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E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability
E3 ubiquitin ligase RNF126 (ring finger protein 126) is highly expressed in various cancers and strongly associated with tumorigenesis. However, its specific function in bladder cancer (BCa) is still debatable. Here, we found that RNF126 was significantly upregulated in BCa tissue by TCGA database,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933351/ https://www.ncbi.nlm.nih.gov/pubmed/33664240 http://dx.doi.org/10.1038/s41419-021-03521-1 |
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author | Xu, Huimin Ju, Lingao Xiong, Yaoyi Yu, Mengxue Zhou, Fenfang Qian, Kaiyu Wang, Gang Xiao, Yu Wang, Xinghuan |
author_facet | Xu, Huimin Ju, Lingao Xiong, Yaoyi Yu, Mengxue Zhou, Fenfang Qian, Kaiyu Wang, Gang Xiao, Yu Wang, Xinghuan |
author_sort | Xu, Huimin |
collection | PubMed |
description | E3 ubiquitin ligase RNF126 (ring finger protein 126) is highly expressed in various cancers and strongly associated with tumorigenesis. However, its specific function in bladder cancer (BCa) is still debatable. Here, we found that RNF126 was significantly upregulated in BCa tissue by TCGA database, and our studies indicated that downregulation of RNF126 significantly inhibited cell proliferation and metastasis through the EGFR/PI3K/AKT signaling pathway in BCa cells. Furthermore, we identified PTEN, an inhibitor of the PI3K/AKT signaling pathway, as a novel substrate for RNF126. By co-immunoprecipitation assays, we proved that RNF126 directly interacts with PTEN. Predominantly, PTEN binds to the C-terminal containing the RING domain of RNF126. The in vivo ubiquitination assay showed that RNF126 specifically regulates PTEN stability through poly-ubiquitination. Furthermore, PTEN knockdown restored cell proliferation, metastasis, and tumor formation of BCa cells inhibited by RNF126 silencing in vitro and in vivo. In conclusion, these results identified RNF126 as an oncogene that functions through ubiquitination and degradation of PTEN in BCa. |
format | Online Article Text |
id | pubmed-7933351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79333512021-03-19 E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability Xu, Huimin Ju, Lingao Xiong, Yaoyi Yu, Mengxue Zhou, Fenfang Qian, Kaiyu Wang, Gang Xiao, Yu Wang, Xinghuan Cell Death Dis Article E3 ubiquitin ligase RNF126 (ring finger protein 126) is highly expressed in various cancers and strongly associated with tumorigenesis. However, its specific function in bladder cancer (BCa) is still debatable. Here, we found that RNF126 was significantly upregulated in BCa tissue by TCGA database, and our studies indicated that downregulation of RNF126 significantly inhibited cell proliferation and metastasis through the EGFR/PI3K/AKT signaling pathway in BCa cells. Furthermore, we identified PTEN, an inhibitor of the PI3K/AKT signaling pathway, as a novel substrate for RNF126. By co-immunoprecipitation assays, we proved that RNF126 directly interacts with PTEN. Predominantly, PTEN binds to the C-terminal containing the RING domain of RNF126. The in vivo ubiquitination assay showed that RNF126 specifically regulates PTEN stability through poly-ubiquitination. Furthermore, PTEN knockdown restored cell proliferation, metastasis, and tumor formation of BCa cells inhibited by RNF126 silencing in vitro and in vivo. In conclusion, these results identified RNF126 as an oncogene that functions through ubiquitination and degradation of PTEN in BCa. Nature Publishing Group UK 2021-03-04 /pmc/articles/PMC7933351/ /pubmed/33664240 http://dx.doi.org/10.1038/s41419-021-03521-1 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Xu, Huimin Ju, Lingao Xiong, Yaoyi Yu, Mengxue Zhou, Fenfang Qian, Kaiyu Wang, Gang Xiao, Yu Wang, Xinghuan E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title | E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title_full | E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title_fullStr | E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title_full_unstemmed | E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title_short | E3 ubiquitin ligase RNF126 affects bladder cancer progression through regulation of PTEN stability |
title_sort | e3 ubiquitin ligase rnf126 affects bladder cancer progression through regulation of pten stability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933351/ https://www.ncbi.nlm.nih.gov/pubmed/33664240 http://dx.doi.org/10.1038/s41419-021-03521-1 |
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