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Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex
Ciclopirox (CPX) is an FDA-approved topical antifungal agent that has demonstrated preclinical anticancer activity in a number of solid and hematologic malignancies. Its clinical utility as an oral anticancer agent, however, is limited by poor oral bioavailability and gastrointestinal toxicity. Fosc...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166826/ https://www.ncbi.nlm.nih.gov/pubmed/34059639 http://dx.doi.org/10.1038/s41419-021-03836-z |
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author | Weir, Scott J. Dandawate, Prasad Standing, David Bhattacharyya, Sangita Ramamoorthy, Prabhu Rangarajan, Parthasarathy Wood, Robyn Brinker, Amanda E. Woolbright, Benjamin L. Tanol, Mehmet Ham, Tammy McCulloch, William Dalton, Michael Reed, Gregory A. Baltezor, Michael J. Jensen, Roy A. Taylor, John A. Anant, Shrikant |
author_facet | Weir, Scott J. Dandawate, Prasad Standing, David Bhattacharyya, Sangita Ramamoorthy, Prabhu Rangarajan, Parthasarathy Wood, Robyn Brinker, Amanda E. Woolbright, Benjamin L. Tanol, Mehmet Ham, Tammy McCulloch, William Dalton, Michael Reed, Gregory A. Baltezor, Michael J. Jensen, Roy A. Taylor, John A. Anant, Shrikant |
author_sort | Weir, Scott J. |
collection | PubMed |
description | Ciclopirox (CPX) is an FDA-approved topical antifungal agent that has demonstrated preclinical anticancer activity in a number of solid and hematologic malignancies. Its clinical utility as an oral anticancer agent, however, is limited by poor oral bioavailability and gastrointestinal toxicity. Fosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration. We characterized the activity of CPX-POM and its major metabolites in in vitro and in vivo preclinical models of high-grade urothelial cancer. CPX inhibited cell proliferation, clonogenicity and spheroid formation, and increased cell cycle arrest at S and G0/G1 phases. Mechanistically, CPX suppressed activation of Notch signaling. Molecular modeling and cellular thermal shift assays demonstrated CPX binding to γ-secretase complex proteins Presenilin 1 and Nicastrin, which are essential for Notch activation. To establish in vivo preclinical proof of principle, we tested fosciclopirox in the validated N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) mouse bladder cancer model. Once-daily intraperitoneal administration of CPX-POM for four weeks at doses of 235 mg/kg and 470 mg/kg significantly decreased bladder weight, a surrogate for tumor volume, and resulted in a migration to lower stage tumors in CPX-POM treated animals. This was coupled with a reduction in the proliferation index. Additionally, there was a reduction in Presenilin 1 and Hes-1 expression in the bladder tissues of CPX-POM treated animals. Following the completion of the first-in-human Phase 1 trial (NCT03348514), the pharmacologic activity of fosciclopirox is currently being characterized in a Phase 1 expansion cohort study of muscle-invasive bladder cancer patients scheduled for cystectomy (NCT04608045) as well as a Phase 2 trial of newly diagnosed and recurrent urothelial cancer patients scheduled for transurethral resection of bladder tumors (NCT04525131). |
format | Online Article Text |
id | pubmed-8166826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81668262021-06-15 Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex Weir, Scott J. Dandawate, Prasad Standing, David Bhattacharyya, Sangita Ramamoorthy, Prabhu Rangarajan, Parthasarathy Wood, Robyn Brinker, Amanda E. Woolbright, Benjamin L. Tanol, Mehmet Ham, Tammy McCulloch, William Dalton, Michael Reed, Gregory A. Baltezor, Michael J. Jensen, Roy A. Taylor, John A. Anant, Shrikant Cell Death Dis Article Ciclopirox (CPX) is an FDA-approved topical antifungal agent that has demonstrated preclinical anticancer activity in a number of solid and hematologic malignancies. Its clinical utility as an oral anticancer agent, however, is limited by poor oral bioavailability and gastrointestinal toxicity. Fosciclopirox, the phosphoryloxymethyl ester of CPX (Ciclopirox Prodrug, CPX-POM), selectively delivers the active metabolite, CPX, to the entire urinary tract following parenteral administration. We characterized the activity of CPX-POM and its major metabolites in in vitro and in vivo preclinical models of high-grade urothelial cancer. CPX inhibited cell proliferation, clonogenicity and spheroid formation, and increased cell cycle arrest at S and G0/G1 phases. Mechanistically, CPX suppressed activation of Notch signaling. Molecular modeling and cellular thermal shift assays demonstrated CPX binding to γ-secretase complex proteins Presenilin 1 and Nicastrin, which are essential for Notch activation. To establish in vivo preclinical proof of principle, we tested fosciclopirox in the validated N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN) mouse bladder cancer model. Once-daily intraperitoneal administration of CPX-POM for four weeks at doses of 235 mg/kg and 470 mg/kg significantly decreased bladder weight, a surrogate for tumor volume, and resulted in a migration to lower stage tumors in CPX-POM treated animals. This was coupled with a reduction in the proliferation index. Additionally, there was a reduction in Presenilin 1 and Hes-1 expression in the bladder tissues of CPX-POM treated animals. Following the completion of the first-in-human Phase 1 trial (NCT03348514), the pharmacologic activity of fosciclopirox is currently being characterized in a Phase 1 expansion cohort study of muscle-invasive bladder cancer patients scheduled for cystectomy (NCT04608045) as well as a Phase 2 trial of newly diagnosed and recurrent urothelial cancer patients scheduled for transurethral resection of bladder tumors (NCT04525131). Nature Publishing Group UK 2021-05-31 /pmc/articles/PMC8166826/ /pubmed/34059639 http://dx.doi.org/10.1038/s41419-021-03836-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Weir, Scott J. Dandawate, Prasad Standing, David Bhattacharyya, Sangita Ramamoorthy, Prabhu Rangarajan, Parthasarathy Wood, Robyn Brinker, Amanda E. Woolbright, Benjamin L. Tanol, Mehmet Ham, Tammy McCulloch, William Dalton, Michael Reed, Gregory A. Baltezor, Michael J. Jensen, Roy A. Taylor, John A. Anant, Shrikant Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title | Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title_full | Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title_fullStr | Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title_full_unstemmed | Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title_short | Fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
title_sort | fosciclopirox suppresses growth of high-grade urothelial cancer by targeting the γ-secretase complex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166826/ https://www.ncbi.nlm.nih.gov/pubmed/34059639 http://dx.doi.org/10.1038/s41419-021-03836-z |
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