-mediated mechanism.

Authors:  Maria Zena Miranda; Janne Folke Bialik; Pam Speight; Qinghong Dan; Tony Yeung; Katalin Szászi; Stine F Pedersen; András Kapus
Journal:  J Biol Chem       Date:  2017-07-24       Impact factor: 5.157

4.  Mechanosignaling through YAP and TAZ drives fibroblast activation and fibrosis.

Authors:  Fei Liu; David Lagares; Kyoung Moo Choi; Lauren Stopfer; Aleksandar Marinković; Vladimir Vrbanac; Clemens K Probst; Samantha E Hiemer; Thomas H Sisson; Jeffrey C Horowitz; Ivan O Rosas; Laura E Fredenburgh; Carol Feghali-Bostwick; Xaralabos Varelas; Andrew M Tager; Daniel J Tschumperlin
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-12-12       Impact factor: 5.464

5.  Yap and its subcellular localization have distinct compartment-specific roles in the developing lung.

Authors:  Benjamin J van Soldt; Jun Qian; Jiao Li; Nan Tang; Jining Lu; Wellington V Cardoso
Journal:  Development       Date:  2019-05-01       Impact factor: 6.868

6.  Impaired Hippo signaling promotes Rho1-JNK-dependent growth.

Authors:  Xianjue Ma; Yujun Chen; Wenyan Xu; Nana Wu; Maoquan Li; Ying Cao; Shian Wu; Qiutang Li; Lei Xue
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-12       Impact factor: 11.205

7.  Epithelial-mesenchymal transition in colorectal cancer tissue of patients with Lynch syndrome.

Authors:  Guo-Li Gu; Xiao-Quan Zhu; Xue-Ming Wei; Li Ren; De-Chang Li; Shi-Lin Wang
Journal:  World J Gastroenterol       Date:  2014-01-07       Impact factor: 5.742

8.  Cell density sensing alters TGF-β signaling in a cell-type-specific manner, independent from Hippo pathway activation.

Authors:  Flore Nallet-Staub; Xueqian Yin; Cristèle Gilbert; Véronique Marsaud; Saber Ben Mimoun; Delphine Javelaud; Edward B Leof; Alain Mauviel
Journal:  Dev Cell       Date:  2015-03-09       Impact factor: 12.270

9.  LKB1 tumor suppressor regulates AMP kinase/mTOR-independent cell growth and proliferation via the phosphorylation of Yap.

Authors:  H B Nguyen; J T Babcock; C D Wells; L A Quilliam
Journal:  Oncogene       Date:  2012-10-01       Impact factor: 9.867

10.  The differential effects of wild-type and mutated K-Ras on MST2 signaling are determined by K-Ras activation kinetics.

Authors:  David Romano; Helene Maccario; Carolanne Doherty; Niall P Quinn; Walter Kolch; David Matallanas
Journal:  Mol Cell Biol       Date:  2013-03-04       Impact factor: 4.272

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