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Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro

Epithelial-mesenchymal transition (EMT) is potentially involved in increasing metastasis of oral squamous cell carcinoma (OSCC). Periodontal pathogens are well-known for their ability to induce intense immune responses and here we investigated whether they are involved in inducing EMT. Cultures of O...

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Autores principales: Abdulkareem, A. A., Shelton, R. M., Landini, G., Cooper, P. R., Milward, M. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927641/
https://www.ncbi.nlm.nih.gov/pubmed/28873015
http://dx.doi.org/10.1080/19336918.2017.1322253
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author Abdulkareem, A. A.
Shelton, R. M.
Landini, G.
Cooper, P. R.
Milward, M. R.
author_facet Abdulkareem, A. A.
Shelton, R. M.
Landini, G.
Cooper, P. R.
Milward, M. R.
author_sort Abdulkareem, A. A.
collection PubMed
description Epithelial-mesenchymal transition (EMT) is potentially involved in increasing metastasis of oral squamous cell carcinoma (OSCC). Periodontal pathogens are well-known for their ability to induce intense immune responses and here we investigated whether they are involved in inducing EMT. Cultures of OSCC cell line (H400) were treated separately with heat-killed periodontal pathogens F. nucleatum, or P. gingivalis or E. coli LPS for 8 d. EMT-associated features were assayed using sq-PCR and PCR-arrays, for EMT-related markers, and ELISAs for TGF-β1, TNF-α, and EGF. The migratory ability of cells was investigated using scratch and transwell migration assays. E-cadherin and vimentin expression was assessed using immunofluorescence while Snail activation was detected with immunocytochemistry. In addition, the integrity of the cultured epithelial layer was investigated using transepithelial electrical resistance (TEER). PCR data showed significant upregulation after 1, 5, and 8 d in transcription of mesenchymal markers and downregulation of epithelial ones compared with unstimulated controls, which were confirmed by immunofluorescence. Periodontal pathogens also caused a significant increase in level of all cytokines investigated which could be involved in EMT-induction and Snail activation. Exposure of cells to the bacteria increased migration and the rate of wound closure. Downregulation of epithelial markers also resulted in a significant decrease in impedance resistance of cell monolayers to passage of electrical current. These results suggested that EMT was likely induced in OSCC cells in response to stimulation by periodontal pathogens.
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spelling pubmed-59276412018-05-02 Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro Abdulkareem, A. A. Shelton, R. M. Landini, G. Cooper, P. R. Milward, M. R. Cell Adh Migr Research Paper Epithelial-mesenchymal transition (EMT) is potentially involved in increasing metastasis of oral squamous cell carcinoma (OSCC). Periodontal pathogens are well-known for their ability to induce intense immune responses and here we investigated whether they are involved in inducing EMT. Cultures of OSCC cell line (H400) were treated separately with heat-killed periodontal pathogens F. nucleatum, or P. gingivalis or E. coli LPS for 8 d. EMT-associated features were assayed using sq-PCR and PCR-arrays, for EMT-related markers, and ELISAs for TGF-β1, TNF-α, and EGF. The migratory ability of cells was investigated using scratch and transwell migration assays. E-cadherin and vimentin expression was assessed using immunofluorescence while Snail activation was detected with immunocytochemistry. In addition, the integrity of the cultured epithelial layer was investigated using transepithelial electrical resistance (TEER). PCR data showed significant upregulation after 1, 5, and 8 d in transcription of mesenchymal markers and downregulation of epithelial ones compared with unstimulated controls, which were confirmed by immunofluorescence. Periodontal pathogens also caused a significant increase in level of all cytokines investigated which could be involved in EMT-induction and Snail activation. Exposure of cells to the bacteria increased migration and the rate of wound closure. Downregulation of epithelial markers also resulted in a significant decrease in impedance resistance of cell monolayers to passage of electrical current. These results suggested that EMT was likely induced in OSCC cells in response to stimulation by periodontal pathogens. Taylor & Francis 2017-09-12 /pmc/articles/PMC5927641/ /pubmed/28873015 http://dx.doi.org/10.1080/19336918.2017.1322253 Text en © 2017 The Author(s). Published with license by Taylor & Francis. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Abdulkareem, A. A.
Shelton, R. M.
Landini, G.
Cooper, P. R.
Milward, M. R.
Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title_full Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title_fullStr Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title_full_unstemmed Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title_short Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
title_sort periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5927641/
https://www.ncbi.nlm.nih.gov/pubmed/28873015
http://dx.doi.org/10.1080/19336918.2017.1322253
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