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Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis
BACKGROUND: Papillary thyroid carcinoma (PTC), which is the most common endocrine malignancy, has been steadily increasing worldwide in incidence over the years, while mechanisms underlying the pathogenesis and diagnostic for PTC are incomplete. The purpose of this study is to identify potential bio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7161219/ https://www.ncbi.nlm.nih.gov/pubmed/32299435 http://dx.doi.org/10.1186/s12967-020-02327-7 |
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author | Liu, Yang Chen, Ting-Yu Yang, Zhi-Yan Fang, Wei Wu, Qian Zhang, Chao |
author_facet | Liu, Yang Chen, Ting-Yu Yang, Zhi-Yan Fang, Wei Wu, Qian Zhang, Chao |
author_sort | Liu, Yang |
collection | PubMed |
description | BACKGROUND: Papillary thyroid carcinoma (PTC), which is the most common endocrine malignancy, has been steadily increasing worldwide in incidence over the years, while mechanisms underlying the pathogenesis and diagnostic for PTC are incomplete. The purpose of this study is to identify potential biomarkers for diagnosis of PTC, and provide new insights into pathogenesis of PTC. METHODS: Based on weighted gene co-expression network analysis, Robust Rank Aggregation, functional annotation, GSEA and DNA methylation, were employed for investigating potential biomarkers for diagnosis of PTC. RESULTS: Black and turquoise modules were identified in the gene co-expression network constructed by 1807 DEGs that from 6 eligible gene expression profiles of Gene Expression Omnibus database based on Robust Rank Aggregation and weighted gene co-expression network analysis. Hub genes were significantly down-regulated and the expression levels of the hub genes were different in different stages in hub gene verification. ROC curves indicated all hub genes had good diagnostic value for PTC (except for ABCA6 AUC = 89.5%, the 15 genes with AUC > 90%). Methylation analysis showed that hub gene verification ABCA6, ACACB, RMDN1 and TFPI were identified as differentially methylated genes, and the decreased expression level of these genes may relate to abnormal DNA methylation. Moreover, the expression levels of 8 top hub genes were correlated with tumor purity and tumor-infiltrating immune cells. These findings, including functional annotations and GSEA provide new insights into pathogenesis of PTC. CONCLUSIONS: The hub genes and methylation of hub genes may as potential biomarkers provide new insights for diagnosis of PTC, and all these findings may be the direction to study the mechanisms underlying of PTC in the future. |
format | Online Article Text |
id | pubmed-7161219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71612192020-04-22 Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis Liu, Yang Chen, Ting-Yu Yang, Zhi-Yan Fang, Wei Wu, Qian Zhang, Chao J Transl Med Research BACKGROUND: Papillary thyroid carcinoma (PTC), which is the most common endocrine malignancy, has been steadily increasing worldwide in incidence over the years, while mechanisms underlying the pathogenesis and diagnostic for PTC are incomplete. The purpose of this study is to identify potential biomarkers for diagnosis of PTC, and provide new insights into pathogenesis of PTC. METHODS: Based on weighted gene co-expression network analysis, Robust Rank Aggregation, functional annotation, GSEA and DNA methylation, were employed for investigating potential biomarkers for diagnosis of PTC. RESULTS: Black and turquoise modules were identified in the gene co-expression network constructed by 1807 DEGs that from 6 eligible gene expression profiles of Gene Expression Omnibus database based on Robust Rank Aggregation and weighted gene co-expression network analysis. Hub genes were significantly down-regulated and the expression levels of the hub genes were different in different stages in hub gene verification. ROC curves indicated all hub genes had good diagnostic value for PTC (except for ABCA6 AUC = 89.5%, the 15 genes with AUC > 90%). Methylation analysis showed that hub gene verification ABCA6, ACACB, RMDN1 and TFPI were identified as differentially methylated genes, and the decreased expression level of these genes may relate to abnormal DNA methylation. Moreover, the expression levels of 8 top hub genes were correlated with tumor purity and tumor-infiltrating immune cells. These findings, including functional annotations and GSEA provide new insights into pathogenesis of PTC. CONCLUSIONS: The hub genes and methylation of hub genes may as potential biomarkers provide new insights for diagnosis of PTC, and all these findings may be the direction to study the mechanisms underlying of PTC in the future. BioMed Central 2020-04-16 /pmc/articles/PMC7161219/ /pubmed/32299435 http://dx.doi.org/10.1186/s12967-020-02327-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Yang Chen, Ting-Yu Yang, Zhi-Yan Fang, Wei Wu, Qian Zhang, Chao Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title | Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title_full | Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title_fullStr | Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title_full_unstemmed | Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title_short | Identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
title_sort | identification of hub genes in papillary thyroid carcinoma: robust rank aggregation and weighted gene co-expression network analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7161219/ https://www.ncbi.nlm.nih.gov/pubmed/32299435 http://dx.doi.org/10.1186/s12967-020-02327-7 |
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