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Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma
BACKGROUND: Adrenocortical carcinoma (ACC) is a malignant tumor with poor prognosis and unclear pathogenesis. This study aimed to explore the role of long non-coding RNAs (lncRNAs) in ACC. METHODS: We obtained the lncRNA expression profiles of 10 ACC samples and 6 normal control samples from the GEO...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798464/ https://www.ncbi.nlm.nih.gov/pubmed/35116967 http://dx.doi.org/10.21037/tcr.2019.09.34 |
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author | Zhou, Yang Wang, Xiao Zhu, Xi Liu, Fang-Chen Ye, Feng Wu, Dan-Hong Zhong, Ping |
author_facet | Zhou, Yang Wang, Xiao Zhu, Xi Liu, Fang-Chen Ye, Feng Wu, Dan-Hong Zhong, Ping |
author_sort | Zhou, Yang |
collection | PubMed |
description | BACKGROUND: Adrenocortical carcinoma (ACC) is a malignant tumor with poor prognosis and unclear pathogenesis. This study aimed to explore the role of long non-coding RNAs (lncRNAs) in ACC. METHODS: We obtained the lncRNA expression profiles of 10 ACC samples and 6 normal control samples from the GEO database and identified differentially expressed RNAs using the limma package in R. RESULTS: We obtained a total of 391 differentially expressed lncRNAs (DElncRNAs) and 1,313 differentially expressed mRNAs (DEmRNAs) between ACC samples and normal control samples. Using Cytoscape v3.7.0, we then constructed a lncRNA-miRNA-mRNA (competing endogenous RNA, or ceRNA) network consisting of 87 lncRNAs, 31 miRNAs, and 78 mRNAs. Applying GO and KEGG enrichment analysis for 78 mRNAs in the ceRNA network, we identified 9 GO terms and 21 significantly enriched pathways. A PPI network was constructed using STRING online tools and Cytoscape v3.7.0, identifying 10 key genes. Finally, through Kaplan-Meier survival analysis, we identified five lncRNAs (LINC00887, MEIS1-AS2, MIR29B2CHG, MIR503HG, and SREBF2-AS1) associated with prognosis in patients with ACC. CONCLUSIONS: In summary, we constructed a ceRNA network and propose a new method for lncRNA research in ACC. Our results provide new clues for further exploration of lncRNAs in the pathogenesis of ACC. |
format | Online Article Text |
id | pubmed-8798464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87984642022-02-02 Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma Zhou, Yang Wang, Xiao Zhu, Xi Liu, Fang-Chen Ye, Feng Wu, Dan-Hong Zhong, Ping Transl Cancer Res Original Article BACKGROUND: Adrenocortical carcinoma (ACC) is a malignant tumor with poor prognosis and unclear pathogenesis. This study aimed to explore the role of long non-coding RNAs (lncRNAs) in ACC. METHODS: We obtained the lncRNA expression profiles of 10 ACC samples and 6 normal control samples from the GEO database and identified differentially expressed RNAs using the limma package in R. RESULTS: We obtained a total of 391 differentially expressed lncRNAs (DElncRNAs) and 1,313 differentially expressed mRNAs (DEmRNAs) between ACC samples and normal control samples. Using Cytoscape v3.7.0, we then constructed a lncRNA-miRNA-mRNA (competing endogenous RNA, or ceRNA) network consisting of 87 lncRNAs, 31 miRNAs, and 78 mRNAs. Applying GO and KEGG enrichment analysis for 78 mRNAs in the ceRNA network, we identified 9 GO terms and 21 significantly enriched pathways. A PPI network was constructed using STRING online tools and Cytoscape v3.7.0, identifying 10 key genes. Finally, through Kaplan-Meier survival analysis, we identified five lncRNAs (LINC00887, MEIS1-AS2, MIR29B2CHG, MIR503HG, and SREBF2-AS1) associated with prognosis in patients with ACC. CONCLUSIONS: In summary, we constructed a ceRNA network and propose a new method for lncRNA research in ACC. Our results provide new clues for further exploration of lncRNAs in the pathogenesis of ACC. AME Publishing Company 2019-09 /pmc/articles/PMC8798464/ /pubmed/35116967 http://dx.doi.org/10.21037/tcr.2019.09.34 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Zhou, Yang Wang, Xiao Zhu, Xi Liu, Fang-Chen Ye, Feng Wu, Dan-Hong Zhong, Ping Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title | Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title_full | Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title_fullStr | Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title_full_unstemmed | Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title_short | Bioinformatic analysis of long non-coding RNA-associated competing endogenous RNA network in adrenocortical carcinoma |
title_sort | bioinformatic analysis of long non-coding rna-associated competing endogenous rna network in adrenocortical carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798464/ https://www.ncbi.nlm.nih.gov/pubmed/35116967 http://dx.doi.org/10.21037/tcr.2019.09.34 |
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