Identification of potential immune-related prognostic biomarkers of lung cancer using gene co-expression network analysis

Objective The objective of this study was to identify new carcinogenetic hub genes and develop the integration of differentially expressed genes to predict the prognosis of lung cancer. Methods GSE139032 microarray data packages were downloaded from the Gene Expression Omnibus for planning, testing,...

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Veröffentlicht in:Oncology and translational medicine 2020-12, Vol.6 (6), p.247-257
Hauptverfasser: Chen, Aixia, Zhao, Shengnan, Zhou, Fei, Lv, Hongying, Liang, Donghai, Jiang, Tao, Liu, Rui, Zhu, Lijin, Cao, Jingyu, Liu, Shihai, Yu, Hongsheng
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container_end_page 257
container_issue 6
container_start_page 247
container_title Oncology and translational medicine
container_volume 6
creator Chen, Aixia
Zhao, Shengnan
Zhou, Fei
Lv, Hongying
Liang, Donghai
Jiang, Tao
Liu, Rui
Zhu, Lijin
Cao, Jingyu
Liu, Shihai
Yu, Hongsheng
description Objective The objective of this study was to identify new carcinogenetic hub genes and develop the integration of differentially expressed genes to predict the prognosis of lung cancer. Methods GSE139032 microarray data packages were downloaded from the Gene Expression Omnibus for planning, testing, and review of data. We identified KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV from a key module for validation. Results We found that the five genes were related to a poor prognosis, and the expression levels of these genes were associated with tumor stage. Furthermore, Kaplan-Meier plotter showed that the five hub genes had better prognostic values. The mean levels of methylation in lung adenocarcinoma (LUAD) were significantly lower than those in healthy lung tissues for the hub genes. However, gene set enrichment analysis (GSEA) for single hub genes showed that all of them were immune-related. Conclusion Our findings demonstrated that KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV are all candidate diagnostic and prognostic biomarkers for LUAD. They may have clinical implications in LUAD patients not only for the improvement of risk stratification but also for therapeutic decisions and prognosis prediction.
doi_str_mv 10.1007/s10330-020-0437-7
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Methods GSE139032 microarray data packages were downloaded from the Gene Expression Omnibus for planning, testing, and review of data. We identified KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV from a key module for validation. Results We found that the five genes were related to a poor prognosis, and the expression levels of these genes were associated with tumor stage. Furthermore, Kaplan-Meier plotter showed that the five hub genes had better prognostic values. The mean levels of methylation in lung adenocarcinoma (LUAD) were significantly lower than those in healthy lung tissues for the hub genes. However, gene set enrichment analysis (GSEA) for single hub genes showed that all of them were immune-related. Conclusion Our findings demonstrated that KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV are all candidate diagnostic and prognostic biomarkers for LUAD. 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All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c722-416dca3f52a4deb8eebbbf89ca0ae1597bc36ca7954ffdcf3f5c22a196707ffa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/dgyx/dgyx.jpg</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Chen, Aixia</creatorcontrib><creatorcontrib>Zhao, Shengnan</creatorcontrib><creatorcontrib>Zhou, Fei</creatorcontrib><creatorcontrib>Lv, Hongying</creatorcontrib><creatorcontrib>Liang, Donghai</creatorcontrib><creatorcontrib>Jiang, Tao</creatorcontrib><creatorcontrib>Liu, Rui</creatorcontrib><creatorcontrib>Zhu, Lijin</creatorcontrib><creatorcontrib>Cao, Jingyu</creatorcontrib><creatorcontrib>Liu, Shihai</creatorcontrib><creatorcontrib>Yu, Hongsheng</creatorcontrib><title>Identification of potential immune-related prognostic biomarkers of lung cancer using gene co-expression network analysis</title><title>Oncology and translational medicine</title><description>Objective The objective of this study was to identify new carcinogenetic hub genes and develop the integration of differentially expressed genes to predict the prognosis of lung cancer. Methods GSE139032 microarray data packages were downloaded from the Gene Expression Omnibus for planning, testing, and review of data. We identified KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV from a key module for validation. Results We found that the five genes were related to a poor prognosis, and the expression levels of these genes were associated with tumor stage. Furthermore, Kaplan-Meier plotter showed that the five hub genes had better prognostic values. The mean levels of methylation in lung adenocarcinoma (LUAD) were significantly lower than those in healthy lung tissues for the hub genes. However, gene set enrichment analysis (GSEA) for single hub genes showed that all of them were immune-related. Conclusion Our findings demonstrated that KRT6C, LAMC2, LAMB3, KRT6A, and MYEOV are all candidate diagnostic and prognostic biomarkers for LUAD. 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title Identification of potential immune-related prognostic biomarkers of lung cancer using gene co-expression network analysis
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