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MAPK/P53-mediated FASN expression in bone tumors

The correlation between mitogen-activated protein kinase (MAPK)/P53 signaling-dependent fatty acid synthase (FASN) expression and bone tumors was examined in the present study. We established the SH081 bone tumor cell line, which was used to determine the expression of FASN and MAPK/P53 at the mRNA...

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Autores principales: Jiang, Ye, Yin, Xiaofan, Wu, Liang, Qin, Qiang, Xu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452927/
https://www.ncbi.nlm.nih.gov/pubmed/28588696
http://dx.doi.org/10.3892/ol.2017.6015
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author Jiang, Ye
Yin, Xiaofan
Wu, Liang
Qin, Qiang
Xu, Jun
author_facet Jiang, Ye
Yin, Xiaofan
Wu, Liang
Qin, Qiang
Xu, Jun
author_sort Jiang, Ye
collection PubMed
description The correlation between mitogen-activated protein kinase (MAPK)/P53 signaling-dependent fatty acid synthase (FASN) expression and bone tumors was examined in the present study. We established the SH081 bone tumor cell line, which was used to determine the expression of FASN and MAPK/P53 at the mRNA and protein levels in bone tumor cells and normal cells. Compared with the normal cells, the expression of MAPK/P53 and FASN mRNA was significantly elevated, whereas inhibition of MAPK/P53 decreased FASN expression. Similarly, the expression of FASN and MAPK/P53 proteins were significantly elevated in the bone tumor cells and treatment with the MAPK/P53 inhibitor decreased the expression of FASN. To determine the role of MAPK/P53 in cell proliferation, bone cancer cells were treated with MAPK/P53 inhibitor and the results showed a reduced proliferation rate. Thus, FASN promotes the development of bone tumors and MAPK/P53 signaling contributes to bone tumors by upregulating the expression of FASN.
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spelling pubmed-54529272017-06-06 MAPK/P53-mediated FASN expression in bone tumors Jiang, Ye Yin, Xiaofan Wu, Liang Qin, Qiang Xu, Jun Oncol Lett Articles The correlation between mitogen-activated protein kinase (MAPK)/P53 signaling-dependent fatty acid synthase (FASN) expression and bone tumors was examined in the present study. We established the SH081 bone tumor cell line, which was used to determine the expression of FASN and MAPK/P53 at the mRNA and protein levels in bone tumor cells and normal cells. Compared with the normal cells, the expression of MAPK/P53 and FASN mRNA was significantly elevated, whereas inhibition of MAPK/P53 decreased FASN expression. Similarly, the expression of FASN and MAPK/P53 proteins were significantly elevated in the bone tumor cells and treatment with the MAPK/P53 inhibitor decreased the expression of FASN. To determine the role of MAPK/P53 in cell proliferation, bone cancer cells were treated with MAPK/P53 inhibitor and the results showed a reduced proliferation rate. Thus, FASN promotes the development of bone tumors and MAPK/P53 signaling contributes to bone tumors by upregulating the expression of FASN. D.A. Spandidos 2017-06 2017-04-10 /pmc/articles/PMC5452927/ /pubmed/28588696 http://dx.doi.org/10.3892/ol.2017.6015 Text en Copyright: © Jiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Jiang, Ye
Yin, Xiaofan
Wu, Liang
Qin, Qiang
Xu, Jun
MAPK/P53-mediated FASN expression in bone tumors
title MAPK/P53-mediated FASN expression in bone tumors
title_full MAPK/P53-mediated FASN expression in bone tumors
title_fullStr MAPK/P53-mediated FASN expression in bone tumors
title_full_unstemmed MAPK/P53-mediated FASN expression in bone tumors
title_short MAPK/P53-mediated FASN expression in bone tumors
title_sort mapk/p53-mediated fasn expression in bone tumors
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452927/
https://www.ncbi.nlm.nih.gov/pubmed/28588696
http://dx.doi.org/10.3892/ol.2017.6015
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