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NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC
Esophageal squamous cell carcinoma (ESCC) is a common subtype of esophageal cancer with high incidence. Surgery remains the main strategy for treatment of ESCC at early stage. However, the treatment outcome is unsatisfactory. Therefore, finding new therapeutics is of great importance. In the present...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827801/ https://www.ncbi.nlm.nih.gov/pubmed/35593463 http://dx.doi.org/10.3724/abbs.2022048 |
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author | Cheng, Wei Li, Guiyuan Ye, Zhou Hu, Jun Gao, Lixia Jia, Xiaoling Zhao, Suping Wang, Yan Zhou, Qin |
author_facet | Cheng, Wei Li, Guiyuan Ye, Zhou Hu, Jun Gao, Lixia Jia, Xiaoling Zhao, Suping Wang, Yan Zhou, Qin |
author_sort | Cheng, Wei |
collection | PubMed |
description | Esophageal squamous cell carcinoma (ESCC) is a common subtype of esophageal cancer with high incidence. Surgery remains the main strategy for treatment of ESCC at early stage. However, the treatment outcome is unsatisfactory. Therefore, finding new therapeutics is of great importance. In the present study, we measured the level of NEDD4L, an ubiquitin protein ligase, in clinical samples and investigated the effects of NEDD4L on cell viability, cell cycle progression, and glutamine metabolism in TE14 cells determined by CCK-8 assay, flow cytometry and biochemical analysis, respectively. The results show that NEDD4L is significantly decreased in ESCC specimens, and its decreased expression is associated with a poor clinical outcome. Overexpression of NEDD4L significantly inhibits cell viability, cell cycle progression, and glutamine metabolism in TE14 cells. Mechanistic study indicates that NEDD4L regulates tumor progression through ubiquitination of c-Myc and modulation of glutamine metabolism. NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in ESCC by ubiquitination of c-Myc to decrease the expressions of GLS1 and SLC1A5. Our findings highlight the importance of NEDD4L/c-Myc signaling in ESCC. |
format | Online Article Text |
id | pubmed-9827801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98278012023-02-10 NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC Cheng, Wei Li, Guiyuan Ye, Zhou Hu, Jun Gao, Lixia Jia, Xiaoling Zhao, Suping Wang, Yan Zhou, Qin Acta Biochim Biophys Sin (Shanghai) Research Article Esophageal squamous cell carcinoma (ESCC) is a common subtype of esophageal cancer with high incidence. Surgery remains the main strategy for treatment of ESCC at early stage. However, the treatment outcome is unsatisfactory. Therefore, finding new therapeutics is of great importance. In the present study, we measured the level of NEDD4L, an ubiquitin protein ligase, in clinical samples and investigated the effects of NEDD4L on cell viability, cell cycle progression, and glutamine metabolism in TE14 cells determined by CCK-8 assay, flow cytometry and biochemical analysis, respectively. The results show that NEDD4L is significantly decreased in ESCC specimens, and its decreased expression is associated with a poor clinical outcome. Overexpression of NEDD4L significantly inhibits cell viability, cell cycle progression, and glutamine metabolism in TE14 cells. Mechanistic study indicates that NEDD4L regulates tumor progression through ubiquitination of c-Myc and modulation of glutamine metabolism. NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in ESCC by ubiquitination of c-Myc to decrease the expressions of GLS1 and SLC1A5. Our findings highlight the importance of NEDD4L/c-Myc signaling in ESCC. Oxford University Press 2022-05-16 /pmc/articles/PMC9827801/ /pubmed/35593463 http://dx.doi.org/10.3724/abbs.2022048 Text en © The Author(s) 2021. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Research Article Cheng, Wei Li, Guiyuan Ye, Zhou Hu, Jun Gao, Lixia Jia, Xiaoling Zhao, Suping Wang, Yan Zhou, Qin NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title | NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title_full | NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title_fullStr | NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title_full_unstemmed | NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title_short | NEDD4L inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-Myc: NEDD4L and c-Myc coordinate to regulate ESCC |
title_sort | nedd4l inhibits cell viability, cell cycle progression, and glutamine metabolism in esophageal squamous cell carcinoma via ubiquitination of c-myc: nedd4l and c-myc coordinate to regulate escc |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827801/ https://www.ncbi.nlm.nih.gov/pubmed/35593463 http://dx.doi.org/10.3724/abbs.2022048 |
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