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Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment

Patients with castration-resistant prostate cancer (CRPC), who progress after docetaxel therapy, had until very recently, only a few therapeutic options. Recent advances in this field brought about new perspectives in the treatment of this disease. Molecular, basic, and translational research has gi...

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Detalles Bibliográficos
Autores principales: Amaral, Teresa Maria Santos, Macedo, Daniela, Fernandes, Isabel, Costa, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316959/
https://www.ncbi.nlm.nih.gov/pubmed/22530130
http://dx.doi.org/10.1155/2012/327253
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author Amaral, Teresa Maria Santos
Macedo, Daniela
Fernandes, Isabel
Costa, Luis
author_facet Amaral, Teresa Maria Santos
Macedo, Daniela
Fernandes, Isabel
Costa, Luis
author_sort Amaral, Teresa Maria Santos
collection PubMed
description Patients with castration-resistant prostate cancer (CRPC), who progress after docetaxel therapy, had until very recently, only a few therapeutic options. Recent advances in this field brought about new perspectives in the treatment of this disease. Molecular, basic, and translational research has given us a better understanding on the mechanisms of CRPC. This great investment has turned into a more rational approach to the development of new drugs. Some of the new treatments are already available to our patients outside clinical trials and may include inhibitors of androgen biosynthesis; new chemotherapy agents; bone-targeted therapy; and immunotherapy. This paper aims to review the mechanisms of prostate cancer resistance, possible therapeutic targets, as well as new options to treat CRPC.
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spelling pubmed-33169592012-04-23 Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment Amaral, Teresa Maria Santos Macedo, Daniela Fernandes, Isabel Costa, Luis Prostate Cancer Review Article Patients with castration-resistant prostate cancer (CRPC), who progress after docetaxel therapy, had until very recently, only a few therapeutic options. Recent advances in this field brought about new perspectives in the treatment of this disease. Molecular, basic, and translational research has given us a better understanding on the mechanisms of CRPC. This great investment has turned into a more rational approach to the development of new drugs. Some of the new treatments are already available to our patients outside clinical trials and may include inhibitors of androgen biosynthesis; new chemotherapy agents; bone-targeted therapy; and immunotherapy. This paper aims to review the mechanisms of prostate cancer resistance, possible therapeutic targets, as well as new options to treat CRPC. Hindawi Publishing Corporation 2012 2012-03-05 /pmc/articles/PMC3316959/ /pubmed/22530130 http://dx.doi.org/10.1155/2012/327253 Text en Copyright © 2012 Teresa Maria Santos Amaral et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Amaral, Teresa Maria Santos
Macedo, Daniela
Fernandes, Isabel
Costa, Luis
Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title_full Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title_fullStr Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title_full_unstemmed Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title_short Castration-Resistant Prostate Cancer: Mechanisms, Targets, and Treatment
title_sort castration-resistant prostate cancer: mechanisms, targets, and treatment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316959/
https://www.ncbi.nlm.nih.gov/pubmed/22530130
http://dx.doi.org/10.1155/2012/327253
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