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Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma

Objectives: Never in mitosis gene A-related kinase 2 (NEK2) has been implicated in tumorigenesis in various tissues, but its function in clear cell renal cell carcinoma (ccRCC) tumorigenesis is unclear. We evaluated the correlation between NEK2 expression and ccRCC. Methods: Immunohistochemistry ana...

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Autores principales: Wang, Chenfeng, Huang, Yan, Ma, Xin, Wang, Baojun, Zhang, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689635/
https://www.ncbi.nlm.nih.gov/pubmed/34910592
http://dx.doi.org/10.1177/20587384211065893
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author Wang, Chenfeng
Huang, Yan
Ma, Xin
Wang, Baojun
Zhang, Xu
author_facet Wang, Chenfeng
Huang, Yan
Ma, Xin
Wang, Baojun
Zhang, Xu
author_sort Wang, Chenfeng
collection PubMed
description Objectives: Never in mitosis gene A-related kinase 2 (NEK2) has been implicated in tumorigenesis in various tissues, but its function in clear cell renal cell carcinoma (ccRCC) tumorigenesis is unclear. We evaluated the correlation between NEK2 expression and ccRCC. Methods: Immunohistochemistry analysis of NEK2 protein was done on high-density multi-organ Human Cancer tissue microarray derived from the patient samples from clear cell renal cell carcinoma. We used multiple clinical cohorts to analyze the NEK2 immunohistochemical staining expression across human cancers. The cancer genome atlas (TCGA) data analysis of NEK2 was done through UALCAN web servers. Association of NEK2 and Kaplan–Meier survival analysis was done on both of our clinical database and available TCGA datasets. Results: Using the UALCAN cancer transcriptional data analysis website, we found that NEK2 is overexpressed in ccRCC, and its expression was associated with overall survival. According to the analyses of our own clinical database and immunohistochemical staining, protein levels of NEK2 were elevated in renal carcinoma compared to adjacent normal tissues. Kaplan–Meier survival analysis of both UALCAN and our database showed that high expression of NEK2 was associated with a poor prognosis. Multivariate and univariate analyses showed that NEK2 expression was closely related to a poor prognosis. The findings suggest that NEK2 is associated with ccRCC. Conclusion: These studies show that NEK2 is over-expressed in clear cell renal cell carcinoma and plays an essential role in cancer cell survival, as such NEK2 could serve as a novel potential target for therapeutic intervention in ccRCC.
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spelling pubmed-86896352021-12-22 Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma Wang, Chenfeng Huang, Yan Ma, Xin Wang, Baojun Zhang, Xu Int J Immunopathol Pharmacol Original Research Article Objectives: Never in mitosis gene A-related kinase 2 (NEK2) has been implicated in tumorigenesis in various tissues, but its function in clear cell renal cell carcinoma (ccRCC) tumorigenesis is unclear. We evaluated the correlation between NEK2 expression and ccRCC. Methods: Immunohistochemistry analysis of NEK2 protein was done on high-density multi-organ Human Cancer tissue microarray derived from the patient samples from clear cell renal cell carcinoma. We used multiple clinical cohorts to analyze the NEK2 immunohistochemical staining expression across human cancers. The cancer genome atlas (TCGA) data analysis of NEK2 was done through UALCAN web servers. Association of NEK2 and Kaplan–Meier survival analysis was done on both of our clinical database and available TCGA datasets. Results: Using the UALCAN cancer transcriptional data analysis website, we found that NEK2 is overexpressed in ccRCC, and its expression was associated with overall survival. According to the analyses of our own clinical database and immunohistochemical staining, protein levels of NEK2 were elevated in renal carcinoma compared to adjacent normal tissues. Kaplan–Meier survival analysis of both UALCAN and our database showed that high expression of NEK2 was associated with a poor prognosis. Multivariate and univariate analyses showed that NEK2 expression was closely related to a poor prognosis. The findings suggest that NEK2 is associated with ccRCC. Conclusion: These studies show that NEK2 is over-expressed in clear cell renal cell carcinoma and plays an essential role in cancer cell survival, as such NEK2 could serve as a novel potential target for therapeutic intervention in ccRCC. SAGE Publications 2021-12-15 /pmc/articles/PMC8689635/ /pubmed/34910592 http://dx.doi.org/10.1177/20587384211065893 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Wang, Chenfeng
Huang, Yan
Ma, Xin
Wang, Baojun
Zhang, Xu
Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title_full Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title_fullStr Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title_full_unstemmed Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title_short Overexpression of NEK2 is correlated with poor prognosis in human clear cell renal cell carcinoma
title_sort overexpression of nek2 is correlated with poor prognosis in human clear cell renal cell carcinoma
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689635/
https://www.ncbi.nlm.nih.gov/pubmed/34910592
http://dx.doi.org/10.1177/20587384211065893
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