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Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer
The tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation proteins (14-3-3) participate in the tumorigenesis and progression of numerous malignances, but their precise prognostic values in breast cancer (BrCa) remain unknown. Here, we investigated the expression profiles and prognostic role...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732302/ https://www.ncbi.nlm.nih.gov/pubmed/33052135 http://dx.doi.org/10.18632/aging.103919 |
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author | Mei, Jie Liu, Yan Xu, Rui Hao, Leiyu Qin, An Chu, Chunqiang Zhu, Yichao Liu, Xiao |
author_facet | Mei, Jie Liu, Yan Xu, Rui Hao, Leiyu Qin, An Chu, Chunqiang Zhu, Yichao Liu, Xiao |
author_sort | Mei, Jie |
collection | PubMed |
description | The tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation proteins (14-3-3) participate in the tumorigenesis and progression of numerous malignances, but their precise prognostic values in breast cancer (BrCa) remain unknown. Here, we investigated the expression profiles and prognostic roles of 14-3-3 isoforms by employing multiple online databases. The transcriptional levels of most 14-3-3 isoforms in BrCa tissues were significantly higher than those in normal tissues. High mRNA expression of 14-3-3 beta/sigma/theta/zeta was significantly associated with poor overall survival (OS) in BrCa patients, while high mRNA expression of 14-3-3 epsilon was notably related to favorable OS. High mRNA expression of 14-3-3 beta/gamma/sigma/theta/zeta was significantly associated with poor relapse-free survival (RFS) in BrCa patients. A high mutation rate of 14-3-3 was determined to be associated with poor clinical outcomes. In addition, 14-3-3 expression was correlated with the infiltration of specific immune cells types. Analysis of the breast-specific protein-protein interaction (PPI) network suggested that 14-3-3 proteins were involved in several potential oncogenic mechanisms in BrCa. Finally, we performed experimentally validated their oncogenic roles in BrCa. Overall, our findings systematically elucidate the expression and distinct prognostic value of 14-3-3 isoforms in BrCa, which may provide potential therapeutic targets and prognostic biomarkers for BrCa. |
format | Online Article Text |
id | pubmed-7732302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-77323022020-12-18 Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer Mei, Jie Liu, Yan Xu, Rui Hao, Leiyu Qin, An Chu, Chunqiang Zhu, Yichao Liu, Xiao Aging (Albany NY) Research Paper The tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation proteins (14-3-3) participate in the tumorigenesis and progression of numerous malignances, but their precise prognostic values in breast cancer (BrCa) remain unknown. Here, we investigated the expression profiles and prognostic roles of 14-3-3 isoforms by employing multiple online databases. The transcriptional levels of most 14-3-3 isoforms in BrCa tissues were significantly higher than those in normal tissues. High mRNA expression of 14-3-3 beta/sigma/theta/zeta was significantly associated with poor overall survival (OS) in BrCa patients, while high mRNA expression of 14-3-3 epsilon was notably related to favorable OS. High mRNA expression of 14-3-3 beta/gamma/sigma/theta/zeta was significantly associated with poor relapse-free survival (RFS) in BrCa patients. A high mutation rate of 14-3-3 was determined to be associated with poor clinical outcomes. In addition, 14-3-3 expression was correlated with the infiltration of specific immune cells types. Analysis of the breast-specific protein-protein interaction (PPI) network suggested that 14-3-3 proteins were involved in several potential oncogenic mechanisms in BrCa. Finally, we performed experimentally validated their oncogenic roles in BrCa. Overall, our findings systematically elucidate the expression and distinct prognostic value of 14-3-3 isoforms in BrCa, which may provide potential therapeutic targets and prognostic biomarkers for BrCa. Impact Journals 2020-10-14 /pmc/articles/PMC7732302/ /pubmed/33052135 http://dx.doi.org/10.18632/aging.103919 Text en Copyright: © 2020 Mei et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Mei, Jie Liu, Yan Xu, Rui Hao, Leiyu Qin, An Chu, Chunqiang Zhu, Yichao Liu, Xiao Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title | Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title_full | Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title_fullStr | Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title_full_unstemmed | Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title_short | Characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
title_sort | characterization of the expression and prognostic value of 14-3-3 isoforms in breast cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732302/ https://www.ncbi.nlm.nih.gov/pubmed/33052135 http://dx.doi.org/10.18632/aging.103919 |
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