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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),...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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 |
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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 |
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