Loading…
Promising therapy for neuroendocrine prostate cancer: current status and future directions
Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatmen...
Saved in:
Published in: | Therapeutic advances in medical oncology 2024-01, Vol.16, p.17588359241269676 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c316t-fe23081daa87d06c23be766753085743639108daec250332c8f58f132effb0cc3 |
container_end_page | |
container_issue | |
container_start_page | 17588359241269676 |
container_title | Therapeutic advances in medical oncology |
container_volume | 16 |
creator | Fei, Xin Xue, Jia-Wei Wu, Ji-zhongrong Yang, Chong-Yi Wang, Ke-Jie Ma, Qi |
description | Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatment of androgen deprivation therapy and androgen receptor pathway inhibitors (ARPIs). Currently, the treatment of NEPC follows the treatment strategy for small-cell lung cancer, lacking effective drugs and specific treatment options. This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (zeste homolog 2 inhibitors, lysine-specific demethylase 1 inhibitors), aurora kinase A inhibitors, poly-ADP-ribose polymerase inhibitors, delta-like ligand 3 targeted therapies, a combination of immunotherapies, etc. Other promising targets and future directions are also discussed in this review. These novel targets and therapies may provide new opportunities for the treatment of NEPC.
Plain language summary
This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (EZH2 inhibitors, LSD-1 inhibitors), AURKA inhibitors, PARP inhibitors, and DLL3 targeted therapies, and combination of immunotherapies, etc. These novel targets and therapies may provide new opportunities in the treatment of NEPC. |
doi_str_mv | 10.1177/17588359241269676 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_59b05bcbddda4fbf87325fdeb6200a2f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_17588359241269676</sage_id><doaj_id>oai_doaj_org_article_59b05bcbddda4fbf87325fdeb6200a2f</doaj_id><sourcerecordid>3092013799</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-fe23081daa87d06c23be766753085743639108daec250332c8f58f132effb0cc3</originalsourceid><addsrcrecordid>eNp1kTtvVDEQha0IRB7wA9IgSzRpNvhxbV_ToSgvKRIU0NBYvvZ4uatde_GjyL-Plw1JBKLy6Oib45k5CJ1Sck6pUh-pEuPIhWYDZVJLJQ_Q0U5b7MRXL-pDdFzKihApB0neoEOuKaeKqSP042tOm7nMcYnrT8h2e49DyjhCywmiTy7PEfA2p1JtBexsdJA_YddyhljxTm0F2-hxaLVlwH7O4OqcYnmLXge7LvDu8T1B368uv13cLO6-XN9efL5bOE5lXQRgnIzUWzsqT6RjfAIlpRJdFWrgsg9LRm_BMUE4Z24MYgyUMwhhIs7xE3S79_XJrsw2zxub702ys_ktpLw0NtfZrcEIPRExucl7b4cwhVFxJoKHSTJCLAvd62zv1Tf-1aBU04_jYL22EVIrhhPNCOVK645--AtdpZZj39RwOmgltSKyU3RPuX7CkiE8DUiJ2YVo_gmx97x_dG7TBvxTx5_UOnC-B4pdwvO3_3d8AA5apNo</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3149769706</pqid></control><display><type>article</type><title>Promising therapy for neuroendocrine prostate cancer: current status and future directions</title><source>Open Access: PubMed Central</source><source>SAGE Open Access Journals</source><source>Publicly Available Content (ProQuest)</source><creator>Fei, Xin ; Xue, Jia-Wei ; Wu, Ji-zhongrong ; Yang, Chong-Yi ; Wang, Ke-Jie ; Ma, Qi</creator><creatorcontrib>Fei, Xin ; Xue, Jia-Wei ; Wu, Ji-zhongrong ; Yang, Chong-Yi ; Wang, Ke-Jie ; Ma, Qi</creatorcontrib><description>Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatment of androgen deprivation therapy and androgen receptor pathway inhibitors (ARPIs). Currently, the treatment of NEPC follows the treatment strategy for small-cell lung cancer, lacking effective drugs and specific treatment options. This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (zeste homolog 2 inhibitors, lysine-specific demethylase 1 inhibitors), aurora kinase A inhibitors, poly-ADP-ribose polymerase inhibitors, delta-like ligand 3 targeted therapies, a combination of immunotherapies, etc. Other promising targets and future directions are also discussed in this review. These novel targets and therapies may provide new opportunities for the treatment of NEPC.
