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A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells
Carcinoma progression is associated with the loss of epithelial features and the acquisition of a mesenchymal phenotype, a process known as epithelial-mesenchymal transition (EMT). Resveratrol, a natural polyphenolic compound found in grapes, berries and peanuts, has a wide range of pharmacological...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148361/ https://www.ncbi.nlm.nih.gov/pubmed/25069516 http://dx.doi.org/10.3892/mmr.2014.2417 |
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author | LI, JIANPING CHONG, TIE WANG, ZIMING CHEN, HAIWEN LI, HECHENG CAO, JUN ZHANG, PENG LI, HONGLIANG |
author_facet | LI, JIANPING CHONG, TIE WANG, ZIMING CHEN, HAIWEN LI, HECHENG CAO, JUN ZHANG, PENG LI, HONGLIANG |
author_sort | LI, JIANPING |
collection | PubMed |
description | Carcinoma progression is associated with the loss of epithelial features and the acquisition of a mesenchymal phenotype, a process known as epithelial-mesenchymal transition (EMT). Resveratrol, a natural polyphenolic compound found in grapes, berries and peanuts, has a wide range of pharmacological properties, including anti-tumor metastasis properties. The underlying mechanism through which resveratrol inhibits metastasis of prostate cancer (PCa) is not yet fully understood; however, it is thought to be associated with the disruption of EMT. In the present study, lipopolysaccharide (LPS) was used to trigger EMT in PC-3 and LNCaP PCa cell lines, and the cell lines were subsequently treated with resveratrol. The results demonstrated that exposure of PC-3 and LNCaP cells to LPS resulted in morphological alterations characteristic of EMT, as well as an increase in the expression of the mesenchymal marker vimentin and a decrease in the expression of E-cadherin. In addition, LPS exposure resulted in an increase in cell motility, along with an upregulation of the transcription factor glioma-associated oncogene homolog 1 (Gli1). However, treatment with resveratrol inhibited LPS-induced morphological changes, decreased the expression of LPS-induced markers of EMT and inhibited the expression of Gli1, resulting in the inhibition of in vitro cell motility and invasiveness. These results provide a novel perspective for the anti-invasion mechanism of resveratrol, suggesting that the effect is in part due to its ability to inhibit the EMT process through the Hedgehog signaling pathway. |
format | Online Article Text |
id | pubmed-4148361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-41483612014-08-29 A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells LI, JIANPING CHONG, TIE WANG, ZIMING CHEN, HAIWEN LI, HECHENG CAO, JUN ZHANG, PENG LI, HONGLIANG Mol Med Rep Articles Carcinoma progression is associated with the loss of epithelial features and the acquisition of a mesenchymal phenotype, a process known as epithelial-mesenchymal transition (EMT). Resveratrol, a natural polyphenolic compound found in grapes, berries and peanuts, has a wide range of pharmacological properties, including anti-tumor metastasis properties. The underlying mechanism through which resveratrol inhibits metastasis of prostate cancer (PCa) is not yet fully understood; however, it is thought to be associated with the disruption of EMT. In the present study, lipopolysaccharide (LPS) was used to trigger EMT in PC-3 and LNCaP PCa cell lines, and the cell lines were subsequently treated with resveratrol. The results demonstrated that exposure of PC-3 and LNCaP cells to LPS resulted in morphological alterations characteristic of EMT, as well as an increase in the expression of the mesenchymal marker vimentin and a decrease in the expression of E-cadherin. In addition, LPS exposure resulted in an increase in cell motility, along with an upregulation of the transcription factor glioma-associated oncogene homolog 1 (Gli1). However, treatment with resveratrol inhibited LPS-induced morphological changes, decreased the expression of LPS-induced markers of EMT and inhibited the expression of Gli1, resulting in the inhibition of in vitro cell motility and invasiveness. These results provide a novel perspective for the anti-invasion mechanism of resveratrol, suggesting that the effect is in part due to its ability to inhibit the EMT process through the Hedgehog signaling pathway. D.A. Spandidos 2014-10 2014-07-23 /pmc/articles/PMC4148361/ /pubmed/25069516 http://dx.doi.org/10.3892/mmr.2014.2417 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles LI, JIANPING CHONG, TIE WANG, ZIMING CHEN, HAIWEN LI, HECHENG CAO, JUN ZHANG, PENG LI, HONGLIANG A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title | A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title_full | A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title_fullStr | A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title_full_unstemmed | A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title_short | A novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
title_sort | novel anti-cancer effect of resveratrol: reversal of epithelial-mesenchymal transition in prostate cancer cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148361/ https://www.ncbi.nlm.nih.gov/pubmed/25069516 http://dx.doi.org/10.3892/mmr.2014.2417 |
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