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The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC

OBJECTIVE: To investigate the value of CEP55 as a diagnostic marker and independent prognostic factor in lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC), and to analyze its co-expression genes and related signaling pathways. METHODS: TCGA database and GEO database were used to analyze...

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Autores principales: Fu, Linhai, Wang, Haiyong, Wei, Desheng, Wang, Bin, Zhang, Chu, Zhu, Ting, Ma, Zhifeng, Li, Zhupeng, Wu, Yuanlin, Yu, Guangmao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241791/
https://www.ncbi.nlm.nih.gov/pubmed/32437446
http://dx.doi.org/10.1371/journal.pone.0233283
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author Fu, Linhai
Wang, Haiyong
Wei, Desheng
Wang, Bin
Zhang, Chu
Zhu, Ting
Ma, Zhifeng
Li, Zhupeng
Wu, Yuanlin
Yu, Guangmao
author_facet Fu, Linhai
Wang, Haiyong
Wei, Desheng
Wang, Bin
Zhang, Chu
Zhu, Ting
Ma, Zhifeng
Li, Zhupeng
Wu, Yuanlin
Yu, Guangmao
author_sort Fu, Linhai
collection PubMed
description OBJECTIVE: To investigate the value of CEP55 as a diagnostic marker and independent prognostic factor in lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC), and to analyze its co-expression genes and related signaling pathways. METHODS: TCGA database and GEO database were used to analyze the expression of CEP55 in LUAD and LUSC compared with normal tissues. The co-expression genes of CEP55 in LUAD and LUSC were excavated by cBioPortal and enriched by KEGG and GO. Establishing Receiver operating characteristic (ROC) curve to evaluate the value of CEP55 as a diagnostic and prognostic factor. The association between CEP55 expression and the clinicopathological features was evaluated using χ2 tests. ROC curves for diagnosis and prognosis detection were constructed. Prognostic values were analyzed by univariate and multivariate Cox regression models. RESULTS: Compared with normal lung tissues, CEP55 expression was significantly upregulated in both LUAD and LUSC. ROC curve analysis showed that CEP55 could be used as an effective diagnostic target for LUAD (AUC = 0.969) and LUSC (AUC = 0.994). When CEP55 gene was selected as an independent prognostic factor, high expression of CEP55 was more disadvantageous to OS and RFS of LUAD patients (P<0.05), but no significant difference was found in LUSC patients (P>0.05). The number of co-expression genes of CEP55 in LUAD is more than that in LUSC, and is related to cell cycle, DNA replication and P53 signaling pathway. CONCLUSION: CEP55 can be used as a diagnostic marker for LUAD and LUSC, but only as an independent prognostic factor for LUAD rather than LUSC.
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spelling pubmed-72417912020-06-03 The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC Fu, Linhai Wang, Haiyong Wei, Desheng Wang, Bin Zhang, Chu Zhu, Ting Ma, Zhifeng Li, Zhupeng Wu, Yuanlin Yu, Guangmao PLoS One Research Article OBJECTIVE: To investigate the value of CEP55 as a diagnostic marker and independent prognostic factor in lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC), and to analyze its co-expression genes and related signaling pathways. METHODS: TCGA database and GEO database were used to analyze the expression of CEP55 in LUAD and LUSC compared with normal tissues. The co-expression genes of CEP55 in LUAD and LUSC were excavated by cBioPortal and enriched by KEGG and GO. Establishing Receiver operating characteristic (ROC) curve to evaluate the value of CEP55 as a diagnostic and prognostic factor. The association between CEP55 expression and the clinicopathological features was evaluated using χ2 tests. ROC curves for diagnosis and prognosis detection were constructed. Prognostic values were analyzed by univariate and multivariate Cox regression models. RESULTS: Compared with normal lung tissues, CEP55 expression was significantly upregulated in both LUAD and LUSC. ROC curve analysis showed that CEP55 could be used as an effective diagnostic target for LUAD (AUC = 0.969) and LUSC (AUC = 0.994). When CEP55 gene was selected as an independent prognostic factor, high expression of CEP55 was more disadvantageous to OS and RFS of LUAD patients (P<0.05), but no significant difference was found in LUSC patients (P>0.05). The number of co-expression genes of CEP55 in LUAD is more than that in LUSC, and is related to cell cycle, DNA replication and P53 signaling pathway. CONCLUSION: CEP55 can be used as a diagnostic marker for LUAD and LUSC, but only as an independent prognostic factor for LUAD rather than LUSC. Public Library of Science 2020-05-21 /pmc/articles/PMC7241791/ /pubmed/32437446 http://dx.doi.org/10.1371/journal.pone.0233283 Text en © 2020 Fu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fu, Linhai
Wang, Haiyong
Wei, Desheng
Wang, Bin
Zhang, Chu
Zhu, Ting
Ma, Zhifeng
Li, Zhupeng
Wu, Yuanlin
Yu, Guangmao
The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title_full The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title_fullStr The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title_full_unstemmed The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title_short The value of CEP55 gene as a diagnostic biomarker and independent prognostic factor in LUAD and LUSC
title_sort value of cep55 gene as a diagnostic biomarker and independent prognostic factor in luad and lusc
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241791/
https://www.ncbi.nlm.nih.gov/pubmed/32437446
http://dx.doi.org/10.1371/journal.pone.0233283
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