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Mitosis-related gene CENP-U as a potential biomarker in malignancy
BACKGROUND: Centromere protein U (CENP-U) is a component of the kinetochore and can regulate the cell cycle as a receptor of polo-like kinase 1 (PLK1). Recent studies have partially identified the role of CENP-U in tumor progression, but the underlying mechanisms of CENP-U in tumor immunity remain o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743736/ https://www.ncbi.nlm.nih.gov/pubmed/35071438 http://dx.doi.org/10.21037/atm-21-6516 |
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author | Shao, Changjian Wang, Yuanyong Duan, Hongtao Ding, Peng Zhang, Yimeng Ning, Jiayi Han, Jing Jiang, Tao Yan, Xiaolong |
author_facet | Shao, Changjian Wang, Yuanyong Duan, Hongtao Ding, Peng Zhang, Yimeng Ning, Jiayi Han, Jing Jiang, Tao Yan, Xiaolong |
author_sort | Shao, Changjian |
collection | PubMed |
description | BACKGROUND: Centromere protein U (CENP-U) is a component of the kinetochore and can regulate the cell cycle as a receptor of polo-like kinase 1 (PLK1). Recent studies have partially identified the role of CENP-U in tumor progression, but the underlying mechanisms of CENP-U in tumor immunity remain obscure. METHODS: We performed pan-cancer analysis to evaluate the role of CENP-U in immunity and proliferation with data from The Cancer Genome Atlas (TCGA), Cancer Cell Line Encyclopedia (CCLE) datasets, and Genotype-Tissue Expression (GTEx) project. Results of CENP-U expression and related clinicopathological data were obtained to show the expression levels, prognosis, tumor progression, immune neoantigens, and immune checkpoints of CENP-U in 33 tumors. The Tumor Immune Estimation Resource (TIMER) dataset was used to analyze immune infiltration scores. RESULTS: Results of the pan-cancer analysis demonstrated that CENP-U is differentially expressed in normal tissues and common tumor tissues. Moreover, differentially expressed CENP-U was also identified between matched normal and tumor tissues, and the high expression level of CENP-U was associated with poor prognosis for 33 kinds of tumor except for that of thymoma (THYM) and lymphoid neoplasm diffuse large B-cell lymphoma (DLBC). Furthermore, the correlation between CENP-U expression and immune checkpoints and immune neoantigens was determined. In addition, CENP-U expression was correlated with tumor-infiltrating immune cells especially in THYM but not in lung squamous cell carcinoma (LUSC), esophageal carcinoma (ESCA), or lung adenocarcinoma (LUAD). Finally, gene set enrichment analysis (GSEA) indicated that CENP-U is critically involved in tumor proliferation, immunity, and metabolism. CONCLUSIONS: CENP-U, a mitosis-related kinase, was found to be differentially expressed across different cancer types and to play an important role in tumor progression and immunity. CENP-U holds the potential to be a prognostic marker, whose targeting may provide therapeutic benefit. |
format | Online Article Text |
id | pubmed-8743736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87437362022-01-21 Mitosis-related gene CENP-U as a potential biomarker in malignancy Shao, Changjian Wang, Yuanyong Duan, Hongtao Ding, Peng Zhang, Yimeng Ning, Jiayi Han, Jing Jiang, Tao Yan, Xiaolong Ann Transl Med Original Article BACKGROUND: Centromere protein U (CENP-U) is a component of the kinetochore and can regulate the cell cycle as a receptor of polo-like kinase 1 (PLK1). Recent studies have partially identified the role of CENP-U in tumor progression, but the underlying mechanisms of CENP-U in tumor immunity remain obscure. METHODS: We performed pan-cancer analysis to evaluate the role of CENP-U in immunity and proliferation with data from The Cancer Genome Atlas (TCGA), Cancer Cell Line Encyclopedia (CCLE) datasets, and Genotype-Tissue Expression (GTEx) project. Results of CENP-U expression and related clinicopathological data were obtained to show the expression levels, prognosis, tumor progression, immune neoantigens, and immune checkpoints of CENP-U in 33 tumors. The Tumor Immune Estimation Resource (TIMER) dataset was used to analyze immune infiltration scores. RESULTS: Results of the pan-cancer analysis demonstrated that CENP-U is differentially expressed in normal tissues and common tumor tissues. Moreover, differentially expressed CENP-U was also identified between matched normal and tumor tissues, and the high expression level of CENP-U was associated with poor prognosis for 33 kinds of tumor except for that of thymoma (THYM) and lymphoid neoplasm diffuse large B-cell lymphoma (DLBC). Furthermore, the correlation between CENP-U expression and immune checkpoints and immune neoantigens was determined. In addition, CENP-U expression was correlated with tumor-infiltrating immune cells especially in THYM but not in lung squamous cell carcinoma (LUSC), esophageal carcinoma (ESCA), or lung adenocarcinoma (LUAD). Finally, gene set enrichment analysis (GSEA) indicated that CENP-U is critically involved in tumor proliferation, immunity, and metabolism. CONCLUSIONS: CENP-U, a mitosis-related kinase, was found to be differentially expressed across different cancer types and to play an important role in tumor progression and immunity. CENP-U holds the potential to be a prognostic marker, whose targeting may provide therapeutic benefit. AME Publishing Company 2021-12 /pmc/articles/PMC8743736/ /pubmed/35071438 http://dx.doi.org/10.21037/atm-21-6516 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Shao, Changjian Wang, Yuanyong Duan, Hongtao Ding, Peng Zhang, Yimeng Ning, Jiayi Han, Jing Jiang, Tao Yan, Xiaolong Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title | Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title_full | Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title_fullStr | Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title_full_unstemmed | Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title_short | Mitosis-related gene CENP-U as a potential biomarker in malignancy |
title_sort | mitosis-related gene cenp-u as a potential biomarker in malignancy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8743736/ https://www.ncbi.nlm.nih.gov/pubmed/35071438 http://dx.doi.org/10.21037/atm-21-6516 |
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