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The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization
Deubiquitinating enzyme OTU domain‐containing ubiquitin aldehyde‐binding proteins 1 (OTUB1) has been shown to have an essential role in multiple carcinomas. However, the function of OTUB1 in papillary thyroid cancer (PTC) and the underlying mechanisms regulating PTC cells proliferation remain poorly...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642681/ https://www.ncbi.nlm.nih.gov/pubmed/34773364 http://dx.doi.org/10.1111/jcmm.17020 |
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author | Xie, Peiyi Chao, Qing Mao, Jiuang Liu, Yue Fang, Jiayu Xie, Jing Zhen, Jing Ding, Yongqi Fu, Bidong Ke, Yun Huang, Da |
author_facet | Xie, Peiyi Chao, Qing Mao, Jiuang Liu, Yue Fang, Jiayu Xie, Jing Zhen, Jing Ding, Yongqi Fu, Bidong Ke, Yun Huang, Da |
author_sort | Xie, Peiyi |
collection | PubMed |
description | Deubiquitinating enzyme OTU domain‐containing ubiquitin aldehyde‐binding proteins 1 (OTUB1) has been shown to have an essential role in multiple carcinomas. However, the function of OTUB1 in papillary thyroid cancer (PTC) and the underlying mechanisms regulating PTC cells proliferation remain poorly understood. In this study, OTUB1 was significantly upregulated in papillary thyroid carcinoma tissues and cells. Through in vitro and in vivo experiments, knockdown of OTUB1 suppressed PTC cells growth whereas OTUB1 overexpression enhanced the proliferation ability of PTC cells. Moreover, the eyes absent homologue 1 (EYA1) was recognized as a potential target of OTUB1 through mass spectrometry analysis, and we further verified that EYA1 protein level was positively correlated with OTUB1 expression in PTC cells and clinical samples. Mechanistically, OTUB1 could interact with EYA1 directly and deubiquitinate EYA1 to stabilize it. At last, EYA1 was found to play an essential role in OTUB1‐derived PTC cells growth. Overall, our investigation reveals that OTUB1 is a previously unrecognized oncogenic factor in PTC cells proliferation and suggests that OTUB1 might be a novel therapeutic target in PTC. |
format | Online Article Text |
id | pubmed-8642681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86426812021-12-15 The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization Xie, Peiyi Chao, Qing Mao, Jiuang Liu, Yue Fang, Jiayu Xie, Jing Zhen, Jing Ding, Yongqi Fu, Bidong Ke, Yun Huang, Da J Cell Mol Med Original Articles Deubiquitinating enzyme OTU domain‐containing ubiquitin aldehyde‐binding proteins 1 (OTUB1) has been shown to have an essential role in multiple carcinomas. However, the function of OTUB1 in papillary thyroid cancer (PTC) and the underlying mechanisms regulating PTC cells proliferation remain poorly understood. In this study, OTUB1 was significantly upregulated in papillary thyroid carcinoma tissues and cells. Through in vitro and in vivo experiments, knockdown of OTUB1 suppressed PTC cells growth whereas OTUB1 overexpression enhanced the proliferation ability of PTC cells. Moreover, the eyes absent homologue 1 (EYA1) was recognized as a potential target of OTUB1 through mass spectrometry analysis, and we further verified that EYA1 protein level was positively correlated with OTUB1 expression in PTC cells and clinical samples. Mechanistically, OTUB1 could interact with EYA1 directly and deubiquitinate EYA1 to stabilize it. At last, EYA1 was found to play an essential role in OTUB1‐derived PTC cells growth. Overall, our investigation reveals that OTUB1 is a previously unrecognized oncogenic factor in PTC cells proliferation and suggests that OTUB1 might be a novel therapeutic target in PTC. John Wiley and Sons Inc. 2021-11-12 2021-12 /pmc/articles/PMC8642681/ /pubmed/34773364 http://dx.doi.org/10.1111/jcmm.17020 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Xie, Peiyi Chao, Qing Mao, Jiuang Liu, Yue Fang, Jiayu Xie, Jing Zhen, Jing Ding, Yongqi Fu, Bidong Ke, Yun Huang, Da The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title | The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title_full | The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title_fullStr | The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title_full_unstemmed | The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title_short | The deubiquitinase OTUB1 fosters papillary thyroid carcinoma growth through EYA1 stabilization |
title_sort | deubiquitinase otub1 fosters papillary thyroid carcinoma growth through eya1 stabilization |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642681/ https://www.ncbi.nlm.nih.gov/pubmed/34773364 http://dx.doi.org/10.1111/jcmm.17020 |
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