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Role of taxanes in advanced prostate cancer
Cassinello, J; Carballido Rodríguez, J; Antón Aparicio, L.
Afiliación
  • Cassinello, J; Guadalajara University Hospital. Medical Oncology Service. Guadalajara. Spain
  • Carballido Rodríguez, J; Puerta de Hierro University Hospital. Urology Service. Madrid. Spain
  • Antón Aparicio, L; Complexo Hospitalario Universitario A Coruña . Medical Oncology Service. A Coruña. Spain
Clin. transl. oncol. (Print) ; 18(10): 972-980, oct. 2016. ilus
Article en En | IBECS | ID: ibc-155959
Biblioteca responsable: ES1.1
Ubicación: BNCS
ABSTRACT
Advanced prostate cancer is an androgen-dependent disease for which the initial treatment is an androgen deprivation maneuver. However, some primary resistances to hormonal treatment occur with increasing incidence throughout the evolution of the disease. The taxanes, docetaxel and cabazitaxel, exert their action at multiple levels at the tumor cell besides inhibiting the mitosis and inducing the cell death, they induce the nuclear accumulation of FOXO1, a potent nuclear factor that acts against the activation of androgen receptor inhibiting the transcription of AR-V7 variant associated with the development of resistances to abiraterone and enzalutamide. Docetaxel, as first-line therapy, and cabazitaxel, as secondline therapy, have demonstrated to increase the survival in castration-resistant prostate cancer. The results from last studies either on high-risk localized disease or on androgen-sensitive tumors demonstrate the increasing role of taxanes at earlier states of prostate cancer (AU)
RESUMEN
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Asunto(s)
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Colección: 06-national / ES Base de datos: IBECS Asunto principal: Neoplasias de la Próstata / Taxoides / Antagonistas de Andrógenos Tipo de estudio: Etiology_studies Límite: Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2016 Tipo del documento: Article
Buscar en Google
Colección: 06-national / ES Base de datos: IBECS Asunto principal: Neoplasias de la Próstata / Taxoides / Antagonistas de Andrógenos Tipo de estudio: Etiology_studies Límite: Humans / Male Idioma: En Revista: Clin. transl. oncol. (Print) Año: 2016 Tipo del documento: Article
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