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Possible pathways used to predict different stages of lung adenocarcinoma
We aimed to find some specific pathways that can be used to predict the stage of lung adenocarcinoma. RNA-Seq expression profile data and clinical data of lung adenocarcinoma (stage I [37], stage II 161], stage III [75], and stage IV [45]) were obtained from the TCGA dataset. The differentially expr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413258/ https://www.ncbi.nlm.nih.gov/pubmed/28445293 http://dx.doi.org/10.1097/MD.0000000000006736 |
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author | Chen, Xiaodong Duan, Qiongyu Xuan, Ying Sun, Yunan Wu, Rong |
author_facet | Chen, Xiaodong Duan, Qiongyu Xuan, Ying Sun, Yunan Wu, Rong |
author_sort | Chen, Xiaodong |
collection | PubMed |
description | We aimed to find some specific pathways that can be used to predict the stage of lung adenocarcinoma. RNA-Seq expression profile data and clinical data of lung adenocarcinoma (stage I [37], stage II 161], stage III [75], and stage IV [45]) were obtained from the TCGA dataset. The differentially expressed genes were merged, correlation coefficient matrix between genes was constructed with correlation analysis, and unsupervised clustering was carried out with hierarchical clustering method. The specific coexpression network in every stage was constructed with cytoscape software. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis was performed with KOBAS database and Fisher exact test. Euclidean distance algorithm was used to calculate total deviation score. The diagnostic model was constructed with SVM algorithm. Eighteen specific genes were obtained by getting intersection of 4 group differentially expressed genes. Ten significantly enriched pathways were obtained. In the distribution map of 10 pathways score in different groups, degrees that sample groups deviated from the normal level were as follows: stage I < stage II < stage III < stage IV. The pathway score of 4 stages exhibited linear change in some pathways, and the score of 1 or 2 stages were significantly different from the rest stages in some pathways. There was significant difference between dead and alive for these pathways except thyroid hormone signaling pathway. Those 10 pathways are associated with the development of lung adenocarcinoma and may be able to predict different stages of it. Furthermore, these pathways except thyroid hormone signaling pathway may be able to predict the prognosis. |
format | Online Article Text |
id | pubmed-5413258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-54132582017-05-05 Possible pathways used to predict different stages of lung adenocarcinoma Chen, Xiaodong Duan, Qiongyu Xuan, Ying Sun, Yunan Wu, Rong Medicine (Baltimore) 5700 We aimed to find some specific pathways that can be used to predict the stage of lung adenocarcinoma. RNA-Seq expression profile data and clinical data of lung adenocarcinoma (stage I [37], stage II 161], stage III [75], and stage IV [45]) were obtained from the TCGA dataset. The differentially expressed genes were merged, correlation coefficient matrix between genes was constructed with correlation analysis, and unsupervised clustering was carried out with hierarchical clustering method. The specific coexpression network in every stage was constructed with cytoscape software. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis was performed with KOBAS database and Fisher exact test. Euclidean distance algorithm was used to calculate total deviation score. The diagnostic model was constructed with SVM algorithm. Eighteen specific genes were obtained by getting intersection of 4 group differentially expressed genes. Ten significantly enriched pathways were obtained. In the distribution map of 10 pathways score in different groups, degrees that sample groups deviated from the normal level were as follows: stage I < stage II < stage III < stage IV. The pathway score of 4 stages exhibited linear change in some pathways, and the score of 1 or 2 stages were significantly different from the rest stages in some pathways. There was significant difference between dead and alive for these pathways except thyroid hormone signaling pathway. Those 10 pathways are associated with the development of lung adenocarcinoma and may be able to predict different stages of it. Furthermore, these pathways except thyroid hormone signaling pathway may be able to predict the prognosis. Wolters Kluwer Health 2017-04-28 /pmc/articles/PMC5413258/ /pubmed/28445293 http://dx.doi.org/10.1097/MD.0000000000006736 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 5700 Chen, Xiaodong Duan, Qiongyu Xuan, Ying Sun, Yunan Wu, Rong Possible pathways used to predict different stages of lung adenocarcinoma |
title | Possible pathways used to predict different stages of lung adenocarcinoma |
title_full | Possible pathways used to predict different stages of lung adenocarcinoma |
title_fullStr | Possible pathways used to predict different stages of lung adenocarcinoma |
title_full_unstemmed | Possible pathways used to predict different stages of lung adenocarcinoma |
title_short | Possible pathways used to predict different stages of lung adenocarcinoma |
title_sort | possible pathways used to predict different stages of lung adenocarcinoma |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413258/ https://www.ncbi.nlm.nih.gov/pubmed/28445293 http://dx.doi.org/10.1097/MD.0000000000006736 |
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