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Identification of potential hub genes of gastric cancer
Gastric cancer (GC) is a malignant tumor originated from gastric mucosa epithelium. It is the third leading cause of cancer mortality in China. The early symptoms are not obvious. When it is discovered, it has developed to the advanced stage, and the prognosis is poor. In order to screen for potenti...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575828/ https://www.ncbi.nlm.nih.gov/pubmed/36254003 http://dx.doi.org/10.1097/MD.0000000000030741 |
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author | Zhou, Xu-Dong Qu, Ya-Wei Wang, Li Jia, Fu-Hua Chen, Peng Wang, Yin-Pu Liu, Hai-Feng |
author_facet | Zhou, Xu-Dong Qu, Ya-Wei Wang, Li Jia, Fu-Hua Chen, Peng Wang, Yin-Pu Liu, Hai-Feng |
author_sort | Zhou, Xu-Dong |
collection | PubMed |
description | Gastric cancer (GC) is a malignant tumor originated from gastric mucosa epithelium. It is the third leading cause of cancer mortality in China. The early symptoms are not obvious. When it is discovered, it has developed to the advanced stage, and the prognosis is poor. In order to screen for potential genes for GC development, this study obtained GSE118916 and GSE109476 from the gene expression omnibus (GEO) database for bioinformatics analysis. METHODS: First, GEO2R was used to identify differentially expressed genes (DEG) and the functional annotation of DEGs was performed by gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. The Search Tool for the Retrieval of Interacting Genes (STRING) tool was used to construct protein-protein interaction (PPI) network and the most important modules and hub genes were mined. Real time quantitative polymerase chain reaction assay was performed to verify the expression level of hub genes. RESULTS: A total of 139 DEGs were identified. The functional changes of DEGs are mainly concentrated in the cytoskeleton, extracellular matrix and collagen synthesis. Eleven genes were identified as core genes. Bioinformatics analysis shows that the core genes are mainly enriched in many processes related to cell adhesion and collagen. CONCLUSION: In summary, the DEGs and hub genes found in this study may be potential diagnostic and therapeutic targets. |
format | Online Article Text |
id | pubmed-9575828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-95758282022-10-17 Identification of potential hub genes of gastric cancer Zhou, Xu-Dong Qu, Ya-Wei Wang, Li Jia, Fu-Hua Chen, Peng Wang, Yin-Pu Liu, Hai-Feng Medicine (Baltimore) 4500 Gastric cancer (GC) is a malignant tumor originated from gastric mucosa epithelium. It is the third leading cause of cancer mortality in China. The early symptoms are not obvious. When it is discovered, it has developed to the advanced stage, and the prognosis is poor. In order to screen for potential genes for GC development, this study obtained GSE118916 and GSE109476 from the gene expression omnibus (GEO) database for bioinformatics analysis. METHODS: First, GEO2R was used to identify differentially expressed genes (DEG) and the functional annotation of DEGs was performed by gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. The Search Tool for the Retrieval of Interacting Genes (STRING) tool was used to construct protein-protein interaction (PPI) network and the most important modules and hub genes were mined. Real time quantitative polymerase chain reaction assay was performed to verify the expression level of hub genes. RESULTS: A total of 139 DEGs were identified. The functional changes of DEGs are mainly concentrated in the cytoskeleton, extracellular matrix and collagen synthesis. Eleven genes were identified as core genes. Bioinformatics analysis shows that the core genes are mainly enriched in many processes related to cell adhesion and collagen. CONCLUSION: In summary, the DEGs and hub genes found in this study may be potential diagnostic and therapeutic targets. Lippincott Williams & Wilkins 2022-10-14 /pmc/articles/PMC9575828/ /pubmed/36254003 http://dx.doi.org/10.1097/MD.0000000000030741 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 | 4500 Zhou, Xu-Dong Qu, Ya-Wei Wang, Li Jia, Fu-Hua Chen, Peng Wang, Yin-Pu Liu, Hai-Feng Identification of potential hub genes of gastric cancer |
title | Identification of potential hub genes of gastric cancer |
title_full | Identification of potential hub genes of gastric cancer |
title_fullStr | Identification of potential hub genes of gastric cancer |
title_full_unstemmed | Identification of potential hub genes of gastric cancer |
title_short | Identification of potential hub genes of gastric cancer |
title_sort | identification of potential hub genes of gastric cancer |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575828/ https://www.ncbi.nlm.nih.gov/pubmed/36254003 http://dx.doi.org/10.1097/MD.0000000000030741 |
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