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USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1

BACKGROUND: USP51 is a deubiquitinase (DUB), that is involved in diverse cellular processes. Accumulating evidence has demonstrated that USP51 contributes to cancer development. However, its impact on non-small cell lung carcinoma (NSCLC) cell malignancy is largely unknown. METHODS: In this study, w...

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Autores principales: Chen, Jin, Wu, Zhongqiu, Deng, Wenyi, Tang, Minying, Wu, Lvying, Lin, Na, Chen, Liuyan, Fu, Yunfeng, Zhao, Min, Chen, Changguo, Li, Wenting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329790/
https://www.ncbi.nlm.nih.gov/pubmed/37422632
http://dx.doi.org/10.1186/s12967-023-04304-2
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author Chen, Jin
Wu, Zhongqiu
Deng, Wenyi
Tang, Minying
Wu, Lvying
Lin, Na
Chen, Liuyan
Fu, Yunfeng
Zhao, Min
Chen, Changguo
Li, Wenting
author_facet Chen, Jin
Wu, Zhongqiu
Deng, Wenyi
Tang, Minying
Wu, Lvying
Lin, Na
Chen, Liuyan
Fu, Yunfeng
Zhao, Min
Chen, Changguo
Li, Wenting
author_sort Chen, Jin
collection PubMed
description BACKGROUND: USP51 is a deubiquitinase (DUB), that is involved in diverse cellular processes. Accumulating evidence has demonstrated that USP51 contributes to cancer development. However, its impact on non-small cell lung carcinoma (NSCLC) cell malignancy is largely unknown. METHODS: In this study, we performed bioinformatics analysis on a dataset from The Cancer Genome Atlas to determine the association between USP51 and cell stemness marker expression in NSCLC patients. RT‒qPCR, Western blotting, and flow cytometry were performed to examine the effects of USP51 depletion on stemness marker expression. Colony formation and tumor sphere formation assays were used to assess the stemness of NSCLC cells. A cycloheximide chase time-course assay and a polyubiquitination assay were carried out to analyze the effects of USP51 on the TWIST1 protein level. TWIST1 was overexpressed in USP51 knockdown NSCLC cells to determine whether TWIST1 is required. The effect of USP51 on the in vivo growth of NSCLC cells was tested through subcutaneous injections in mice. RESULTS: We found that USP51 deubiquitinates TWIST1, which is significantly upregulated in the tissues of patients with NSCLC and is closely associated with poor prognosis. USP51 expression was positively correlated with the expression of stemness marker CD44, SOX2, NANOG, and OCT4 in NSCLC patients. USP51 depletion attenuated mRNA, protein, and cell surface expression of stemness markers and the stemness of NSCLC cells. Ectopic USP51 expression potentiated the stability of the TWIST1 protein by attenuating its polyubiquitination. In addition, TWIST1 re-expression in NSCLC cells reversed the inhibitory effect of USP51 knockdown on cell stemness. Furthermore, the in vivo results confirmed the suppressive effect of USP51 depletion on NSCLC cell growth. CONCLUSIONS: Our results show that USP51 maintains the stemness of NSCLC cells by deubiquitinating TWIST1. Knocking it down reduces both cell stemness and growth of NSCLC cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04304-2.
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spelling pubmed-103297902023-07-10 USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1 Chen, Jin Wu, Zhongqiu Deng, Wenyi Tang, Minying Wu, Lvying Lin, Na Chen, Liuyan Fu, Yunfeng Zhao, Min Chen, Changguo Li, Wenting J Transl Med Research BACKGROUND: USP51 is a deubiquitinase (DUB), that is involved in diverse cellular processes. Accumulating evidence has demonstrated that USP51 contributes to cancer development. However, its impact on non-small cell lung carcinoma (NSCLC) cell malignancy is largely unknown. METHODS: In this study, we performed bioinformatics analysis on a dataset from The Cancer Genome Atlas to determine the association between USP51 and cell stemness marker expression in NSCLC patients. RT‒qPCR, Western blotting, and flow cytometry were performed to examine the effects of USP51 depletion on stemness marker expression. Colony formation and tumor sphere formation assays were used to assess the stemness of NSCLC cells. A cycloheximide chase time-course assay and a polyubiquitination assay were carried out to analyze the effects of USP51 on the TWIST1 protein level. TWIST1 was overexpressed in USP51 knockdown NSCLC cells to determine whether TWIST1 is required. The effect of USP51 on the in vivo growth of NSCLC cells was tested through subcutaneous injections in mice. RESULTS: We found that USP51 deubiquitinates TWIST1, which is significantly upregulated in the tissues of patients with NSCLC and is closely associated with poor prognosis. USP51 expression was positively correlated with the expression of stemness marker CD44, SOX2, NANOG, and OCT4 in NSCLC patients. USP51 depletion attenuated mRNA, protein, and cell surface expression of stemness markers and the stemness of NSCLC cells. Ectopic USP51 expression potentiated the stability of the TWIST1 protein by attenuating its polyubiquitination. In addition, TWIST1 re-expression in NSCLC cells reversed the inhibitory effect of USP51 knockdown on cell stemness. Furthermore, the in vivo results confirmed the suppressive effect of USP51 depletion on NSCLC cell growth. CONCLUSIONS: Our results show that USP51 maintains the stemness of NSCLC cells by deubiquitinating TWIST1. Knocking it down reduces both cell stemness and growth of NSCLC cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04304-2. BioMed Central 2023-07-08 /pmc/articles/PMC10329790/ /pubmed/37422632 http://dx.doi.org/10.1186/s12967-023-04304-2 Text en © The Author(s) 2023 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 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
Chen, Jin
Wu, Zhongqiu
Deng, Wenyi
Tang, Minying
Wu, Lvying
Lin, Na
Chen, Liuyan
Fu, Yunfeng
Zhao, Min
Chen, Changguo
Li, Wenting
USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title_full USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title_fullStr USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title_full_unstemmed USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title_short USP51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating TWIST1
title_sort usp51 promotes non-small cell lung carcinoma cell stemness by deubiquitinating twist1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329790/
https://www.ncbi.nlm.nih.gov/pubmed/37422632
http://dx.doi.org/10.1186/s12967-023-04304-2
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