Your browser doesn't support javascript.
loading
A cancer-associated, genome protective programme engaging PKCε.
Parker, Peter J; Lockwood, Nicola; Davis, Khalil; Kelly, Joanna R; Soliman, Tanya N; Pardo, Ainara Lopez; Marshall, Jacqueline J T; Redmond, Joanna M; Vitale, Marco.
Afiliação
  • Parker PJ; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK; School of Cancer and Pharmaceutical Sciences, Guy's Campus, London, SE1 1UL, UK. Electronic address: peter.parker@crick.ac.uk.
  • Lockwood N; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK.
  • Davis K; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK.
  • Kelly JR; Cancer Research UK, Manchester Institute, Alderley Park, SK10 4TG, UK.
  • Soliman TN; Barts Cancer Institute, Charterhouse Square, London, EC1M 6BE, UK.
  • Pardo AL; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK.
  • Marshall JJT; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK.
  • Redmond JM; GSK, Stevenage, Hertfordshire, SG1 2NY, UK.
  • Vitale M; Department of Medicine and Surgery, University of Parma, Parma, Italy.
  • Silvia Martini; Protein Phosphorylation Laboratory, Francis Crick Institute, London, NW1 1AT, UK.
Adv Biol Regul ; 78: 100759, 2020 12.
Article em En | MEDLINE | ID: mdl-33039823
ABSTRACT
Associated with their roles as targets for tumour promoters, there has been a long-standing interest in how members of the protein kinase C (PKC) family act to modulate cell growth and division. This has generated a great deal of observational data, but has for the most part not afforded clear mechanistic insights into the control mechanisms at play. Here, we review the roles of PKCε in protecting transformed cells from non-disjunction. In this particular cell cycle context, there is a growing understanding of the pathways involved, affording biomarker and interventional insights and opportunities.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genômica / Proteína Quinase C-épsilon / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Adv Biol Regul Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genômica / Proteína Quinase C-épsilon / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Adv Biol Regul Ano de publicação: 2020 Tipo de documento: Article