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A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()()
The high prevalence and long latency period of prostate cancer (PCa) provide a unique opportunity to control disease progression with dietary and nutraceutical approaches. We developed ProFine, a standardized composition of luteolin, quercetin, and kaempferol, and investigated its potential as a nut...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034581/ https://www.ncbi.nlm.nih.gov/pubmed/29981500 http://dx.doi.org/10.1016/j.neo.2018.06.003 |
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author | Mamouni, Kenza Zhang, Shumin Li, Xin Chen, Yanhua Yang, Yang Kim, Jaeah Bartlett, Michael G. Coleman, Ilsa M. Nelson, Peter S. Kucuk, Omer Wu, Daqing |
author_facet | Mamouni, Kenza Zhang, Shumin Li, Xin Chen, Yanhua Yang, Yang Kim, Jaeah Bartlett, Michael G. Coleman, Ilsa M. Nelson, Peter S. Kucuk, Omer Wu, Daqing |
author_sort | Mamouni, Kenza |
collection | PubMed |
description | The high prevalence and long latency period of prostate cancer (PCa) provide a unique opportunity to control disease progression with dietary and nutraceutical approaches. We developed ProFine, a standardized composition of luteolin, quercetin, and kaempferol, and investigated its potential as a nutraceutical for PCa in preclinical models. The three ingredients of ProFine demonstrated synergistic in vitro cytotoxicity and effectively induced apoptosis in PCa cells. ProFine markedly affected the transcriptome of PCa cells, suppressed the expression of androgen receptor, and inhibited androgen-regulated genes. Oral administration of ProFine did not exhibit obvious toxicities in mice, and the three ingredients retained their individual pharmacokinetic and bioavailability profiles. Importantly, ProFine significantly retarded the growth of PCa xenografts in athymic nude mice and extended the survival of animals. This study provides preclinical evidence supporting the promise of ProFine as a safe, efficacious, and affordable intervention to control PCa progression and improve clinical outcomes. |
format | Online Article Text |
id | pubmed-6034581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60345812018-07-10 A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() Mamouni, Kenza Zhang, Shumin Li, Xin Chen, Yanhua Yang, Yang Kim, Jaeah Bartlett, Michael G. Coleman, Ilsa M. Nelson, Peter S. Kucuk, Omer Wu, Daqing Neoplasia Original article The high prevalence and long latency period of prostate cancer (PCa) provide a unique opportunity to control disease progression with dietary and nutraceutical approaches. We developed ProFine, a standardized composition of luteolin, quercetin, and kaempferol, and investigated its potential as a nutraceutical for PCa in preclinical models. The three ingredients of ProFine demonstrated synergistic in vitro cytotoxicity and effectively induced apoptosis in PCa cells. ProFine markedly affected the transcriptome of PCa cells, suppressed the expression of androgen receptor, and inhibited androgen-regulated genes. Oral administration of ProFine did not exhibit obvious toxicities in mice, and the three ingredients retained their individual pharmacokinetic and bioavailability profiles. Importantly, ProFine significantly retarded the growth of PCa xenografts in athymic nude mice and extended the survival of animals. This study provides preclinical evidence supporting the promise of ProFine as a safe, efficacious, and affordable intervention to control PCa progression and improve clinical outcomes. Neoplasia Press 2018-07-04 /pmc/articles/PMC6034581/ /pubmed/29981500 http://dx.doi.org/10.1016/j.neo.2018.06.003 Text en © 2018 The Authors 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 Mamouni, Kenza Zhang, Shumin Li, Xin Chen, Yanhua Yang, Yang Kim, Jaeah Bartlett, Michael G. Coleman, Ilsa M. Nelson, Peter S. Kucuk, Omer Wu, Daqing A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title | A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title_full | A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title_fullStr | A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title_full_unstemmed | A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title_short | A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models()() |
title_sort | novel flavonoid composition targets androgen receptor signaling and inhibits prostate cancer growth in preclinical models()() |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034581/ https://www.ncbi.nlm.nih.gov/pubmed/29981500 http://dx.doi.org/10.1016/j.neo.2018.06.003 |
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