Cargando…

Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin

Prostate cancer (PCa) patients who progress to metastatic castration-resistant PCa (mCRPC) mostly have poor outcomes due to the lack of effective therapies. Our recent study established the orphan nuclear receptor RORγ as a novel therapeutic target for CRPC. Here, we reveal that elaiophylin (Elai),...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Jianwei, Wang, Junfeng, Wang, Qian, Zou, Hongye, Wang, Hong, Zhang, Zhenhua, Chen, Jianghe, Wang, Qianqian, Wang, Panxia, Zhao, Yueshan, Lu, Jing, Zhang, Xiaolei, Xiang, Songtao, Wang, Haibin, Lei, Jinping, Chen, Hong-Wu, Liu, Peiqing, Liu, Yonghong, Han, Fanghai, Wang, Junjian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745055/
https://www.ncbi.nlm.nih.gov/pubmed/33354503
http://dx.doi.org/10.1016/j.apsb.2020.07.001
_version_ 1783624539562835968
author Zheng, Jianwei
Wang, Junfeng
Wang, Qian
Zou, Hongye
Wang, Hong
Zhang, Zhenhua
Chen, Jianghe
Wang, Qianqian
Wang, Panxia
Zhao, Yueshan
Lu, Jing
Zhang, Xiaolei
Xiang, Songtao
Wang, Haibin
Lei, Jinping
Chen, Hong-Wu
Liu, Peiqing
Liu, Yonghong
Han, Fanghai
Wang, Junjian
author_facet Zheng, Jianwei
Wang, Junfeng
Wang, Qian
Zou, Hongye
Wang, Hong
Zhang, Zhenhua
Chen, Jianghe
Wang, Qianqian
Wang, Panxia
Zhao, Yueshan
Lu, Jing
Zhang, Xiaolei
Xiang, Songtao
Wang, Haibin
Lei, Jinping
Chen, Hong-Wu
Liu, Peiqing
Liu, Yonghong
Han, Fanghai
Wang, Junjian
author_sort Zheng, Jianwei
collection PubMed
description Prostate cancer (PCa) patients who progress to metastatic castration-resistant PCa (mCRPC) mostly have poor outcomes due to the lack of effective therapies. Our recent study established the orphan nuclear receptor RORγ as a novel therapeutic target for CRPC. Here, we reveal that elaiophylin (Elai), an antibiotic from Actinomycete streptomyces, is a novel RORγ antagonist and showed potent antitumor activity against CRPC in vitro and in vivo. We demonstrated that Elai selectively binded to RORγ protein and potently blocked RORγ transcriptional regulation activities. Structure–activity relationship studies showed that Elai occupied the binding pocket with several key interactions. Furthermore, Elai markedly reduced the recruitment of RORγ to its genomic DNA response element (RORE), suppressed the expression of RORγ target genes AR and AR variants, and significantly inhibited PCa cell growth. Importantly, Elai strongly suppressed tumor growth in both cell line based and patient-derived PCa xenograft models. Taken together, these results suggest that Elai is novel therapeutic RORγ inhibitor that can be used as a drug candidate for the treatment of human CRPC.
format Online
Article
Text
id pubmed-7745055
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-77450552020-12-21 Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin Zheng, Jianwei Wang, Junfeng Wang, Qian Zou, Hongye Wang, Hong Zhang, Zhenhua Chen, Jianghe Wang, Qianqian Wang, Panxia Zhao, Yueshan Lu, Jing Zhang, Xiaolei Xiang, Songtao Wang, Haibin Lei, Jinping Chen, Hong-Wu Liu, Peiqing Liu, Yonghong Han, Fanghai Wang, Junjian Acta Pharm Sin B Original Article Prostate cancer (PCa) patients who progress to metastatic castration-resistant PCa (mCRPC) mostly have poor outcomes due to the lack of effective therapies. Our recent study established the orphan nuclear receptor RORγ as a novel therapeutic target for CRPC. Here, we reveal that elaiophylin (Elai), an antibiotic from Actinomycete streptomyces, is a novel RORγ antagonist and showed potent antitumor activity against CRPC in vitro and in vivo. We demonstrated that Elai selectively binded to RORγ protein and potently blocked RORγ transcriptional regulation activities. Structure–activity relationship studies showed that Elai occupied the binding pocket with several key interactions. Furthermore, Elai markedly reduced the recruitment of RORγ to its genomic DNA response element (RORE), suppressed the expression of RORγ target genes AR and AR variants, and significantly inhibited PCa cell growth. Importantly, Elai strongly suppressed tumor growth in both cell line based and patient-derived PCa xenograft models. Taken together, these results suggest that Elai is novel therapeutic RORγ inhibitor that can be used as a drug candidate for the treatment of human CRPC. Elsevier 2020-12 2020-07-12 /pmc/articles/PMC7745055/ /pubmed/33354503 http://dx.doi.org/10.1016/j.apsb.2020.07.001 Text en © 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Zheng, Jianwei
Wang, Junfeng
Wang, Qian
Zou, Hongye
Wang, Hong
Zhang, Zhenhua
Chen, Jianghe
Wang, Qianqian
Wang, Panxia
Zhao, Yueshan
Lu, Jing
Zhang, Xiaolei
Xiang, Songtao
Wang, Haibin
Lei, Jinping
Chen, Hong-Wu
Liu, Peiqing
Liu, Yonghong
Han, Fanghai
Wang, Junjian
Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title_full Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title_fullStr Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title_full_unstemmed Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title_short Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin
title_sort targeting castration-resistant prostate cancer with a novel rorγ antagonist elaiophylin
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745055/
https://www.ncbi.nlm.nih.gov/pubmed/33354503
http://dx.doi.org/10.1016/j.apsb.2020.07.001
work_keys_str_mv AT zhengjianwei targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wangjunfeng targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wangqian targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT zouhongye targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wanghong targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT zhangzhenhua targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT chenjianghe targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wangqianqian targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wangpanxia targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT zhaoyueshan targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT lujing targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT zhangxiaolei targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT xiangsongtao targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wanghaibin targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT leijinping targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT chenhongwu targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT liupeiqing targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT liuyonghong targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT hanfanghai targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin
AT wangjunjian targetingcastrationresistantprostatecancerwithanovelrorgantagonistelaiophylin