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Identification of hub genes and outcome in colon cancer based on bioinformatics analysis

BACKGROUND: Colon cancer is one of the leading malignant neoplasms worldwide. Until now, the concrete mechanisms of colonic cancerogenesis are largely unknown; identification of driven genes and pathways is, therefore, of great importance for monitoring and conquering this disease. This study aims t...

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Autores principales: Yang, Wanli, Ma, Jiaojiao, Zhou, Wei, Li, Zichao, Zhou, Xin, Cao, Bo, Zhang, Yujie, Liu, Jinqiang, Yang, Zhiping, Zhang, Hongwei, Zhao, Qingchuan, Hong, Liu, Fan, Daiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312054/
https://www.ncbi.nlm.nih.gov/pubmed/30643458
http://dx.doi.org/10.2147/CMAR.S173240
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author Yang, Wanli
Ma, Jiaojiao
Zhou, Wei
Li, Zichao
Zhou, Xin
Cao, Bo
Zhang, Yujie
Liu, Jinqiang
Yang, Zhiping
Zhang, Hongwei
Zhao, Qingchuan
Hong, Liu
Fan, Daiming
author_facet Yang, Wanli
Ma, Jiaojiao
Zhou, Wei
Li, Zichao
Zhou, Xin
Cao, Bo
Zhang, Yujie
Liu, Jinqiang
Yang, Zhiping
Zhang, Hongwei
Zhao, Qingchuan
Hong, Liu
Fan, Daiming
author_sort Yang, Wanli
collection PubMed
description BACKGROUND: Colon cancer is one of the leading malignant neoplasms worldwide. Until now, the concrete mechanisms of colonic cancerogenesis are largely unknown; identification of driven genes and pathways is, therefore, of great importance for monitoring and conquering this disease. This study aims to explore the potential biomarkers and therapeutic targets for colon cancer treatment. METHODS: The gene expression profile of GSE44076 from Gene Expression Omnibus database, including 98 primary colon cancers and 98 normal distant colon mucosa, was deeply analyzed. GEO2R tool was used to screen the differentially expressed genes (DEGs) between colon cancer tissues and normal samples. Gene Ontology analysis and Kyoto Encyclopedia of Genes and Genomes pathway analysis were performed for screening DEGs using Database for Annotation, Visualization and Integrated Discovery database and Panther database. Moreover, Search Tool for the Retrieval of Interacting Genes, Cytoscape software, and Molecular Complex Detection plug-in were used to visualize the protein–protein interaction of these DEGs. RESULTS: A total of 497 DEGs were obtained, including 129 upregulated genes mainly enriched in Hippo signaling pathway, Wnt signaling pathway, and cytokine–cytokine receptor interaction and 368 downregulated genes enriched in retinol metabolism, steroid hormone biosynthesis, drug metabolism, and chemical carcinogenesis. Using Molecular Complex Detection software, three important modules were selected from the protein–protein interaction network. Moreover, 20 hub genes with high degree of connectivity were selected, including COL1A1, CXCL5, GNG4, TIMP1, and so on. The Kaplan–Meier analysis for overall survival and correlation analysis were applied among the hub genes. CONCLUSION: Taken together, DEGs, especially the hub genes such as COL1A1, might be the driven genes in colon cancer progression. More importantly, they might be the novel biomarkers for diagnosis and guiding therapeutic strategies of colon cancer.
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spelling pubmed-63120542019-01-14 Identification of hub genes and outcome in colon cancer based on bioinformatics analysis Yang, Wanli Ma, Jiaojiao Zhou, Wei Li, Zichao Zhou, Xin Cao, Bo Zhang, Yujie Liu, Jinqiang Yang, Zhiping Zhang, Hongwei Zhao, Qingchuan Hong, Liu Fan, Daiming Cancer Manag Res Original Research BACKGROUND: Colon cancer is one of the leading malignant neoplasms worldwide. Until now, the concrete mechanisms of colonic cancerogenesis are largely unknown; identification of driven genes and pathways is, therefore, of great importance for monitoring and conquering this disease. This study aims to explore the potential biomarkers and therapeutic targets for colon cancer treatment. METHODS: The gene expression profile of GSE44076 from Gene Expression Omnibus database, including 98 primary colon cancers and 98 normal distant colon mucosa, was deeply analyzed. GEO2R tool was used to screen the differentially expressed genes (DEGs) between colon cancer tissues and normal samples. Gene Ontology analysis and Kyoto Encyclopedia of Genes and Genomes pathway analysis were performed for screening DEGs using Database for Annotation, Visualization and Integrated Discovery database and Panther database. Moreover, Search Tool for the Retrieval of Interacting Genes, Cytoscape software, and Molecular Complex Detection plug-in were used to visualize the protein–protein interaction of these DEGs. RESULTS: A total of 497 DEGs were obtained, including 129 upregulated genes mainly enriched in Hippo signaling pathway, Wnt signaling pathway, and cytokine–cytokine receptor interaction and 368 downregulated genes enriched in retinol metabolism, steroid hormone biosynthesis, drug metabolism, and chemical carcinogenesis. Using Molecular Complex Detection software, three important modules were selected from the protein–protein interaction network. Moreover, 20 hub genes with high degree of connectivity were selected, including COL1A1, CXCL5, GNG4, TIMP1, and so on. The Kaplan–Meier analysis for overall survival and correlation analysis were applied among the hub genes. CONCLUSION: Taken together, DEGs, especially the hub genes such as COL1A1, might be the driven genes in colon cancer progression. More importantly, they might be the novel biomarkers for diagnosis and guiding therapeutic strategies of colon cancer. Dove Medical Press 2018-12-27 /pmc/articles/PMC6312054/ /pubmed/30643458 http://dx.doi.org/10.2147/CMAR.S173240 Text en © 2019 Yang 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
Yang, Wanli
Ma, Jiaojiao
Zhou, Wei
Li, Zichao
Zhou, Xin
Cao, Bo
Zhang, Yujie
Liu, Jinqiang
Yang, Zhiping
Zhang, Hongwei
Zhao, Qingchuan
Hong, Liu
Fan, Daiming
Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title_full Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title_fullStr Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title_full_unstemmed Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title_short Identification of hub genes and outcome in colon cancer based on bioinformatics analysis
title_sort identification of hub genes and outcome in colon cancer based on bioinformatics analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312054/
https://www.ncbi.nlm.nih.gov/pubmed/30643458
http://dx.doi.org/10.2147/CMAR.S173240
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