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pmid:33532293

Identification of a potentially functional circRNA-miRNA-mRNA ceRNA regulatory network in bladder cancer by analysis of microarray data.

Lei Du · Xin Wang · Yuewei Yin · Yanping Zhang · Jianghua Jia · Baosai Lu · Wenyong Xue · Changbao Qu · Jinchun Qi

Translational andrology and urology · 2021 doi:10.21037/tau-20-660

Paper

complete

Experiment

complete

Data

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Analysis

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Identification of a potentially functional circRNA-miRNA-mRNA ceRNA regulatory network in bladder cancer by analysis of microarray data.
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10.21037/tau-20-660
pmid
33532293
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[0]
Lei Du
[1]
Xin Wang
[2]
Yuewei Yin
[3]
Yanping Zhang
[4]
Jianghua Jia
[5]
Baosai Lu
[6]
Wenyong Xue
[7]
Changbao Qu
[8]
Jinchun Qi
journal
Translational andrology and urology
year
2021
abstract
BACKGROUND: Circular RNAs (circRNAs) have received increasing attention in cancer development. However, a substantial number of circRNAs still require characterization. The purpose of this study is to uncover novel circRNAs and their molecular mechanism in bladder cancer (BCa). METHODS: A combinative strategy of extensive data mining and computational biology was employed to identify BCa-related circRNAs and explore their potential mechanisms of action. RESULTS: Three differentially expressed circRNAs (has_circ_0023642, has_circ_0047322, has_circ_0041151) were obtained from the microarray dataset (GSE92675). Four miRNAs (miR-616, miR-515-5p, miR-647, miR-1178) with potential binding sites with these three circRNAs were identified. Pathway analysis demonstrated that all four miRNAs were closely associated with some cancer-related pathways. Survival analysis indicated that these miRNAs might potentially play a role in tumor-suppressive functions in BCa. Subsequently, 181 overlapping genes were identified from 472 up-regulated genes in BCa (TCGA database), and 10,017 predicted target genes of the four miRNAs obtained. A circRNA-miRNA-mRNA network was constructed on the identified three circRNAs, four miRNAs, and 181 overlapping genes. Besides, six hub genes (CENPA, HIST1H2BJ, HIST1H2BO, HIST1H3H, HIST1H3B, HIST1H3F) were identified from establishing a protein-protein interaction (PPI) network on the same overlapping genes. Furthermore, a circRNA-miRNA-hub gene sub-network was built to delineate the links among the differential circRNAs, miRNA, and hub genes. CONCLUSIONS: Our study provided significant insights into the molecular mechanisms that regulate the progression of BCa from the circRNA-miRNA-mRNA network view.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33532293", "kind": "science-record", "revision": 8, "content_hash": "sha256:112af00db6f169ecf85fb93fc283d49cb02a39d6c8197bbc551afdc6f1dc083e", "created_at": "2026-11-01T15:41:24Z", "updated_at": "2026-11-01T22:03:02Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of a potentially functional circRNA-miRNA-mRNA ceRNA regulatory network in bladder cancer by analysis of microarray data.", "doi": "10.21037/tau-20-660", "pmid": "33532293", "authors": ["Lei Du", "Xin Wang", "Yuewei Yin", "Yanping Zhang", "Jianghua Jia", "Baosai Lu", "Wenyong Xue", "Changbao Qu", "Jinchun Qi"], "journal": "Translational andrology and urology", "year": 2021, "abstract": "BACKGROUND: Circular RNAs (circRNAs) have received increasing attention in cancer development. However, a substantial number of circRNAs still require characterization. The purpose of this study is to uncover novel circRNAs and their molecular mechanism in bladder cancer (BCa).\nMETHODS: A combinative strategy of extensive data mining and computational biology was employed to identify BCa-related circRNAs and explore their potential mechanisms of action.\nRESULTS: Three differentially expressed circRNAs (has_circ_0023642, has_circ_0047322, has_circ_0041151) were obtained from the microarray dataset (GSE92675). Four miRNAs (miR-616, miR-515-5p, miR-647, miR-1178) with potential binding sites with these three circRNAs were identified. Pathway analysis demonstrated that all four miRNAs were closely associated with some cancer-related pathways. Survival analysis indicated that these miRNAs might potentially play a role in tumor-suppressive functions in BCa. Subsequently, 181 overlapping genes were identified from 472 up-regulated genes in BCa (TCGA database), and 10,017 predicted target genes of the four miRNAs obtained. A circRNA-miRNA-mRNA network was constructed on the identified three circRNAs, four miRNAs, and 181 overlapping genes. Besides, six hub genes (CENPA, HIST1H2BJ, HIST1H2BO, HIST1H3H, HIST1H3B, HIST1H3F) were identified from establishing a protein-protein interaction (PPI) network on the same overlapping genes. Furthermore, a circRNA-miRNA-hub gene sub-network was built to delineate the links among the differential circRNAs, miRNA, and hub genes.\nCONCLUSIONS: Our study provided significant insights into the molecular mechanisms that regulate the progression of BCa from the circRNA-miRNA-mRNA network view.", "claims": [{"id": "claim-method", "statement": "The correlation between miRNA expression and patients’ survival was assessed by Kaplan-Meier method.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33532293", "locator": "sections[10] \"Statistical analysis\" paragraph 2", "quote": "The correlation between miRNA expression and patients’ survival was assessed by Kaplan-Meier method."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The circRNA expression profile of GSE92675 was obtained from the GEO database, including 4 pairs of matched BCa (GSM2434319, GSM2434321, GSM2434323, GSM2434325) and para-cancer tissues (GSM2434320, GSM2434322, GSM2434324, GSM2434326).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33532293", "locator": "sections[3] \"Data collection\" paragraph 2", "quote": "The circRNA expression profile of GSE92675 was obtained from the GEO database, including 4 pairs of matched BCa (GSM2434319, GSM2434321, GSM2434323, GSM2434325) and para-cancer tissues (GSM2434320, GSM2434322, GSM2434324, GSM2434326)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:33532293"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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