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Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction
Toluene diisocyanate (TDI) is commonly used in manufacturing, and it is highly reactive and causes respiratory damage. This study aims to identify the mechanism of tumorigenesis in bronchial epithelial cells induced by chronic TDI exposure. In addition, transcriptome analysis results confirmed that...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093867/ https://www.ncbi.nlm.nih.gov/pubmed/37047129 http://dx.doi.org/10.3390/ijms24076157 |
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author | Han, Dong-Hee Shin, Min Kyoung Oh, Jin Wook Lee, Junha Sung, Jung-Suk Kim, Min |
author_facet | Han, Dong-Hee Shin, Min Kyoung Oh, Jin Wook Lee, Junha Sung, Jung-Suk Kim, Min |
author_sort | Han, Dong-Hee |
collection | PubMed |
description | Toluene diisocyanate (TDI) is commonly used in manufacturing, and it is highly reactive and causes respiratory damage. This study aims to identify the mechanism of tumorigenesis in bronchial epithelial cells induced by chronic TDI exposure. In addition, transcriptome analysis results confirmed that TDI increases transforming growth factor-beta 1 (TGF-β1) expression and regulates genes associated with cancerous characteristics in bronchial cells. Our chronically TDI-exposed model exhibited elongated spindle-like morphology, a mesenchymal characteristic. Epithelial-mesenchymal transition (EMT) was evaluated following chronic TDI exposure, and EMT biomarkers increased concentration-dependently. Furthermore, our results indicated diminished cell adhesion molecules and intensified cell migration and invasion. In order to investigate the cellular regulatory mechanisms resulting from chronic TDI exposure, we focused on TGF-β1, a key factor regulated by TDI exposure. As predicted, TGF-β1 was significantly up-regulated and secreted in chronically TDI-exposed cells. In addition, SMAD2/3 was also activated considerably as it is the direct target of TGF-β1 and TGF-β1 receptors. Inhibiting TGF-β1 signaling through blocking of the TGF-β receptor attenuated EMT and cell migration in chronically TDI-exposed cells. Our results corroborate that chronic TDI exposure upregulates TGF-β1 secretion, activates TGF-β1 signal transduction, and leads to EMT and other cancer properties. |
format | Online Article Text |
id | pubmed-10093867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100938672023-04-13 Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction Han, Dong-Hee Shin, Min Kyoung Oh, Jin Wook Lee, Junha Sung, Jung-Suk Kim, Min Int J Mol Sci Article Toluene diisocyanate (TDI) is commonly used in manufacturing, and it is highly reactive and causes respiratory damage. This study aims to identify the mechanism of tumorigenesis in bronchial epithelial cells induced by chronic TDI exposure. In addition, transcriptome analysis results confirmed that TDI increases transforming growth factor-beta 1 (TGF-β1) expression and regulates genes associated with cancerous characteristics in bronchial cells. Our chronically TDI-exposed model exhibited elongated spindle-like morphology, a mesenchymal characteristic. Epithelial-mesenchymal transition (EMT) was evaluated following chronic TDI exposure, and EMT biomarkers increased concentration-dependently. Furthermore, our results indicated diminished cell adhesion molecules and intensified cell migration and invasion. In order to investigate the cellular regulatory mechanisms resulting from chronic TDI exposure, we focused on TGF-β1, a key factor regulated by TDI exposure. As predicted, TGF-β1 was significantly up-regulated and secreted in chronically TDI-exposed cells. In addition, SMAD2/3 was also activated considerably as it is the direct target of TGF-β1 and TGF-β1 receptors. Inhibiting TGF-β1 signaling through blocking of the TGF-β receptor attenuated EMT and cell migration in chronically TDI-exposed cells. Our results corroborate that chronic TDI exposure upregulates TGF-β1 secretion, activates TGF-β1 signal transduction, and leads to EMT and other cancer properties. MDPI 2023-03-24 /pmc/articles/PMC10093867/ /pubmed/37047129 http://dx.doi.org/10.3390/ijms24076157 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Han, Dong-Hee Shin, Min Kyoung Oh, Jin Wook Lee, Junha Sung, Jung-Suk Kim, Min Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title | Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title_full | Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title_fullStr | Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title_full_unstemmed | Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title_short | Chronic Exposure to TDI Induces Cell Migration and Invasion via TGF-β1 Signal Transduction |
title_sort | chronic exposure to tdi induces cell migration and invasion via tgf-β1 signal transduction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093867/ https://www.ncbi.nlm.nih.gov/pubmed/37047129 http://dx.doi.org/10.3390/ijms24076157 |
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