Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Bo-Ren, Chen, Yu-An, Kao, Wei-Hsiang, Lai, Chih-Ho, Lin, Ho, Hsieh, Jer-Tsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784773814114058240
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
work_keys_str_mv AT wangboren developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease
AT chenyuan developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease
AT kaoweihsiang developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease
AT laichihho developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease
AT linho developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease
AT hsiehjertsong developingnewtreatmentoptionsforcastrationresistantprostatecancerandrecurrentdisease