Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: LI, JIANPING, CHONG, TIE, WANG, ZIMING, CHEN, HAIWEN, LI, HECHENG, CAO, JUN, ZHANG, PENG, LI, HONGLIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
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
_version_ 1782332611075506176
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
work_keys_str_mv AT lijianping anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT chongtie anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT wangziming anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT chenhaiwen anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT lihecheng anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT caojun anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT zhangpeng anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT lihongliang anovelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT lijianping novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT chongtie novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT wangziming novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT chenhaiwen novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT lihecheng novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT caojun novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT zhangpeng novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells
AT lihongliang novelanticancereffectofresveratrolreversalofepithelialmesenchymaltransitioninprostatecancercells