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Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis

Hepatocellular carcinoma (HCC) is still a significant global health problem. The development of bioinformatics may provide the opportunities to identify novel therapeutic targets. This study bioinformatically identified the differentially expressed genes (DEGs) in HCC and associated them with HCC pr...

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Autores principales: Huang, Xu, Wang, Xu, Huang, Ge, Li, Ruotao, Liu, Xingkai, Cao, Lidong, Ye, Junfeng, Zhang, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509045/
https://www.ncbi.nlm.nih.gov/pubmed/36197270
http://dx.doi.org/10.1097/MD.0000000000030678
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author Huang, Xu
Wang, Xu
Huang, Ge
Li, Ruotao
Liu, Xingkai
Cao, Lidong
Ye, Junfeng
Zhang, Ping
author_facet Huang, Xu
Wang, Xu
Huang, Ge
Li, Ruotao
Liu, Xingkai
Cao, Lidong
Ye, Junfeng
Zhang, Ping
author_sort Huang, Xu
collection PubMed
description Hepatocellular carcinoma (HCC) is still a significant global health problem. The development of bioinformatics may provide the opportunities to identify novel therapeutic targets. This study bioinformatically identified the differentially expressed genes (DEGs) in HCC and associated them with HCC prognosis using data from published databases. The DEGs downloaded from the Gene Expression Omnibus (GEO) website were visualized using the Venn diagram software, and then subjected to the GO and KEGG analyses, while the protein–protein interaction network was analyzed using Cytoscape software with the Search Tool for the search tool for the retrieval of interacting genes and the molecular complex detection plug-in. Kaplan–Meier curves and the log rank test were used to associate the core PPI network genes with the prognosis. There were 57 upregulated and 143 downregulated genes in HCC samples. The GO and pathway analyses revealed that these DEGs are involved in the biological processes (BPs), molecular functions (MFs), and cell components (CCs). The PPI network covered 50 upregulated and 108 downregulated genes, and the core modules of this PPI network contained 34 upregulated genes. A total of 28 of these upregulated genes were associated with a poor HCC prognosis, 27 of which were highly expressed in HCC tissues. This study identified 28 DEGs to be associated with a poor HCC prognosis. Future studies will investigate their possible applications as prognostic biomarkers and potential therapeutic targets for HCC.
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spelling pubmed-95090452022-09-26 Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis Huang, Xu Wang, Xu Huang, Ge Li, Ruotao Liu, Xingkai Cao, Lidong Ye, Junfeng Zhang, Ping Medicine (Baltimore) Research Article Hepatocellular carcinoma (HCC) is still a significant global health problem. The development of bioinformatics may provide the opportunities to identify novel therapeutic targets. This study bioinformatically identified the differentially expressed genes (DEGs) in HCC and associated them with HCC prognosis using data from published databases. The DEGs downloaded from the Gene Expression Omnibus (GEO) website were visualized using the Venn diagram software, and then subjected to the GO and KEGG analyses, while the protein–protein interaction network was analyzed using Cytoscape software with the Search Tool for the search tool for the retrieval of interacting genes and the molecular complex detection plug-in. Kaplan–Meier curves and the log rank test were used to associate the core PPI network genes with the prognosis. There were 57 upregulated and 143 downregulated genes in HCC samples. The GO and pathway analyses revealed that these DEGs are involved in the biological processes (BPs), molecular functions (MFs), and cell components (CCs). The PPI network covered 50 upregulated and 108 downregulated genes, and the core modules of this PPI network contained 34 upregulated genes. A total of 28 of these upregulated genes were associated with a poor HCC prognosis, 27 of which were highly expressed in HCC tissues. This study identified 28 DEGs to be associated with a poor HCC prognosis. Future studies will investigate their possible applications as prognostic biomarkers and potential therapeutic targets for HCC. Lippincott Williams & Wilkins 2022-09-23 /pmc/articles/PMC9509045/ /pubmed/36197270 http://dx.doi.org/10.1097/MD.0000000000030678 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Research Article
Huang, Xu
Wang, Xu
Huang, Ge
Li, Ruotao
Liu, Xingkai
Cao, Lidong
Ye, Junfeng
Zhang, Ping
Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title_full Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title_fullStr Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title_full_unstemmed Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title_short Bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
title_sort bioinformatic identification of differentially expressed genes associated with hepatocellular carcinoma prognosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509045/
https://www.ncbi.nlm.nih.gov/pubmed/36197270
http://dx.doi.org/10.1097/MD.0000000000030678
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