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Novel non-AR therapeutic targets in castrate resistant prostate cancer

Castrate resistant prostate cancer (CRPC) remains a disease with significant morbidity and mortality. The recent approval of abiraterone and enzalutamide highlight the improvements which can be made targeting the androgen receptor (AR) axis. Nonetheless, resistance inevitably develops and there is c...

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Detalles Bibliográficos
Autores principales: Toren, Paul J., Gleave, Martin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708177/
https://www.ncbi.nlm.nih.gov/pubmed/26816739
http://dx.doi.org/10.3978/j.issn.2223-4683.2013.09.09
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author Toren, Paul J.
Gleave, Martin E.
author_facet Toren, Paul J.
Gleave, Martin E.
author_sort Toren, Paul J.
collection PubMed
description Castrate resistant prostate cancer (CRPC) remains a disease with significant morbidity and mortality. The recent approval of abiraterone and enzalutamide highlight the improvements which can be made targeting the androgen receptor (AR) axis. Nonetheless, resistance inevitably develops and there is continued interest in targeting alternate pathways which cause disease resistance and progression. Here, we review non-AR targets in CRPC, with an emphasis on novel agents now in development. This includes therapeutics which target the tumour microenvironment, the bone metastatic environment, microtubules, cellular energetics, angiogenesis, the stress response, survival proteins, intracellular signal transduction, DNA damage repair and dendritic cells. Understanding the hallmarks of prostate cancer resistance in CRPC has led to the identification and development of these new targets. We review the molecular rationale, as well at the clinical experience for each of these different classes of agents which are in clinical development.
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spelling pubmed-47081772016-01-26 Novel non-AR therapeutic targets in castrate resistant prostate cancer Toren, Paul J. Gleave, Martin E. Transl Androl Urol Review Article Castrate resistant prostate cancer (CRPC) remains a disease with significant morbidity and mortality. The recent approval of abiraterone and enzalutamide highlight the improvements which can be made targeting the androgen receptor (AR) axis. Nonetheless, resistance inevitably develops and there is continued interest in targeting alternate pathways which cause disease resistance and progression. Here, we review non-AR targets in CRPC, with an emphasis on novel agents now in development. This includes therapeutics which target the tumour microenvironment, the bone metastatic environment, microtubules, cellular energetics, angiogenesis, the stress response, survival proteins, intracellular signal transduction, DNA damage repair and dendritic cells. Understanding the hallmarks of prostate cancer resistance in CRPC has led to the identification and development of these new targets. We review the molecular rationale, as well at the clinical experience for each of these different classes of agents which are in clinical development. AME Publishing Company 2013-09 /pmc/articles/PMC4708177/ /pubmed/26816739 http://dx.doi.org/10.3978/j.issn.2223-4683.2013.09.09 Text en 2013 Translational Andrology and Urology. All rights reserved.
spellingShingle Review Article
Toren, Paul J.
Gleave, Martin E.
Novel non-AR therapeutic targets in castrate resistant prostate cancer
title Novel non-AR therapeutic targets in castrate resistant prostate cancer
title_full Novel non-AR therapeutic targets in castrate resistant prostate cancer
title_fullStr Novel non-AR therapeutic targets in castrate resistant prostate cancer
title_full_unstemmed Novel non-AR therapeutic targets in castrate resistant prostate cancer
title_short Novel non-AR therapeutic targets in castrate resistant prostate cancer
title_sort novel non-ar therapeutic targets in castrate resistant prostate cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708177/
https://www.ncbi.nlm.nih.gov/pubmed/26816739
http://dx.doi.org/10.3978/j.issn.2223-4683.2013.09.09
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