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Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma

Cumulative evidence indicates that the abnormal regulation of the NEDD4 family of E3-ubiquitin ligases participates in the tumorigenesis and development of cancer. However, their role in lung adenocarcinoma (LUAD) remains unclear. This study comprehensively analyzed the NEDD4 family in LUAD data set...

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Autores principales: Li, Guoyin, Song, Zewen, Wu, Changjing, Li, XiaoYan, Zhao, Liping, Tong, Binghua, Guo, Zhenni, Sun, Meiqing, Zhao, Jin, Zhang, Huina, Jia, Lintao, Li, Shengqing, Wang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800232/
https://www.ncbi.nlm.nih.gov/pubmed/35090513
http://dx.doi.org/10.1186/s12967-022-03247-4
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author Li, Guoyin
Song, Zewen
Wu, Changjing
Li, XiaoYan
Zhao, Liping
Tong, Binghua
Guo, Zhenni
Sun, Meiqing
Zhao, Jin
Zhang, Huina
Jia, Lintao
Li, Shengqing
Wang, Lei
author_facet Li, Guoyin
Song, Zewen
Wu, Changjing
Li, XiaoYan
Zhao, Liping
Tong, Binghua
Guo, Zhenni
Sun, Meiqing
Zhao, Jin
Zhang, Huina
Jia, Lintao
Li, Shengqing
Wang, Lei
author_sort Li, Guoyin
collection PubMed
description Cumulative evidence indicates that the abnormal regulation of the NEDD4 family of E3-ubiquitin ligases participates in the tumorigenesis and development of cancer. However, their role in lung adenocarcinoma (LUAD) remains unclear. This study comprehensively analyzed the NEDD4 family in LUAD data sets from public databases and found only NEDD4L was associated with the overall survival of LUAD patients. Gene set enrichment analysis (GSEA) indicated that NEDD4L might be involved in the regulation of mTORC1 pathway. Both cytological and clinical assays showed that NEDD4L inhibited the activity of the mTOR signaling pathway. In vivo and in vitro experiments showed that NEDD4L could significantly inhibit the proliferation of LUAD cells. In addition, this study also found that the expression of NEDD4L was regulated by EGFR signaling. These findings firstly revealed that NEDD4L mediates an interplay between EGFR and mTOR pathways in LUAD, and suggest that NEDD4L held great potential as a novel biomarker and therapeutic target for LUAD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03247-4.
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spelling pubmed-88002322022-02-02 Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma Li, Guoyin Song, Zewen Wu, Changjing Li, XiaoYan Zhao, Liping Tong, Binghua Guo, Zhenni Sun, Meiqing Zhao, Jin Zhang, Huina Jia, Lintao Li, Shengqing Wang, Lei J Transl Med Research Cumulative evidence indicates that the abnormal regulation of the NEDD4 family of E3-ubiquitin ligases participates in the tumorigenesis and development of cancer. However, their role in lung adenocarcinoma (LUAD) remains unclear. This study comprehensively analyzed the NEDD4 family in LUAD data sets from public databases and found only NEDD4L was associated with the overall survival of LUAD patients. Gene set enrichment analysis (GSEA) indicated that NEDD4L might be involved in the regulation of mTORC1 pathway. Both cytological and clinical assays showed that NEDD4L inhibited the activity of the mTOR signaling pathway. In vivo and in vitro experiments showed that NEDD4L could significantly inhibit the proliferation of LUAD cells. In addition, this study also found that the expression of NEDD4L was regulated by EGFR signaling. These findings firstly revealed that NEDD4L mediates an interplay between EGFR and mTOR pathways in LUAD, and suggest that NEDD4L held great potential as a novel biomarker and therapeutic target for LUAD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-022-03247-4. BioMed Central 2022-01-28 /pmc/articles/PMC8800232/ /pubmed/35090513 http://dx.doi.org/10.1186/s12967-022-03247-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Guoyin
Song, Zewen
Wu, Changjing
Li, XiaoYan
Zhao, Liping
Tong, Binghua
Guo, Zhenni
Sun, Meiqing
Zhao, Jin
Zhang, Huina
Jia, Lintao
Li, Shengqing
Wang, Lei
Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title_full Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title_fullStr Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title_full_unstemmed Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title_short Downregulation of NEDD4L by EGFR signaling promotes the development of lung adenocarcinoma
title_sort downregulation of nedd4l by egfr signaling promotes the development of lung adenocarcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800232/
https://www.ncbi.nlm.nih.gov/pubmed/35090513
http://dx.doi.org/10.1186/s12967-022-03247-4
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