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Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol
Rab coupling protein (RCP) is upregulated in head and neck squamous cell carcinoma (HNSCC) and is correlated with the progression and survival of patients. However, the role of RCP in one of the aggressive types of HNSCC, oral squamous cell carcinoma (OSCC), remains elusive. In the present study, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080807/ https://www.ncbi.nlm.nih.gov/pubmed/32728068 http://dx.doi.org/10.1038/s12276-020-0474-1 |
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author | Kim, Jin Young Cho, Kyung Hwa Jeong, Bo Young Park, Chang Gyo Lee, Hoi Young |
author_facet | Kim, Jin Young Cho, Kyung Hwa Jeong, Bo Young Park, Chang Gyo Lee, Hoi Young |
author_sort | Kim, Jin Young |
collection | PubMed |
description | Rab coupling protein (RCP) is upregulated in head and neck squamous cell carcinoma (HNSCC) and is correlated with the progression and survival of patients. However, the role of RCP in one of the aggressive types of HNSCC, oral squamous cell carcinoma (OSCC), remains elusive. In the present study, we identified the important role of Zeb1 in RCP-induced OSCC epithelial-to-mesenchymal transition (EMT) and invasion. RCP induces Zeb1 expression, and silencing Zeb1 expression significantly inhibits RCP-induced OSCC invasion. In addition, Zeb1 upregulates MT1-MMP expression to promote OSCC EMT and invasion. Furthermore, we observed that the β1 integrin/EGFR/β-catenin signaling cascade mediates RCP-induced Zeb1 expression to promote OSCC invasion. Notably, we provide evidence that resveratrol (REV) strongly inhibits RCP-induced Zeb1 expression through blocking β1 integrin endosome recycling and EGFR activation, leading to suppression of RCP-induced OSCC invasion, demonstrating the important role of RCP in OSCC invasion and its reversion by REV. Collectively, the present study provides evidence for the first time that RCP aggravates OSCC invasion through increasing Zeb1 expression and subsequently upregulating MT1-MMP expression and that this process is reversed by REV, providing novel biomarkers and indicating the therapeutic potential of REV in OSCC. |
format | Online Article Text |
id | pubmed-8080807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80808072021-04-29 Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol Kim, Jin Young Cho, Kyung Hwa Jeong, Bo Young Park, Chang Gyo Lee, Hoi Young Exp Mol Med Article Rab coupling protein (RCP) is upregulated in head and neck squamous cell carcinoma (HNSCC) and is correlated with the progression and survival of patients. However, the role of RCP in one of the aggressive types of HNSCC, oral squamous cell carcinoma (OSCC), remains elusive. In the present study, we identified the important role of Zeb1 in RCP-induced OSCC epithelial-to-mesenchymal transition (EMT) and invasion. RCP induces Zeb1 expression, and silencing Zeb1 expression significantly inhibits RCP-induced OSCC invasion. In addition, Zeb1 upregulates MT1-MMP expression to promote OSCC EMT and invasion. Furthermore, we observed that the β1 integrin/EGFR/β-catenin signaling cascade mediates RCP-induced Zeb1 expression to promote OSCC invasion. Notably, we provide evidence that resveratrol (REV) strongly inhibits RCP-induced Zeb1 expression through blocking β1 integrin endosome recycling and EGFR activation, leading to suppression of RCP-induced OSCC invasion, demonstrating the important role of RCP in OSCC invasion and its reversion by REV. Collectively, the present study provides evidence for the first time that RCP aggravates OSCC invasion through increasing Zeb1 expression and subsequently upregulating MT1-MMP expression and that this process is reversed by REV, providing novel biomarkers and indicating the therapeutic potential of REV in OSCC. Nature Publishing Group UK 2020-07-30 /pmc/articles/PMC8080807/ /pubmed/32728068 http://dx.doi.org/10.1038/s12276-020-0474-1 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kim, Jin Young Cho, Kyung Hwa Jeong, Bo Young Park, Chang Gyo Lee, Hoi Young Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title | Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title_full | Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title_fullStr | Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title_full_unstemmed | Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title_short | Zeb1 for RCP-induced oral cancer cell invasion and its suppression by resveratrol |
title_sort | zeb1 for rcp-induced oral cancer cell invasion and its suppression by resveratrol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080807/ https://www.ncbi.nlm.nih.gov/pubmed/32728068 http://dx.doi.org/10.1038/s12276-020-0474-1 |
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