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Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA)
Osteosarcoma (OS), the most common malignant bone tumor, accounts for the heavy healthy threat in the period of children and adolescents. OS occurrence usually correlates with early metastasis and high death rate. This study aimed to better understand the mechanism of OS metastasis. Based on Gene Ex...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023727/ https://www.ncbi.nlm.nih.gov/pubmed/29901575 http://dx.doi.org/10.1097/MD.0000000000010781 |
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author | Tian, Honglai Guan, Donghui Li, Jianmin |
author_facet | Tian, Honglai Guan, Donghui Li, Jianmin |
author_sort | Tian, Honglai |
collection | PubMed |
description | Osteosarcoma (OS), the most common malignant bone tumor, accounts for the heavy healthy threat in the period of children and adolescents. OS occurrence usually correlates with early metastasis and high death rate. This study aimed to better understand the mechanism of OS metastasis. Based on Gene Expression Omnibus (GEO) database, we downloaded 4 expression profile data sets associated with OS metastasis, and selected differential expressed genes. Weighted gene co-expression network analysis (WGCNA) approach allowed us to investigate the most OS metastasis-correlated module. Gene Ontology functional and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were used to give annotation of selected OS metastasis-associated genes. We select 897 differential expressed genes from OS metastasis and OS non-metastasis groups. Based on these selected genes, WGCNA further explored 142 genes included in the most OS metastasis-correlated module. Gene Ontology functional and KEGG pathway enrichment analyses showed that significantly OS metastasis-associated genes were involved in pathway correlated with insulin-like growth factor binding. Our research figured out several potential molecules participating in metastasis process and factors acting as biomarker. With this study, we could better explore the mechanism of OS metastasis and further discover more therapy targets. |
format | Online Article Text |
id | pubmed-6023727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-60237272018-07-03 Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) Tian, Honglai Guan, Donghui Li, Jianmin Medicine (Baltimore) Research Article Osteosarcoma (OS), the most common malignant bone tumor, accounts for the heavy healthy threat in the period of children and adolescents. OS occurrence usually correlates with early metastasis and high death rate. This study aimed to better understand the mechanism of OS metastasis. Based on Gene Expression Omnibus (GEO) database, we downloaded 4 expression profile data sets associated with OS metastasis, and selected differential expressed genes. Weighted gene co-expression network analysis (WGCNA) approach allowed us to investigate the most OS metastasis-correlated module. Gene Ontology functional and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were used to give annotation of selected OS metastasis-associated genes. We select 897 differential expressed genes from OS metastasis and OS non-metastasis groups. Based on these selected genes, WGCNA further explored 142 genes included in the most OS metastasis-correlated module. Gene Ontology functional and KEGG pathway enrichment analyses showed that significantly OS metastasis-associated genes were involved in pathway correlated with insulin-like growth factor binding. Our research figured out several potential molecules participating in metastasis process and factors acting as biomarker. With this study, we could better explore the mechanism of OS metastasis and further discover more therapy targets. Wolters Kluwer Health 2018-06-15 /pmc/articles/PMC6023727/ /pubmed/29901575 http://dx.doi.org/10.1097/MD.0000000000010781 Text en Copyright © 2018 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 | Research Article Tian, Honglai Guan, Donghui Li, Jianmin Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title | Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title_full | Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title_fullStr | Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title_full_unstemmed | Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title_short | Identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (WGCNA) |
title_sort | identifying osteosarcoma metastasis associated genes by weighted gene co-expression network analysis (wgcna) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023727/ https://www.ncbi.nlm.nih.gov/pubmed/29901575 http://dx.doi.org/10.1097/MD.0000000000010781 |
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