Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/48422
Título: | Transition to androgen-independence in prostate cancer | Autores/as: | Navarro Bosch, Domingo Luzardo, Octavio P. Fernández, Leandro Chesa, Nicolás Díaz-Chico, Bonifacio N. |
Clasificación UNESCO: | 32 Ciencias médicas 320101 Oncología |
Palabras clave: | Receptor Gene Amplification In-Situ Hybridization Rat Liver-Microsomes Therapy Failure Antiandrogen Withdrawal, et al. |
Fecha de publicación: | 2002 | Publicación seriada: | Journal of Steroid Biochemistry and Molecular Biology | Resumen: | Prostate carcinoma is the most frequently diagnosed malignancy and the second leading cause of death as a result of cancer in men in the western countries. Withdrawal of androgens or the peripheral blockage of androgen action remain the critical therapeutic options for the treatment of advanced prostate cancer. However. after initial regression, most of the prostate cancers become androgen-independent and progress further with eventual fatal outcome. Understanding the mechanisms of transition to androgen independence and tumor progression in prostate cancer is critical to finding new ways to treat aged patients that are ineligible for conventional chemotherapy. A large number of different molecular mechanisms might be responsible for the transition to androgen-independence. Many of these involve the androgen receptor (AR) and its signalling pathways. but they might also include genetic chances that affect several genes, which results in the activation of oncogenes or the inactivation of tumor suppressor genes. Here. we discuss the Most recent and relevant findings on androgen resistance in prostate cancer in order provide a comprehensive interpretation of the clinical behaviour of tumors at molecular levels. | URI: | http://hdl.handle.net/10553/48422 | ISSN: | 0960-0760 | DOI: | 10.1016/S0960-0760(02)00064-X | Fuente: | Journal of Steroid Biochemistry and Molecular Biology[ISSN 0960-0760],v. 81, p. 191-201 |
Colección: | Comentario |
Citas SCOPUSTM
85
actualizado el 15-dic-2024
Citas de WEB OF SCIENCETM
Citations
79
actualizado el 15-dic-2024
Visitas
78
actualizado el 13-jul-2024
Google ScholarTM
Verifica
Altmetric
Comparte
Exporta metadatos
Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.