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pmid:35116364

Reconstruction and analysis of the aberrant lncRNA-miRNA-mRNA network based on competitive endogenous RNA in adenoid cystic carcinoma of the salivary gland.

Yu-Fang Tang · Wen-Jie Wu · Jian-Yun Zhang · Jie Zhang

Translational cancer research · 2021 doi:10.21037/tcr-21-1771

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Reconstruction and analysis of the aberrant lncRNA-miRNA-mRNA network based on competitive endogenous RNA in adenoid cystic carcinoma of the salivary gland.
doi
10.21037/tcr-21-1771
pmid
35116364
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[0]
Yu-Fang Tang
[1]
Wen-Jie Wu
[2]
Jian-Yun Zhang
[3]
Jie Zhang
journal
Translational cancer research
year
2021
abstract
BACKGROUND: The aim of this work was to investigate the competing endogenous RNA (ceRNA) network in adenoid cystic carcinoma of the salivary gland (SACC). METHODS: Differentially expressed lncRNAs (DElncRNAs), miRNAs (DEmiRNAs), and mRNAs (DEmRNAs) between cancer tissues and normal salivary gland (NSG) in ACC were identified using data from the Gene Expression Omnibus (GEO) database. Functional annotation and pathway enrichment analysis of DEmRNAs were performed using the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. The miRNAs that are targeted by lncRNAs were predicted using miRanda and PITA, while the target mRNAs of miRNAs were retrieved from miRanda, miRWalk, and TargetScan. A protein-protein interaction (PPI) network was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database, and then we constructed the lncRNA-miRNA-mRNA networks of ACC. RESULTS: Differentially expressed RNAs were identified in SACC. Upon comparing cancer tissues and NSG tissues, 103 upregulated and 52 downregulated lncRNAs and 745 upregulated and 866 downregulated mRNAs were identified in GSE88804; in addition, 39 upregulated and 43 downregulated miRNAs were identified in GSE117275. GO enrichment analyses revealed that the most relevant GO terms were regulation of transcription DNA-templated, transcription DNA-templated, and cell division. KEGG pathway enrichment analysis showed that differentially expressed genes (DEGs) were mainly enriched in the cell cycle, pathways in cancer, PI3K-Akt signaling pathway, breast cancer, and microRNAs in cancer. The PPI network consisted of 27 upregulated and 54 downregulated mRNAs. By constructing ceRNA network, NONHSAT251752.1-hsa-miR-6817-5p-NOTCH1, NONHSAT251752.1-hsa-miR-204-5p/hsa-miR-138-5p-CDK6 regulatory axises were identified and all genes in the network were verified by qRT-PCR. CONCLUSIONS: The present study constructed ceRNA networks in SACC and provided a novel perspective of the molecular mechanisms for SACC.
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The Edge R package in R (version 3.4.1) was used to identify the differentially expressed RNAs (DE-RNAs) (20).
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Through representational difference analysis, we identified 1,611 DE-mRNAs (745 up-regulated and 866 down-regulated), 155 DE-lncRNAs (103 up-regulated and 52 down-regulated), and 82 DE-miRNAs (39 up-regulated and 43 down-regulated).
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Through representational difference analysis, we identified 1,611 DE-mRNAs (745 up-regulated and 866 down-regulated), 155 DE-lncRNAs (103 up-regulated and 52 down-regulated), and 82 DE-miRNAs (39 up-regulated and 43 down-regulated).
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Through representational difference analysis, we identified 1,611 DE-mRNAs (745 up-regulated and 866 down-regulated), 155 DE-lncRNAs (103 up-regulated and 52 down-regulated), and 82 DE-miRNAs (39 up-regulated and 43 down-regulated).
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Functional annotation and pathway enrichment analysis of DEmRNAs were performed using the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. The miRNAs that are targeted by lncRNAs were predicted using miRanda and PITA, while the target mRNAs of miRNAs were retrieved from miRanda, miRWalk, and TargetScan. A protein-protein interaction (PPI) network was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) database, and then we constructed the lncRNA-miRNA-mRNA networks of ACC.\nRESULTS: Differentially expressed RNAs were identified in SACC. Upon comparing cancer tissues and NSG tissues, 103 upregulated and 52 downregulated lncRNAs and 745 upregulated and 866 downregulated mRNAs were identified in GSE88804; in addition, 39 upregulated and 43 downregulated miRNAs were identified in GSE117275. GO enrichment analyses revealed that the most relevant GO terms were regulation of transcription DNA-templated, transcription DNA-templated, and cell division. KEGG pathway enrichment analysis showed that differentially expressed genes (DEGs) were mainly enriched in the cell cycle, pathways in cancer, PI3K-Akt signaling pathway, breast cancer, and microRNAs in cancer. The PPI network consisted of 27 upregulated and 54 downregulated mRNAs. 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