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NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development

The present study aimed to discuss the effects and relative mechanisms of NEDD4 E3 ubiquitin protein ligase (NEDD4) in cutaneous melanoma (CMM) occurrence and development. Clinical cancer and adjacent normal tissues samples were collected to analyze pathological changes and protein expression of NED...

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Detalles Bibliográficos
Autores principales: Cheng, Fang, Cheng, Yi, Zhao, Xiaoling, An, Lihui, Yang, Linfang, Li, Zihan, Zhang, Lei, He, Runzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506948/
https://www.ncbi.nlm.nih.gov/pubmed/34650630
http://dx.doi.org/10.3892/etm.2021.10818
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author Cheng, Fang
Cheng, Yi
Zhao, Xiaoling
An, Lihui
Yang, Linfang
Li, Zihan
Zhang, Lei
He, Runzhi
author_facet Cheng, Fang
Cheng, Yi
Zhao, Xiaoling
An, Lihui
Yang, Linfang
Li, Zihan
Zhang, Lei
He, Runzhi
author_sort Cheng, Fang
collection PubMed
description The present study aimed to discuss the effects and relative mechanisms of NEDD4 E3 ubiquitin protein ligase (NEDD4) in cutaneous melanoma (CMM) occurrence and development. Clinical cancer and adjacent normal tissues samples were collected to analyze pathological changes and protein expression of NEDD4. Moreover, small interfering (si)RNA was used to knockdown NEDD4 expression in SK-MEL-2 and Malme-3M cells. Cellular proliferation, apoptosis, invasiveness and migration were examined using colony formation, flow cytometric, Transwell and wound-healing assays, respectively. In addition, the relative mRNA and protein expression levels of NEDD4, notch receptor 1 (Notch1) and PTEN were evaluated via reverse transcription-quantitative (RT-q) PCR and western blotting. It was found that NEDD4 mRNA and protein expression were significantly upregulated (both P<0.01). Following NEDD4-knockdown, colony number was significantly decreased, while the apoptotic rate was significantly increased, the invasive cell number was significantly inhibited and the wound-healing capacity was significantly decreased. Following si-NEDD4 transfection, RT-qPCR and western blotting revealed that NEDD4 and Notch1 mRNA and protein expression levels were significantly downregulated, while those of PTEN were significantly upregulated in the SK-MEL-2 and Malme-3M cell lines. Collectively, the current results suggest that NEDD4-knockdown effectively suppressed CMM biological activity by regulating the Notch1/PTEN pathway in vitro.
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spelling pubmed-85069482021-10-13 NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development Cheng, Fang Cheng, Yi Zhao, Xiaoling An, Lihui Yang, Linfang Li, Zihan Zhang, Lei He, Runzhi Exp Ther Med Articles The present study aimed to discuss the effects and relative mechanisms of NEDD4 E3 ubiquitin protein ligase (NEDD4) in cutaneous melanoma (CMM) occurrence and development. Clinical cancer and adjacent normal tissues samples were collected to analyze pathological changes and protein expression of NEDD4. Moreover, small interfering (si)RNA was used to knockdown NEDD4 expression in SK-MEL-2 and Malme-3M cells. Cellular proliferation, apoptosis, invasiveness and migration were examined using colony formation, flow cytometric, Transwell and wound-healing assays, respectively. In addition, the relative mRNA and protein expression levels of NEDD4, notch receptor 1 (Notch1) and PTEN were evaluated via reverse transcription-quantitative (RT-q) PCR and western blotting. It was found that NEDD4 mRNA and protein expression were significantly upregulated (both P<0.01). Following NEDD4-knockdown, colony number was significantly decreased, while the apoptotic rate was significantly increased, the invasive cell number was significantly inhibited and the wound-healing capacity was significantly decreased. Following si-NEDD4 transfection, RT-qPCR and western blotting revealed that NEDD4 and Notch1 mRNA and protein expression levels were significantly downregulated, while those of PTEN were significantly upregulated in the SK-MEL-2 and Malme-3M cell lines. Collectively, the current results suggest that NEDD4-knockdown effectively suppressed CMM biological activity by regulating the Notch1/PTEN pathway in vitro. D.A. Spandidos 2021-12 2021-09-28 /pmc/articles/PMC8506948/ /pubmed/34650630 http://dx.doi.org/10.3892/etm.2021.10818 Text en Copyright: © Cheng et al. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Cheng, Fang
Cheng, Yi
Zhao, Xiaoling
An, Lihui
Yang, Linfang
Li, Zihan
Zhang, Lei
He, Runzhi
NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title_full NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title_fullStr NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title_full_unstemmed NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title_short NEDD4 E3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
title_sort nedd4 e3 ubiquitin protein ligase serves an important role in cutaneous melanoma occurrence and development
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506948/
https://www.ncbi.nlm.nih.gov/pubmed/34650630
http://dx.doi.org/10.3892/etm.2021.10818
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