Plain language summary
This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (EZH2 inhibitors, LSD-1 inhibitors), AURKA inhibitors, PARP inhibitors, and DLL3 targeted therapies, and combination of immunotherapies, etc. These novel targets and therapies may provide new opportunities in the treatment of NEPC.</description><identifier>ISSN: 1758-8359</identifier><identifier>ISSN: 1758-8340</identifier><identifier>EISSN: 1758-8359</identifier><identifier>DOI: 10.1177/17588359241269676</identifier><identifier>PMID: 39131727</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Androgen receptors ; Aurora kinase ; Castration ; Epigenetics ; Immunotherapy ; Phenotypes ; Prostate cancer ; Small cell lung carcinoma</subject><ispartof>Therapeutic advances in medical oncology, 2024-01, Vol.16, p.17588359241269676</ispartof><rights>The Author(s), 2024</rights><rights>The Author(s), 2024.</rights><rights>The Author(s), 2024. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c316t-fe23081daa87d06c23be766753085743639108daec250332c8f58f132effb0cc3</cites><orcidid>0000-0002-5350-0362</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/17588359241269676$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3149769706?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>313,314,780,784,792,21957,25744,27844,27913,27915,27916,37003,37004,44581,44936,45324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39131727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fei, Xin</creatorcontrib><creatorcontrib>Xue, Jia-Wei</creatorcontrib><creatorcontrib>Wu, Ji-zhongrong</creatorcontrib><creatorcontrib>Yang, Chong-Yi</creatorcontrib><creatorcontrib>Wang, Ke-Jie</creatorcontrib><creatorcontrib>Ma, Qi</creatorcontrib><title>Promising therapy for neuroendocrine prostate cancer: current status and future directions</title><title>Therapeutic advances in medical oncology</title><addtitle>Ther Adv Med Oncol</addtitle><description>Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatment of androgen deprivation therapy and androgen receptor pathway inhibitors (ARPIs). Currently, the treatment of NEPC follows the treatment strategy for small-cell lung cancer, lacking effective drugs and specific treatment options. This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (zeste homolog 2 inhibitors, lysine-specific demethylase 1 inhibitors), aurora kinase A inhibitors, poly-ADP-ribose polymerase inhibitors, delta-like ligand 3 targeted therapies, a combination of immunotherapies, etc. Other promising targets and future directions are also discussed in this review. These novel targets and therapies may provide new opportunities for the treatment of NEPC.
Plain language summary
This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (EZH2 inhibitors, LSD-1 inhibitors), AURKA inhibitors, PARP inhibitors, and DLL3 targeted therapies, and combination of immunotherapies, etc. These novel targets and therapies may provide new opportunities in the treatment of NEPC.</description><subject>Androgen receptors</subject><subject>Aurora kinase</subject><subject>Castration</subject><subject>Epigenetics</subject><subject>Immunotherapy</subject><subject>Phenotypes</subject><subject>Prostate cancer</subject><subject>Small cell lung carcinoma</subject><issn>1758-8359</issn><issn>1758-8340</issn><issn>1758-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kTtvVDEQha0IRB7wA9IgSzRpNvhxbV_ToSgvKRIU0NBYvvZ4uatde_GjyL-Plw1JBKLy6Oib45k5CJ1Sck6pUh-pEuPIhWYDZVJLJQ_Q0U5b7MRXL-pDdFzKihApB0neoEOuKaeKqSP042tOm7nMcYnrT8h2e49DyjhCywmiTy7PEfA2p1JtBexsdJA_YddyhljxTm0F2-hxaLVlwH7O4OqcYnmLXge7LvDu8T1B368uv13cLO6-XN9efL5bOE5lXQRgnIzUWzsqT6RjfAIlpRJdFWrgsg9LRm_BMUE4Z24MYgyUMwhhIs7xE3S79_XJrsw2zxub702ys_ktpLw0NtfZrcEIPRExucl7b4cwhVFxJoKHSTJCLAvd62zv1Tf-1aBU04_jYL22EVIrhhPNCOVK645--AtdpZZj39RwOmgltSKyU3RPuX7CkiE8DUiJ2YVo_gmx97x_dG7TBvxTx5_UOnC-B4pdwvO3_3d8AA5apNo</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Fei, Xin</creator><creator>Xue, Jia-Wei</creator><creator>Wu, Ji-zhongrong</creator><creator>Yang, Chong-Yi</creator><creator>Wang, Ke-Jie</creator><creator>Ma, Qi</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5350-0362</orcidid></search><sort><creationdate>20240101</creationdate><title>Promising