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Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease
Prostate cancer (PCa) is a major diagnosed cancer among men globally, and about 20% of patients develop metastatic prostate cancer (mPCa) in the initial diagnosis. PCa is a typical androgen-dependent disease; thus, hormonal therapy is commonly used as a standard care for mPCa by inhibiting androgen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405166/ https://www.ncbi.nlm.nih.gov/pubmed/36009418 http://dx.doi.org/10.3390/biomedicines10081872 |
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author | Wang, Bo-Ren Chen, Yu-An Kao, Wei-Hsiang Lai, Chih-Ho Lin, Ho Hsieh, Jer-Tsong |
author_facet | Wang, Bo-Ren Chen, Yu-An Kao, Wei-Hsiang Lai, Chih-Ho Lin, Ho Hsieh, Jer-Tsong |
author_sort | Wang, Bo-Ren |
collection | PubMed |
description | Prostate cancer (PCa) is a major diagnosed cancer among men globally, and about 20% of patients develop metastatic prostate cancer (mPCa) in the initial diagnosis. PCa is a typical androgen-dependent disease; thus, hormonal therapy is commonly used as a standard care for mPCa by inhibiting androgen receptor (AR) activities, or androgen metabolism. Inevitably, almost all PCa will acquire resistance and become castration-resistant PCa (CRPC) that is associated with AR gene mutations or amplification, the presence of AR variants, loss of AR expression toward neuroendocrine phenotype, or other hormonal receptors. Treating CRPC poses a great challenge to clinicians. Research efforts in the last decade have come up with several new anti-androgen agents to prolong overall survival of CRPC patients. In addition, many potential targeting agents have been at the stage of being able to translate many preclinical discoveries into clinical practices. At this juncture, it is important to highlight the emerging strategies including small-molecule inhibitors to AR variants, DNA repair enzymes, cell survival pathway, neuroendocrine differentiation pathway, radiotherapy, CRPC-specific theranostics and immune therapy that are underway or have recently been completed. |
format | Online Article Text |
id | pubmed-9405166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94051662022-08-26 Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease Wang, Bo-Ren Chen, Yu-An Kao, Wei-Hsiang Lai, Chih-Ho Lin, Ho Hsieh, Jer-Tsong Biomedicines Review Prostate cancer (PCa) is a major diagnosed cancer among men globally, and about 20% of patients develop metastatic prostate cancer (mPCa) in the initial diagnosis. PCa is a typical androgen-dependent disease; thus, hormonal therapy is commonly used as a standard care for mPCa by inhibiting androgen receptor (AR) activities, or androgen metabolism. Inevitably, almost all PCa will acquire resistance and become castration-resistant PCa (CRPC) that is associated with AR gene mutations or amplification, the presence of AR variants, loss of AR expression toward neuroendocrine phenotype, or other hormonal receptors. Treating CRPC poses a great challenge to clinicians. Research efforts in the last decade have come up with several new anti-androgen agents to prolong overall survival of CRPC patients. In addition, many potential targeting agents have been at the stage of being able to translate many preclinical discoveries into clinical practices. At this juncture, it is important to highlight the emerging strategies including small-molecule inhibitors to AR variants, DNA repair enzymes, cell survival pathway, neuroendocrine differentiation pathway, radiotherapy, CRPC-specific theranostics and immune therapy that are underway or have recently been completed. MDPI 2022-08-03 /pmc/articles/PMC9405166/ /pubmed/36009418 http://dx.doi.org/10.3390/biomedicines10081872 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Wang, Bo-Ren Chen, Yu-An Kao, Wei-Hsiang Lai, Chih-Ho Lin, Ho Hsieh, Jer-Tsong Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title | Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title_full | Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title_fullStr | Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title_full_unstemmed | Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title_short | Developing New Treatment Options for Castration-Resistant Prostate Cancer and Recurrent Disease |
title_sort | developing new treatment options for castration-resistant prostate cancer and recurrent disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405166/ https://www.ncbi.nlm.nih.gov/pubmed/36009418 http://dx.doi.org/10.3390/biomedicines10081872 |
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