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Molecular mechanisms of enzalutamide resistance in prostate cancer

An estimated 30,000 men in the United States will die of metastatic prostate cancer (PCa) each year due to the development of therapy resistance, most notably resistance to second-generation antiandrogen enzalutamide. The vast majority of PCa is driven by the androgen receptor (AR). Enzalutamide is...

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Detalles Bibliográficos
Autores principales: Blatt, Eliot B., Raj, Ganesh V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OAE Publishing Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992629/
https://www.ncbi.nlm.nih.gov/pubmed/35582713
http://dx.doi.org/10.20517/cdr.2019.25
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author Blatt, Eliot B.
Raj, Ganesh V.
author_facet Blatt, Eliot B.
Raj, Ganesh V.
author_sort Blatt, Eliot B.
collection PubMed
description An estimated 30,000 men in the United States will die of metastatic prostate cancer (PCa) each year due to the development of therapy resistance, most notably resistance to second-generation antiandrogen enzalutamide. The vast majority of PCa is driven by the androgen receptor (AR). Enzalutamide is an AR antagonist, which extends patient survival and is widely used in the clinic for the treatment of castration-resistant prostate cancer (CRPC); however, many patients will have primary or develop acquired resistance and continue to progress. Characterization of the molecular mechanisms of enzalutamide resistance provides insight into potentially efficacious therapies for enzalutamide-resistant CRPC (ER-CRPC). Understanding these mechanisms is critical for the identification of biomarkers predictive of therapy resistance and the development of therapeutic strategies to target ER-CRPC.
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spelling pubmed-89926292022-05-16 Molecular mechanisms of enzalutamide resistance in prostate cancer Blatt, Eliot B. Raj, Ganesh V. Cancer Drug Resist Review An estimated 30,000 men in the United States will die of metastatic prostate cancer (PCa) each year due to the development of therapy resistance, most notably resistance to second-generation antiandrogen enzalutamide. The vast majority of PCa is driven by the androgen receptor (AR). Enzalutamide is an AR antagonist, which extends patient survival and is widely used in the clinic for the treatment of castration-resistant prostate cancer (CRPC); however, many patients will have primary or develop acquired resistance and continue to progress. Characterization of the molecular mechanisms of enzalutamide resistance provides insight into potentially efficacious therapies for enzalutamide-resistant CRPC (ER-CRPC). Understanding these mechanisms is critical for the identification of biomarkers predictive of therapy resistance and the development of therapeutic strategies to target ER-CRPC. OAE Publishing Inc. 2019-06-19 /pmc/articles/PMC8992629/ /pubmed/35582713 http://dx.doi.org/10.20517/cdr.2019.25 Text en © The Author(s) 2019. https://creativecommons.org/licenses/by/4.0/© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Blatt, Eliot B.
Raj, Ganesh V.
Molecular mechanisms of enzalutamide resistance in prostate cancer
title Molecular mechanisms of enzalutamide resistance in prostate cancer
title_full Molecular mechanisms of enzalutamide resistance in prostate cancer
title_fullStr Molecular mechanisms of enzalutamide resistance in prostate cancer
title_full_unstemmed Molecular mechanisms of enzalutamide resistance in prostate cancer
title_short Molecular mechanisms of enzalutamide resistance in prostate cancer
title_sort molecular mechanisms of enzalutamide resistance in prostate cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992629/
https://www.ncbi.nlm.nih.gov/pubmed/35582713
http://dx.doi.org/10.20517/cdr.2019.25
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