therapy for neuroendocrine prostate cancer: current status and future directions</title><author>Fei, Xin ; Xue, Jia-Wei ; Wu, Ji-zhongrong ; Yang, Chong-Yi ; Wang, Ke-Jie ; Ma, Qi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-fe23081daa87d06c23be766753085743639108daec250332c8f58f132effb0cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Androgen receptors</topic><topic>Aurora kinase</topic><topic>Castration</topic><topic>Epigenetics</topic><topic>Immunotherapy</topic><topic>Phenotypes</topic><topic>Prostate cancer</topic><topic>Small cell lung carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fei, Xin</creatorcontrib><creatorcontrib>Xue, Jia-Wei</creatorcontrib><creatorcontrib>Wu, Ji-zhongrong</creatorcontrib><creatorcontrib>Yang, Chong-Yi</creatorcontrib><creatorcontrib>Wang, Ke-Jie</creatorcontrib><creatorcontrib>Ma, Qi</creatorcontrib><collection>SAGE Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Directory of Open Access Journals</collection><jtitle>Therapeutic advances in medical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fei, Xin</au><au>Xue, Jia-Wei</au><au>Wu, Ji-zhongrong</au><au>Yang, Chong-Yi</au><au>Wang, Ke-Jie</au><au>Ma, Qi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Promising therapy for neuroendocrine prostate cancer: current status and future directions</atitle><jtitle>Therapeutic advances in medical oncology</jtitle><addtitle>Ther Adv Med Oncol</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>16</volume><spage>17588359241269676</spage><pages>17588359241269676-</pages><issn>1758-8359</issn><issn>1758-8340</issn><eissn>1758-8359</eissn><abstract>Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatment of androgen deprivation therapy and androgen receptor pathway inhibitors (ARPIs). Currently, the treatment of NEPC follows the treatment strategy for small-cell lung cancer, lacking effective drugs and specific treatment options. This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (zeste homolog 2 inhibitors, lysine-specific demethylase 1 inhibitors), aurora kinase A inhibitors, poly-ADP-ribose polymerase inhibitors, delta-like ligand 3 targeted therapies, a combination of immunotherapies, etc. Other promising targets and future directions are also discussed in this review. These novel targets and therapies may provide new opportunities for the treatment of NEPC.
Plain language summary
This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (EZH2 inhibitors, LSD-1 inhibitors), AURKA inhibitors, PARP inhibitors, and DLL3 targeted therapies, and combination of immunotherapies, etc. These novel targets and therapies may provide new opportunities in the treatment of NEPC.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>39131727</pmid><doi>10.1177/17588359241269676</doi><orcidid>https://orcid.org/0000-0002-5350-0362</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1758-8359 |
ispartof | Therapeutic advances in medical oncology, 2024-01, Vol.16, p.17588359241269676 |
issn | 1758-8359 1758-8340 1758-8359 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_59b05bcbddda4fbf87325fdeb6200a2f |
source | Open Access: PubMed Central; SAGE Open Access Journals; Publicly Available Content (ProQuest) |
subjects | Androgen receptors Aurora kinase Castration Epigenetics Immunotherapy Phenotypes Prostate cancer Small cell lung carcinoma |
title | Promising therapy for neuroendocrine prostate cancer: current status and future directions |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A32%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Promising%20therapy%20for%20neuroendocrine%20prostate%20cancer:%20current%20status%20and%20future%20directions&rft.jtitle=Therapeutic%20advances%20in%20medical%20oncology&rft.au=Fei,%20Xin&rft.date=2024-01-01&rft.volume=16&rft.spage=17588359241269676&rft.pages=17588359241269676-&rft.issn=1758-8359&rft.eissn=1758-8359&rft_id=info:doi/10.1177/17588359241269676&rft_dat=%3Cproquest_doaj_%3E3092013799%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c316t-fe23081daa87d06c23be766753085743639108daec250332c8f58f132effb0cc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3149769706&rft_id=info:pmid/39131727&rft_sage_id=10.1177_17588359241269676&rfr_iscdi=true |