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pmid:34545330

Screening and Bioinformatics Analysis of Competitive Endogenous RNA Regulatory Network --Related to Circular RNA in Breast Cancer.

Tao Wang · Yi Zhang · Yan He · Yang Liu · Peng Qi

BioMed research international · 2021 doi:10.1155/2021/5575286

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

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:34545330
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science-record
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sha256:3992d6faef3cf2699a673f4fb53605e5300c0fdea0c0dbe578ede9ce65da0cf2
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2026-11-01T15:41:53Z
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2026-11-01T22:47:33Z
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title
Screening and Bioinformatics Analysis of Competitive Endogenous RNA Regulatory Network --Related to Circular RNA in Breast Cancer.
doi
10.1155/2021/5575286
pmid
34545330
authors array · 5 items
[0]
Tao Wang
[1]
Yi Zhang
[2]
Yan He
[3]
Yang Liu
[4]
Peng Qi
journal
BioMed research international
year
2021
abstract
PURPOSE: Circular RNA as a competitive endogenous RNA (ceRNA) plays a significant role in the pathogenesis and progression of breast cancer. In this study, a circular RNA-related ceRNA regulatory network was constructed, which provides new biomarkers and therapeutic targets for the treatment of breast cancer. Materials and methods. The expression profile datasets (GSE101123, GSE143564, GSE50428) of circRNAs, miRNAs, and mRNAs were downloaded from the GEO database, and then differentially expressed RNAs (DEcircRNAs, DEmiRNAs, DEmRNAs) were obtained through the CSCD, TargetScan, miRDB, and miRTarBase databases. CircRNA-miRNA pairs and miRNA-mRNA pairs were constructed. Finally, a ceRNA regulatory network was established. Downstream analysis of the ceRNA network included GO, KEGG analysis, survival analysis, sub-network construction, the BCIP, and qRT-PCR verification. RESULTS: In total, 144 differentially expressed (DE) DEcircRNA, 221 DEmiRNA, and 1211 DEmRNA were obtained, and 96 circRNA-miRNA pairs and 139 miRNA-mRNA pairs were constructed by prediction. The ceRNA regulatory network (circRNA-miRNA-mRNA) was constructed, which included 42 circRNA, 36miRNA, and 78 mRNA. GO function annotation showed genes were mainly enriched in receptor activity activated by transforming growth factor beta (TGF-beta) and in the regulation of epithelial cell apoptosis. KEGG analysis showed genes were mainly enriched in the TGF-beta signaling, PI3K-Akt signaling, and Wnt signaling pathways. Four genes associated with survival and prognosis of breast cancer were obtained by survival analysis, the prognostic sub-network included 4 circRNA, 4 miRNA, and 4 mRNA. BCIP analysis and qRT-PCR verification confirmed that relative mRNA expression levels were consistent with those in the GEO database. CONCLUSION: A circRNA-related ceRNA regulatory network was constructed for breast cancer in this study and key genes affecting pathogenesis and progression were identified. These findings may help better understand and further explore the molecular mechanisms that affect the progression and pathogenesis of breast cancer.
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sections[4] "2.2. Identification of DEcircRNA, DEmiRNA, DEmRNA Were Obtained" paragraph 2
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The three datasets (GSE101123, GSE143564, and GSE50428) in this study were downloaded from the GEO database (https://www.ncbi.nlm.nih.gov/gds/?term=).
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sections[21] "Data Availability" paragraph 2
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asset:data:geo:GSE101123 not downloaded
[2]
asset:data:geo:GSE143564 licence not read
[3]
asset:data:geo:GSE143564 not downloaded
[4]
asset:data:geo:GSE50428 licence not read
[5]
asset:data:geo:GSE50428 not downloaded
[6]
execution.not_run
[7]
review.human_critique
[8]
review.independent_reader
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review.machine_critique
assays array · 2 items
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apoptosis_assay
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99e1195c7d6f
confidence
0.69
evidence array · 1 item
[0]
ta) and in the regulation of epithelial cell apoptosis. KEGG analysis showed genes were mainly enri
order_basis
paper_text_order:1448
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assay:1
[1] object · 11 fields
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differential_expression
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source_hashes object · 1 field
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evidence array · 1 item
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DEcircRNA, DEmiRNA, and DEmRNA were obtained using the limma package in R version 4.0.3.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34545330", "kind": "science-record", "revision": 8, "content_hash": "sha256:3992d6faef3cf2699a673f4fb53605e5300c0fdea0c0dbe578ede9ce65da0cf2", "created_at": "2026-11-01T15:41:53Z", "updated_at": "2026-11-01T22:47:33Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Screening and Bioinformatics Analysis of Competitive Endogenous RNA Regulatory Network --Related to Circular RNA in Breast Cancer.", "doi": "10.1155/2021/5575286", "pmid": "34545330", "authors": ["Tao Wang", "Yi Zhang", "Yan He", "Yang Liu", "Peng Qi"], "journal": "BioMed research international", "year": 2021, "abstract": "PURPOSE: Circular RNA as a competitive endogenous RNA (ceRNA) plays a significant role in the pathogenesis and progression of breast cancer. In this study, a circular RNA-related ceRNA regulatory network was constructed, which provides new biomarkers and therapeutic targets for the treatment of breast cancer. Materials and methods. The expression profile datasets (GSE101123, GSE143564, GSE50428) of circRNAs, miRNAs, and mRNAs were downloaded from the GEO database, and then differentially expressed RNAs (DEcircRNAs, DEmiRNAs, DEmRNAs) were obtained through the CSCD, TargetScan, miRDB, and miRTarBase databases. CircRNA-miRNA pairs and miRNA-mRNA pairs were constructed. Finally, a ceRNA regulatory network was established. Downstream analysis of the ceRNA network included GO, KEGG analysis, survival analysis, sub-network construction, the BCIP, and qRT-PCR verification.\nRESULTS: In total, 144 differentially expressed (DE) DEcircRNA, 221 DEmiRNA, and 1211 DEmRNA were obtained, and 96 circRNA-miRNA pairs and 139 miRNA-mRNA pairs were constructed by prediction. The ceRNA regulatory network (circRNA-miRNA-mRNA) was constructed, which included 42 circRNA, 36miRNA, and 78 mRNA. GO function annotation showed genes were mainly enriched in receptor activity activated by transforming growth factor beta (TGF-beta) and in the regulation of epithelial cell apoptosis. KEGG analysis showed genes were mainly enriched in the TGF-beta signaling, PI3K-Akt signaling, and Wnt signaling pathways. Four genes associated with survival and prognosis of breast cancer were obtained by survival analysis, the prognostic sub-network included 4 circRNA, 4 miRNA, and 4 mRNA. BCIP analysis and qRT-PCR verification confirmed that relative mRNA expression levels were consistent with those in the GEO database.\nCONCLUSION: A circRNA-related ceRNA regulatory network was constructed for breast cancer in this study and key genes affecting pathogenesis and progression were identified. 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