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Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential

Recently, many studies have indicated that ambient air particulate matter (PM) can increase the risk of oral cancer. The most common malignant tumor in the oral cavity is oral squamous cell carcinoma (OSCC). Usually, cancer cell migration/invasion is the most important cause of cancer mortality. Mat...

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Autores principales: Vo, Thi Thuy Tien, Lee, Chiang-Wen, Wu, Ching-Zong, Liu, Ju-Fang, Lin, Wei-Ning, Chen, Yuh-Lien, Hsu, Lee-Fen, Tsai, Ming-Horng, Lee, I-Ta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477423/
https://www.ncbi.nlm.nih.gov/pubmed/32922544
http://dx.doi.org/10.7150/jca.48296
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author Vo, Thi Thuy Tien
Lee, Chiang-Wen
Wu, Ching-Zong
Liu, Ju-Fang
Lin, Wei-Ning
Chen, Yuh-Lien
Hsu, Lee-Fen
Tsai, Ming-Horng
Lee, I-Ta
author_facet Vo, Thi Thuy Tien
Lee, Chiang-Wen
Wu, Ching-Zong
Liu, Ju-Fang
Lin, Wei-Ning
Chen, Yuh-Lien
Hsu, Lee-Fen
Tsai, Ming-Horng
Lee, I-Ta
author_sort Vo, Thi Thuy Tien
collection PubMed
description Recently, many studies have indicated that ambient air particulate matter (PM) can increase the risk of oral cancer. The most common malignant tumor in the oral cavity is oral squamous cell carcinoma (OSCC). Usually, cancer cell migration/invasion is the most important cause of cancer mortality. Matrix metalloproteinase-2 (MMP-2) and MMP-9 have been shown to play important roles in regulating metastasis and the tumor microenvironment. Here, we studied the anti-cancer effects of surfactin, a cyclic lipopeptide generated by Bacillus subtilis, on cancer cell migration and invasion. Surfactin suppressed PM-promoted cell migration and invasion and colony formation of SCC4 and SCC25 human oral squamous cell carcinoma cell lines. We observed that PM induced MMP-2 and MMP-9 expression, which was inhibited by surfactin. Transfection with p65, p50, c-Jun, c-Fos, p85, p110, Akt, mammalian target of rapamycin (mTOR), or interleukin-6 (IL-6) siRNA markedly inhibited PM-induced MMP-2 and MMP-9 expression. Moreover, surfactin could reduce Akt, mTOR, p65, and c-Jun activation and IL-6 secretion induced by PM. Finally, we proved that transfection with Akt, p65, or c-Jun siRNA significantly inhibited PM-induced IL-6 release. Taken together, these results suggest that surfactin functions as a suppressor of PM-induced MMP2/9-dependent oral cancer cell migration and invasion by inhibiting the activation of phosphoinositide 3-kinase (PI3K)/Akt/mTOR and PI3K/Akt/nuclear factor-κB (NF-κB) and activator protein-1 (AP-1)/IL-6 signaling pathways.
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spelling pubmed-74774232020-09-11 Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential Vo, Thi Thuy Tien Lee, Chiang-Wen Wu, Ching-Zong Liu, Ju-Fang Lin, Wei-Ning Chen, Yuh-Lien Hsu, Lee-Fen Tsai, Ming-Horng Lee, I-Ta J Cancer Research Paper Recently, many studies have indicated that ambient air particulate matter (PM) can increase the risk of oral cancer. The most common malignant tumor in the oral cavity is oral squamous cell carcinoma (OSCC). Usually, cancer cell migration/invasion is the most important cause of cancer mortality. Matrix metalloproteinase-2 (MMP-2) and MMP-9 have been shown to play important roles in regulating metastasis and the tumor microenvironment. Here, we studied the anti-cancer effects of surfactin, a cyclic lipopeptide generated by Bacillus subtilis, on cancer cell migration and invasion. Surfactin suppressed PM-promoted cell migration and invasion and colony formation of SCC4 and SCC25 human oral squamous cell carcinoma cell lines. We observed that PM induced MMP-2 and MMP-9 expression, which was inhibited by surfactin. Transfection with p65, p50, c-Jun, c-Fos, p85, p110, Akt, mammalian target of rapamycin (mTOR), or interleukin-6 (IL-6) siRNA markedly inhibited PM-induced MMP-2 and MMP-9 expression. Moreover, surfactin could reduce Akt, mTOR, p65, and c-Jun activation and IL-6 secretion induced by PM. Finally, we proved that transfection with Akt, p65, or c-Jun siRNA significantly inhibited PM-induced IL-6 release. Taken together, these results suggest that surfactin functions as a suppressor of PM-induced MMP2/9-dependent oral cancer cell migration and invasion by inhibiting the activation of phosphoinositide 3-kinase (PI3K)/Akt/mTOR and PI3K/Akt/nuclear factor-κB (NF-κB) and activator protein-1 (AP-1)/IL-6 signaling pathways. Ivyspring International Publisher 2020-08-18 /pmc/articles/PMC7477423/ /pubmed/32922544 http://dx.doi.org/10.7150/jca.48296 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Vo, Thi Thuy Tien
Lee, Chiang-Wen
Wu, Ching-Zong
Liu, Ju-Fang
Lin, Wei-Ning
Chen, Yuh-Lien
Hsu, Lee-Fen
Tsai, Ming-Horng
Lee, I-Ta
Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title_full Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title_fullStr Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title_full_unstemmed Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title_short Surfactin from Bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
title_sort surfactin from bacillus subtilis attenuates ambient air particulate matter-promoted human oral cancer cells metastatic potential
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477423/
https://www.ncbi.nlm.nih.gov/pubmed/32922544
http://dx.doi.org/10.7150/jca.48296
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