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High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database
PURPOSE: Liver cancer is a high mortality disease with no curable treatments. Posttranscriptional modifications play essential roles in the occurrence and the progression of liver cancer. EIF2B5 is a subunit of EIF2B that regulates the initiation and the rate of translation and participates in sever...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255118/ https://www.ncbi.nlm.nih.gov/pubmed/30538549 http://dx.doi.org/10.2147/CMAR.S185459 |
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author | Jiao, Yan Fu, Zhuo Li, Yanqing Meng, Lingyu Liu, Yahui |
author_facet | Jiao, Yan Fu, Zhuo Li, Yanqing Meng, Lingyu Liu, Yahui |
author_sort | Jiao, Yan |
collection | PubMed |
description | PURPOSE: Liver cancer is a high mortality disease with no curable treatments. Posttranscriptional modifications play essential roles in the occurrence and the progression of liver cancer. EIF2B5 is a subunit of EIF2B that regulates the initiation and the rate of translation and participates in several diseases including tumors. This study aims to elucidate the prognostic significance of EIF2B5 in liver cancer. MATERIALS AND METHODS: We used The Cancer Genome Atlas database to analyze the expression of EIF2B5 in liver cancer. Then we used chi-squared and Fisher exact tests to test the correlation between clinical characteristics and EIF2B5 expression. Finally, we assessed the role of EIF2B5 in prognosis by Kaplan–Meier curves and Cox analysis. Gene set enrichment analysis was performed by using The Cancer Genome Atlas data set. RESULTS: The results showed that EIF2B5 was upregulated in liver cancer, and the expression was related to histologic grade, clinical stage, and vital status. Moreover, Kaplan–Meier curves and Cox analysis implicated that highly expressed EIF2B5 correlated with poor prognosis, and EIF2B5 was an independent risk factor for liver cancer. Gene set enrichment analysis showed that ATR and BRCA pathway, cell cycle pathway, DNA repair, myc signaling pathway, and E2F targets are differentially enriched in EIF2B5 high-expression phenotype. CONCLUSION: Our results suggest that EIF2B5 participated in cancer progression and could become a biomarker for the prognosis of patients with liver cancer. |
format | Online Article Text |
id | pubmed-6255118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62551182018-12-11 High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database Jiao, Yan Fu, Zhuo Li, Yanqing Meng, Lingyu Liu, Yahui Cancer Manag Res Original Research PURPOSE: Liver cancer is a high mortality disease with no curable treatments. Posttranscriptional modifications play essential roles in the occurrence and the progression of liver cancer. EIF2B5 is a subunit of EIF2B that regulates the initiation and the rate of translation and participates in several diseases including tumors. This study aims to elucidate the prognostic significance of EIF2B5 in liver cancer. MATERIALS AND METHODS: We used The Cancer Genome Atlas database to analyze the expression of EIF2B5 in liver cancer. Then we used chi-squared and Fisher exact tests to test the correlation between clinical characteristics and EIF2B5 expression. Finally, we assessed the role of EIF2B5 in prognosis by Kaplan–Meier curves and Cox analysis. Gene set enrichment analysis was performed by using The Cancer Genome Atlas data set. RESULTS: The results showed that EIF2B5 was upregulated in liver cancer, and the expression was related to histologic grade, clinical stage, and vital status. Moreover, Kaplan–Meier curves and Cox analysis implicated that highly expressed EIF2B5 correlated with poor prognosis, and EIF2B5 was an independent risk factor for liver cancer. Gene set enrichment analysis showed that ATR and BRCA pathway, cell cycle pathway, DNA repair, myc signaling pathway, and E2F targets are differentially enriched in EIF2B5 high-expression phenotype. CONCLUSION: Our results suggest that EIF2B5 participated in cancer progression and could become a biomarker for the prognosis of patients with liver cancer. Dove Medical Press 2018-11-20 /pmc/articles/PMC6255118/ /pubmed/30538549 http://dx.doi.org/10.2147/CMAR.S185459 Text en © 2018 Jiao 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 Jiao, Yan Fu, Zhuo Li, Yanqing Meng, Lingyu Liu, Yahui High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title | High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title_full | High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title_fullStr | High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title_full_unstemmed | High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title_short | High EIF2B5 mRNA expression and its prognostic significance in liver cancer: a study based on the TCGA and GEO database |
title_sort | high eif2b5 mrna expression and its prognostic significance in liver cancer: a study based on the tcga and geo database |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255118/ https://www.ncbi.nlm.nih.gov/pubmed/30538549 http://dx.doi.org/10.2147/CMAR.S185459 |
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