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STRIPAK components determine mode of cancer cell migration and metastasis.
Madsen, Chris D; Hooper, Steven; Tozluoglu, Melda; Bruckbauer, Andreas; Fletcher, Georgina; Erler, Janine T; Bates, Paul A; Thompson, Barry; Sahai, Erik.
Afiliação
  • Madsen CD; 1] Tumour Cell Biology Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK [2] Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5 2200 Copenhagen N, Denmark.
  • Hooper S; Tumour Cell Biology Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK.
  • Tozluoglu M; Biomolecular Modelling Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK.
  • Bruckbauer A; Lymphocyte Interaction Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK.
  • Fletcher G; Epithelial Biology Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London, WC2A 3LY, UK.
  • Erler JT; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5 2200 Copenhagen N, Denmark.
  • Bates PA; Biomolecular Modelling Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK.
  • Thompson B; Epithelial Biology Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London, WC2A 3LY, UK.
  • Sahai E; Tumour Cell Biology Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields London WC2A 3LY, UK.
Nat Cell Biol ; 17(1): 68-80, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25531779
The contractile actomyosin cytoskeleton and its connection to the plasma membrane are critical for control of cell shape and migration. We identify three STRIPAK complex components, FAM40A, FAM40B and STRN3, as regulators of the actomyosin cortex. We show that FAM40A negatively regulates the MST3 and MST4 kinases, which promote the co-localization of the contractile actomyosin machinery with the Ezrin/Radixin/Moesin family proteins by phosphorylating the inhibitors of PPP1CB, PPP1R14A-D. Using computational modelling, in vitro cell migration assays and in vivo breast cancer metastasis assays we demonstrate that co-localization of contractile activity and actin-plasma membrane linkage reduces cell speed on planar surfaces, but favours migration in confined environments similar to those observed in vivo. We further show that FAM40B mutations found in human tumours uncouple it from PP2A and enable it to drive a contractile phenotype, which may underlie its role in human cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Autoantígenos / Proteínas de Ligação a Calmodulina / Neoplasias da Mama / Proteínas de Transporte Tipo de estudo: Prognostic_studies Idioma: En Revista: Nat Cell Biol Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Autoantígenos / Proteínas de Ligação a Calmodulina / Neoplasias da Mama / Proteínas de Transporte Tipo de estudo: Prognostic_studies Idioma: En Revista: Nat Cell Biol Ano de publicação: 2015 Tipo de documento: Article