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KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway
BACKGROUND: Bladder cancer (BC) is the most common cancer of the urinary tract and invariably predicts a poor prognosis. In this study, we found a reliable gene signature and potential biomarker for predicting clinical prognosis. METHODS: The gene expression profiles were obtained from the GEO datab...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396666/ https://www.ncbi.nlm.nih.gov/pubmed/30881113 http://dx.doi.org/10.2147/CMAR.S191681 |
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author | Zhao, Hongda Bo, Qiyu Wu, Zonglong Liu, Qinggang Li, Yan Zhang, Ning Guo, Hu Shi, Benkang |
author_facet | Zhao, Hongda Bo, Qiyu Wu, Zonglong Liu, Qinggang Li, Yan Zhang, Ning Guo, Hu Shi, Benkang |
author_sort | Zhao, Hongda |
collection | PubMed |
description | BACKGROUND: Bladder cancer (BC) is the most common cancer of the urinary tract and invariably predicts a poor prognosis. In this study, we found a reliable gene signature and potential biomarker for predicting clinical prognosis. METHODS: The gene expression profiles were obtained from the GEO database. By performing GEO2R analysis, numerous differentially expressed genes (DEGs) were found. Three different microarray datasets were integrated in order to more precisely identify up-expression genes. Functional analysis revealed that these genes were mainly involved in cell cycle, DNA replication and metabolic pathways. RESULTS: Based on protein-protein interactome (PPI) networks that were identified in the current study and previous studies, we focused on KIF15 for further study. The results showed that KIF15 promotes BC cell proliferation via the MEK -ERK pathway, and Kaplan‐Meier survival analysis revealed that KIF15 expression was an independent prognostic risk factor in BC patients. CONCLUSION: KIF15 may represent a promising prognostic biomarker and a potential therapeutic option for BC. |
format | Online Article Text |
id | pubmed-6396666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63966662019-03-15 KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway Zhao, Hongda Bo, Qiyu Wu, Zonglong Liu, Qinggang Li, Yan Zhang, Ning Guo, Hu Shi, Benkang Cancer Manag Res Original Research BACKGROUND: Bladder cancer (BC) is the most common cancer of the urinary tract and invariably predicts a poor prognosis. In this study, we found a reliable gene signature and potential biomarker for predicting clinical prognosis. METHODS: The gene expression profiles were obtained from the GEO database. By performing GEO2R analysis, numerous differentially expressed genes (DEGs) were found. Three different microarray datasets were integrated in order to more precisely identify up-expression genes. Functional analysis revealed that these genes were mainly involved in cell cycle, DNA replication and metabolic pathways. RESULTS: Based on protein-protein interactome (PPI) networks that were identified in the current study and previous studies, we focused on KIF15 for further study. The results showed that KIF15 promotes BC cell proliferation via the MEK -ERK pathway, and Kaplan‐Meier survival analysis revealed that KIF15 expression was an independent prognostic risk factor in BC patients. CONCLUSION: KIF15 may represent a promising prognostic biomarker and a potential therapeutic option for BC. Dove Medical Press 2019-02-26 /pmc/articles/PMC6396666/ /pubmed/30881113 http://dx.doi.org/10.2147/CMAR.S191681 Text en © 2019 Zhao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zhao, Hongda Bo, Qiyu Wu, Zonglong Liu, Qinggang Li, Yan Zhang, Ning Guo, Hu Shi, Benkang KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title | KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title_full | KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title_fullStr | KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title_full_unstemmed | KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title_short | KIF15 promotes bladder cancer proliferation via the MEK–ERK signaling pathway |
title_sort | kif15 promotes bladder cancer proliferation via the mek–erk signaling pathway |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396666/ https://www.ncbi.nlm.nih.gov/pubmed/30881113 http://dx.doi.org/10.2147/CMAR.S191681 |
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