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Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN

Prostate cancer is a form of cancer that develops in the prostate, a gland in the male reproductive system. In the present study, the activation of the farnesoid X receptor (FXR), a member of the nuclear receptor superfamily, was demonstrated to inhibit cell proliferation in LNcaP cells. Using clini...

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Autores principales: LIU, JUN, TONG, SHI-JUN, WANG, XIANG, QU, LIAN-XI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151690/
https://www.ncbi.nlm.nih.gov/pubmed/25187826
http://dx.doi.org/10.3892/etm.2014.1894
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author LIU, JUN
TONG, SHI-JUN
WANG, XIANG
QU, LIAN-XI
author_facet LIU, JUN
TONG, SHI-JUN
WANG, XIANG
QU, LIAN-XI
author_sort LIU, JUN
collection PubMed
description Prostate cancer is a form of cancer that develops in the prostate, a gland in the male reproductive system. In the present study, the activation of the farnesoid X receptor (FXR), a member of the nuclear receptor superfamily, was demonstrated to inhibit cell proliferation in LNcaP cells. Using clinical samples, mRNA and protein levels of FXR were found to be significantly decreased by quantitative PCR and western blot analysis in prostate cancer tissues. In vitro studies identified further that activation or overexpression of FXR suppressed prostate cancer cell proliferation as measured by BrdU incorporation assays. At the molecular level, the results further revealed that the expression of the tumor suppressor gene, PTEN, was upregulated by FXR activation. Therefore, the observations indicated that FXR functions as a tumor suppressor in prostate cancer, which may provide a novel method for molecular targeting cancer treatment.
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spelling pubmed-41516902014-09-03 Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN LIU, JUN TONG, SHI-JUN WANG, XIANG QU, LIAN-XI Exp Ther Med Articles Prostate cancer is a form of cancer that develops in the prostate, a gland in the male reproductive system. In the present study, the activation of the farnesoid X receptor (FXR), a member of the nuclear receptor superfamily, was demonstrated to inhibit cell proliferation in LNcaP cells. Using clinical samples, mRNA and protein levels of FXR were found to be significantly decreased by quantitative PCR and western blot analysis in prostate cancer tissues. In vitro studies identified further that activation or overexpression of FXR suppressed prostate cancer cell proliferation as measured by BrdU incorporation assays. At the molecular level, the results further revealed that the expression of the tumor suppressor gene, PTEN, was upregulated by FXR activation. Therefore, the observations indicated that FXR functions as a tumor suppressor in prostate cancer, which may provide a novel method for molecular targeting cancer treatment. D.A. Spandidos 2014-10 2014-08-11 /pmc/articles/PMC4151690/ /pubmed/25187826 http://dx.doi.org/10.3892/etm.2014.1894 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
LIU, JUN
TONG, SHI-JUN
WANG, XIANG
QU, LIAN-XI
Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title_full Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title_fullStr Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title_full_unstemmed Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title_short Farnesoid X receptor inhibits LNcaP cell proliferation via the upregulation of PTEN
title_sort farnesoid x receptor inhibits lncap cell proliferation via the upregulation of pten
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151690/
https://www.ncbi.nlm.nih.gov/pubmed/25187826
http://dx.doi.org/10.3892/etm.2014.1894
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