Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer

Abstract To screen the key genes in the development of gastric cancer and their influence on prognosis. The GEO database was used to screen gastric cancer-related gene chips as a training set, and the R packages limma tool was used to analyze the differential genes expressed in gastric cancer tissue...

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Autores principales: Jiasheng Xu, Xinlu Wang, Qiwen Ke, Kaili Liao, Yanhua Wan, Kaihua Zhang, Guanyu Zhang, Xiaozhong Wang
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/563d454a00a3492c9fcc0bfdd493674a
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spelling oai:doaj.org-article:563d454a00a3492c9fcc0bfdd493674a2021-12-02T16:31:47ZCombined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer10.1038/s41598-021-94291-52045-2322https://doaj.org/article/563d454a00a3492c9fcc0bfdd493674a2021-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-94291-5https://doaj.org/toc/2045-2322Abstract To screen the key genes in the development of gastric cancer and their influence on prognosis. The GEO database was used to screen gastric cancer-related gene chips as a training set, and the R packages limma tool was used to analyze the differential genes expressed in gastric cancer tissues compared to normal tissues, and then the selected genes were verified in the validation set. The String database was used to calculate their Protein–protein interaction (PPI) network, using Cytoscape software's Centiscape and other plug-ins to analyze key genes in the PPI network. The DAVID database was used to enrich and annotate gene functions of differential genes and PPI key module genes, and further explore correlation between expression level and clinical stage and prognosis. Based on clinical data and patient samples, differential expression of key node genes was verified by immunohistochemistry. The 63 characteristic differential genes screened had good discrimination between gastric cancer and normal tissues, and are mainly involved in regulating extracellular matrix receptor interactions and the PI3k-AKT signaling pathway. Key nodes in the PPI network regulate tumor proliferation and metastasis. Analysis of the expression levels of key node genes found that relative to normal tissues, the expression of ITGB1 and COL1A2 was significantly increased in gastric cancer tissues, and patients with late clinical stages of tumors had higher expression of ITGB1 and COL1A2 in tumor tissues, and their survival time was longer (P < 0.05). This study found that ITGB1 and COL1A2 are key genes in the development of gastric cancer and can be used as prognostic markers and potential new targets for gastric cancer.Jiasheng XuXinlu WangQiwen KeKaili LiaoYanhua WanKaihua ZhangGuanyu ZhangXiaozhong WangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jiasheng Xu
Xinlu Wang
Qiwen Ke
Kaili Liao
Yanhua Wan
Kaihua Zhang
Guanyu Zhang
Xiaozhong Wang
Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
description Abstract To screen the key genes in the development of gastric cancer and their influence on prognosis. The GEO database was used to screen gastric cancer-related gene chips as a training set, and the R packages limma tool was used to analyze the differential genes expressed in gastric cancer tissues compared to normal tissues, and then the selected genes were verified in the validation set. The String database was used to calculate their Protein–protein interaction (PPI) network, using Cytoscape software's Centiscape and other plug-ins to analyze key genes in the PPI network. The DAVID database was used to enrich and annotate gene functions of differential genes and PPI key module genes, and further explore correlation between expression level and clinical stage and prognosis. Based on clinical data and patient samples, differential expression of key node genes was verified by immunohistochemistry. The 63 characteristic differential genes screened had good discrimination between gastric cancer and normal tissues, and are mainly involved in regulating extracellular matrix receptor interactions and the PI3k-AKT signaling pathway. Key nodes in the PPI network regulate tumor proliferation and metastasis. Analysis of the expression levels of key node genes found that relative to normal tissues, the expression of ITGB1 and COL1A2 was significantly increased in gastric cancer tissues, and patients with late clinical stages of tumors had higher expression of ITGB1 and COL1A2 in tumor tissues, and their survival time was longer (P < 0.05). This study found that ITGB1 and COL1A2 are key genes in the development of gastric cancer and can be used as prognostic markers and potential new targets for gastric cancer.
format article
author Jiasheng Xu
Xinlu Wang
Qiwen Ke
Kaili Liao
Yanhua Wan
Kaihua Zhang
Guanyu Zhang
Xiaozhong Wang
author_facet Jiasheng Xu
Xinlu Wang
Qiwen Ke
Kaili Liao
Yanhua Wan
Kaihua Zhang
Guanyu Zhang
Xiaozhong Wang
author_sort Jiasheng Xu
title Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
title_short Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
title_full Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
title_fullStr Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
title_full_unstemmed Combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
title_sort combined bioinformatics technology to explore pivot genes and related clinical prognosis in the development of gastric cancer
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/563d454a00a3492c9fcc0bfdd493674a
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