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pmid:34539783

Identification of Differentially Expressed Circular RNAs as miRNA Sponges in Lung Adenocarcinoma.

Yuechao Liu · Xin Wang · Lulu Bi · Hongbo Huo · Shi Yan · Yimeng Cui · Yaowen Cui · Ruixue Gu · Dexin Jia · Shuai Zhang · Li Cai · Xiaomei Li · Ying Xing

Journal of oncology · 2021 doi:10.1155/2021/5193913

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:34539783
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science-record
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sha256:ceba0b86da74eaa9d84193a4546523e5e6522d288684fa64059ad5743b138948
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2026-11-01T15:41:53Z
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2026-11-01T21:26:16Z
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paper object · 10 fields
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title
Identification of Differentially Expressed Circular RNAs as miRNA Sponges in Lung Adenocarcinoma.
doi
10.1155/2021/5193913
pmid
34539783
authors array · 13 items
[0]
Yuechao Liu
[1]
Xin Wang
[2]
Lulu Bi
[3]
Hongbo Huo
[4]
Shi Yan
[5]
Yimeng Cui
[6]
Yaowen Cui
[7]
Ruixue Gu
[8]
Dexin Jia
[9]
Shuai Zhang
[10]
Li Cai
[11]
Xiaomei Li
[12]
Ying Xing
journal
Journal of oncology
year
2021
abstract
BACKGROUND: Circular RNAs (circRNAs) may function as the decoys for microRNAs (miRNAs) or proteins, the templates for translation, and the sources of pseudogene generation. The purpose of this study is to determine the diagnostic circRNAs, which are related to lung adenocarcinoma (LUAD), that adsorb miRNAs on the basis of the competing endogenous RNA (ceRNA) hypothesis. METHODS: The differentially expressed circRNAs (DEcircRNAs) in LUAD were revealed by the microarray data (GSE101586 and GSE101684) that were obtained from the Gene Expression Omnibus (GEO) database. The miRNAs that were targeted by the DEcircRNAs were predicted with the CircInteractome, and the target mRNAs of the miRNAs were found by the miRDB and the TargetScan. The ceRNA network was built by the Cytoscape. The potential biological roles and the regulatory mechanisms of the circRNAs were investigated by the Gene Ontology (GO) enrichment analysis and the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. The expression of the host genes of circRNAs was examined by the Ualcan. The survival analysis was performed by the Kaplan-Meier plotter. RESULTS: In comparison with normal lung tissues, LUAD tissues contained 7 overlapping cancer-specific DEcircRNAs with 294 miRNA response elements (MREs). Among the 7 DEcircRNAs, 3 circRNAs (hsa_circ_0072088, hsa_circ_0003528, and hsa_circ_0008274) were upregulated and 4 circRNAs (hsa_circ_0003162, hsa_circ_0029426, hsa_circ_0049271, and hsa_circ_0043256) were downregulated. A circRNA-miRNA-mRNA regulatory network, which included 33 differentially expressed miRNAs (DEmiRNAs) and 2007 differentially expressed mRNAs (DEmRNAs), was constructed. These mRNAs were enriched in the biological function of cell-cell adhesion, response to hypoxia, and stem cell differentiation and were involved in the PI3K-Akt signaling, HIF-1 signaling, and cAMP signaling pathways. CONCLUSION: Our results indicated that 7 DEcircRNAs could have diagnostic value for LUAD. Additionally, the circRNAs-mediated ceRNA network might provide a novel perspective into unraveling the pathogenesis and progression of LUAD.
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The differences were compared by paired t-test.
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All data generated or analyzed during this study are included in this published article and its supplementary information files.
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Profiling circular RNA expression in lung cancer
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MiRNA microarray analysis of 5 fresh lung cancer tissues and 5 fresh non-tumor lung tissues
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3.2. Characterization of DEcircRNAs
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As (DEcircRNAs) in LUAD were revealed by the microarray data (GSE101586 and GSE101684) that were obt
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34539783", "kind": "science-record", "revision": 6, "content_hash": "sha256:ceba0b86da74eaa9d84193a4546523e5e6522d288684fa64059ad5743b138948", "created_at": "2026-11-01T15:41:53Z", "updated_at": "2026-11-01T21:26:16Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of Differentially Expressed Circular RNAs as miRNA Sponges in Lung Adenocarcinoma.", "doi": "10.1155/2021/5193913", "pmid": "34539783", "authors": ["Yuechao Liu", "Xin Wang", "Lulu Bi", "Hongbo Huo", "Shi Yan", "Yimeng Cui", "Yaowen Cui", "Ruixue Gu", "Dexin Jia", "Shuai Zhang", "Li Cai", "Xiaomei Li", "Ying Xing"], "journal": "Journal of oncology", "year": 2021, "abstract": "BACKGROUND: Circular RNAs (circRNAs) may function as the decoys for microRNAs (miRNAs) or proteins, the templates for translation, and the sources of pseudogene generation. The purpose of this study is to determine the diagnostic circRNAs, which are related to lung adenocarcinoma (LUAD), that adsorb miRNAs on the basis of the competing endogenous RNA (ceRNA) hypothesis.\nMETHODS: The differentially expressed circRNAs (DEcircRNAs) in LUAD were revealed by the microarray data (GSE101586 and GSE101684) that were obtained from the Gene Expression Omnibus (GEO) database. The miRNAs that were targeted by the DEcircRNAs were predicted with the CircInteractome, and the target mRNAs of the miRNAs were found by the miRDB and the TargetScan. The ceRNA network was built by the Cytoscape. The potential biological roles and the regulatory mechanisms of the circRNAs were investigated by the Gene Ontology (GO) enrichment analysis and the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. The expression of the host genes of circRNAs was examined by the Ualcan. The survival analysis was performed by the Kaplan-Meier plotter.\nRESULTS: In comparison with normal lung tissues, LUAD tissues contained 7 overlapping cancer-specific DEcircRNAs with 294 miRNA response elements (MREs). Among the 7 DEcircRNAs, 3 circRNAs (hsa_circ_0072088, hsa_circ_0003528, and hsa_circ_0008274) were upregulated and 4 circRNAs (hsa_circ_0003162, hsa_circ_0029426, hsa_circ_0049271, and hsa_circ_0043256) were downregulated. A circRNA-miRNA-mRNA regulatory network, which included 33 differentially expressed miRNAs (DEmiRNAs) and 2007 differentially expressed mRNAs (DEmRNAs), was constructed. These mRNAs were enriched in the biological function of cell-cell adhesion, response to hypoxia, and stem cell differentiation and were involved in the PI3K-Akt signaling, HIF-1 signaling, and cAMP signaling pathways.\nCONCLUSION: Our results indicated that 7 DEcircRNAs could have diagnostic value for LUAD. 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