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Willing to Be Involved in Cancer.
Gunn-Moore, Frank J; Tilston-Lünel, Andrew M; Reynolds, Paul A.
Afiliação
  • Gunn-Moore FJ; Medical and Biological Sciences Building, School of Biology, University of St Andrews, St Andrews KY16 9TF, UK. fjg1@st-andrews.ac.uk.
  • Tilston-Lünel AM; Medical and Biological Sciences Building, School of Biology, University of St Andrews, St Andrews KY16 9TF, UK. aml7@st-andrews.ac.uk.
  • Reynolds PA; Medical and Biological Sciences Building, School of Medicine, University of St Andrews, St Andrews KY16 9TF, UK. par10@st-andrews.ac.uk.
Genes (Basel) ; 7(7)2016 Jul 18.
Article em En | MEDLINE | ID: mdl-27438856
Genome sequencing is now a common procedure, but prior to this, screening experiments using protein baits was one of the routinely used methods that, occasionally, allowed the identification of new gene products. One such experiment uncovered the gene product called willin/human Expanded/FRMD6. Initial characterization studies found that willin bound phospholipids and was strongly co-localised with actin. However, subsequently, willin was found to be the closest human sequence homologue of the Drosophila protein Expanded (Ex), sharing 60% homology with the Ex FERM domain. This in turn suggested, and then was proven that willin could activate the Hippo signalling pathway. This review describes the increasing body of knowledge about the actions of willin in a number of cellular functions related to cancer. However, like many gene products involved in aspects of cell signalling, a convincing direct role for willin in cancer remains tantalisingly elusive, at present.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genes (Basel) Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Genes (Basel) Ano de publicação: 2016 Tipo de documento: Article