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PELP1: a review of PELP1 interactions, signaling, and biology.
Girard, Brian J; Daniel, Andrea R; Lange, Carol A; Ostrander, Julie H.
Afiliação
  • Girard BJ; Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
  • Daniel AR; Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
  • Lange CA; Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.
  • Ostrander JH; Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States. Electronic address: hans1354@umn.edu.
Mol Cell Endocrinol ; 382(1): 642-651, 2014 Jan 25.
Article em En | MEDLINE | ID: mdl-23933151
Proline, glutamic acid, and leucine rich protein 1 (PELP1) is a large multi-domain protein that has been shown to modulate an increasing number of pathways and biological processes. The first reports describing the cloning and characterization of PELP1 showed that it was an estrogen receptor coactivator. PELP1 has now been shown to be a coregulator for a growing number of transcription factors. Furthermore, recent reports have shown that PELP1 is a member of chromatin remodeling complexes. In addition to PELP1 nuclear functions, it has been shown to have cytoplasmic signaling functions as well. In the cytoplasm PELP1 acts as a scaffold molecule and mediates rapid signaling from growth factor and hormone receptors. PELP1 signaling ultimately plays a role in cancer biology by increasing proliferation and metastasis, among other cellular processes. Here we will review (1) the cloning and characterization of PELP1 expression, (2) interacting proteins, (3) PELP1 signaling, and (4) PELP1-mediated biology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transdução de Sinais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transdução de Sinais Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos