Your browser doesn't support javascript.
loading
The stress-regulated protein p8 mediates cannabinoid-induced apoptosis of tumor cells.
Carracedo, Arkaitz; Lorente, Mar; Egia, Ainara; Blázquez, Cristina; García, Stephane; Giroux, Valentin; Malicet, Cedric; Villuendas, Raquel; Gironella, Meritxell; González-Feria, Luis; Piris, Miguel Angel; Iovanna, Juan L; Guzmán, Manuel; Velasco, Guillermo.
Afiliação
  • Carracedo A; Department of Biochemistry and Molecular Biology I, School of Biology, Complutense University, 28040 Madrid, Spain.
Cancer Cell ; 9(4): 301-12, 2006 Apr.
Article em En | MEDLINE | ID: mdl-16616335
ABSTRACT
One of the most exciting areas of current research in the cannabinoid field is the study of the potential application of these compounds as antitumoral drugs. Here, we describe the signaling pathway that mediates cannabinoid-induced apoptosis of tumor cells. By using a wide array of experimental approaches, we identify the stress-regulated protein p8 (also designated as candidate of metastasis 1) as an essential mediator of cannabinoid antitumoral action and show that p8 upregulation is dependent on de novo-synthesized ceramide. We also observe that p8 mediates its apoptotic effect via upregulation of the endoplasmic reticulum stress-related genes ATF-4, CHOP, and TRB3. Activation of this pathway may constitute a potential therapeutic strategy for inhibiting tumor growth.
Assuntos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dronabinol / Canabinoides / Apoptose / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Proteínas de Neoplasias / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cancer Cell Ano de publicação: 2006 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dronabinol / Canabinoides / Apoptose / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Proteínas de Neoplasias / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Cancer Cell Ano de publicação: 2006 Tipo de documento: Article