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An inhibitory role of NEK6 in TGFβ/Smad signaling pathway

The NEK6 (NIMA-related kinases 6) is reported to play po-tential roles in tumorigenesis. Although it is suggested to function in several cellular pathways, the underlying mechanism in tumorigenesis is still largely unknown. In the present study, we discovered interaction of NEK6 with Smad4, a key me...

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Autores principales: Zuo, Jie, Ma, Haijie, Cai, Hao, Wu, Yanhua, Jiang, Wei, Yu, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576956/
https://www.ncbi.nlm.nih.gov/pubmed/25523445
http://dx.doi.org/10.5483/BMBRep.2015.48.8.225
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author Zuo, Jie
Ma, Haijie
Cai, Hao
Wu, Yanhua
Jiang, Wei
Yu, Long
author_facet Zuo, Jie
Ma, Haijie
Cai, Hao
Wu, Yanhua
Jiang, Wei
Yu, Long
author_sort Zuo, Jie
collection PubMed
description The NEK6 (NIMA-related kinases 6) is reported to play po-tential roles in tumorigenesis. Although it is suggested to function in several cellular pathways, the underlying mechanism in tumorigenesis is still largely unknown. In the present study, we discovered interaction of NEK6 with Smad4, a key member of transforming growth factor beta (TGFβ) pathway. Over-expression of NEK6 in hepatocellular carcinoma (HCC) cell lines suppresses TGFβ-mediated transcription activity in a kinase activity-dependent manner. In addition, NEK6 suppresses the cell growth arrest induced by TGFβ. Mechanically, NEK6 blocks nuclear translocation of Smad4, which is essential for TGFβ function. Moreover, we identified that NEK6 could be regulated by TGFβ and hypoxia. Our study sheds new light on the roles of NEK6 in canonical TGFβ/Smad pathway and tum-origenesis. [BMB Reports 2015; 48(8): 473-478]
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spelling pubmed-45769562015-09-30 An inhibitory role of NEK6 in TGFβ/Smad signaling pathway Zuo, Jie Ma, Haijie Cai, Hao Wu, Yanhua Jiang, Wei Yu, Long BMB Rep Research-Article The NEK6 (NIMA-related kinases 6) is reported to play po-tential roles in tumorigenesis. Although it is suggested to function in several cellular pathways, the underlying mechanism in tumorigenesis is still largely unknown. In the present study, we discovered interaction of NEK6 with Smad4, a key member of transforming growth factor beta (TGFβ) pathway. Over-expression of NEK6 in hepatocellular carcinoma (HCC) cell lines suppresses TGFβ-mediated transcription activity in a kinase activity-dependent manner. In addition, NEK6 suppresses the cell growth arrest induced by TGFβ. Mechanically, NEK6 blocks nuclear translocation of Smad4, which is essential for TGFβ function. Moreover, we identified that NEK6 could be regulated by TGFβ and hypoxia. Our study sheds new light on the roles of NEK6 in canonical TGFβ/Smad pathway and tum-origenesis. [BMB Reports 2015; 48(8): 473-478] Korean Society for Biochemistry and Molecular Biology 2015-08-31 /pmc/articles/PMC4576956/ /pubmed/25523445 http://dx.doi.org/10.5483/BMBRep.2015.48.8.225 Text en Copyright © 2015, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research-Article
Zuo, Jie
Ma, Haijie
Cai, Hao
Wu, Yanhua
Jiang, Wei
Yu, Long
An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title_full An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title_fullStr An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title_full_unstemmed An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title_short An inhibitory role of NEK6 in TGFβ/Smad signaling pathway
title_sort inhibitory role of nek6 in tgfβ/smad signaling pathway
topic Research-Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576956/
https://www.ncbi.nlm.nih.gov/pubmed/25523445
http://dx.doi.org/10.5483/BMBRep.2015.48.8.225
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