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pmid:32571304

Construction and analysis of a lncRNA-miRNA-mRNA network based on competitive endogenous RNA reveal functional lncRNAs in oral cancer.

Junhao Yin · Xiaoli Zeng · Zexin Ai · Miao Yu · Yang'ou Wu · Shengjiao Li

BMC medical genomics · 2020 doi:10.1186/s12920-020-00741-w

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Experiment

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:32571304
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science-record
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2026-11-01T15:41:04Z
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paper object · 10 fields
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title
Construction and analysis of a lncRNA-miRNA-mRNA network based on competitive endogenous RNA reveal functional lncRNAs in oral cancer.
doi
10.1186/s12920-020-00741-w
pmid
32571304
authors array · 6 items
[0]
Junhao Yin
[1]
Xiaoli Zeng
[2]
Zexin Ai
[3]
Miao Yu
[4]
Yang'ou Wu
[5]
Shengjiao Li
journal
BMC medical genomics
year
2020
abstract
BACKGROUND: A growing evidence suggests that long non-coding RNAs (lncRNAs) can function as a microRNA (miRNA) sponge in various diseases including oral cancer. However, the pathophysiological function of lncRNAs remains unclear. METHODS: Based on the competitive endogenous RNA (ceRNA) theory, we constructed a lncRNA-miRNA-mRNA network in oral cancer with the human expression profiles GSE74530 from the Gene Expression Omnibus (GEO) database. We used topological analysis to determine the hub lncRNAs in the regulatory ceRNA network. Then, function enrichment analysis was performed using the clusterProfiler R package. Clinical information was downloaded from The Cancer Genome Atlas (TCGA) database and survival analysis was performed with Kaplan-Meier analysis. RESULTS: A total of 238 potential co-dysregulated competing triples were obtained in the lncRNA-associated ceRNA network in oral cancer, which consisted of 10 lncRNA nodes, 41 miRNA nodes and 122 mRNA nodes. Additionally, we found lncRNA HCG22 exhibiting superior potential as a diagnostic and prognostic marker of oral cancer. CONCLUSIONS: Our findings provide novel insights to understand the ceRNA regulation in oral cancer and identify a novel lncRNA as a potential molecular biomarker.
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Survival analysis was estimated based on Kaplan-Meier curve analysis.
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sections[21] "Survival analysis" paragraph 2
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Survival analysis was estimated based on Kaplan-Meier curve analysis.
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The datasets supporting the conclusions of this article were retrieved from the GEO repository (https://www.ncbi.nlm.nih.gov/geo/) with the accession number GSE74530 and the series matrix files were available at (ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE74nnn/GSE74530/matrix/). The raw data for data quality assessment was available at (https://www.ncbi.nlm.nih.gov/geo/download/?acc=GSE74530&format=file). The full data table of microarray platform GPL570 was available at (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GPL570). The human comprehensive gene annotation we used to identify lncRNAs was available at (ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_34/gencode.v34.annotation.gtf.gz). The case IDs and direct web links of all oral cancer samples obtained from the TCGA data portal (http://portal.gdc.cancer.gov/; dbGaP Study Accession: phs000178) by Bioconductor package TCGAbiolinks were shown in Additional file 2. Data banks/repositories corresponding to all datasets analyzed in this study were listed in Additional file 1.
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sections[30] "Availability of data and materials" paragraph 2
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The datasets supporting the conclusions of this article were retrieved from the GEO repository (https://www.ncbi.nlm.nih.gov/geo/) with the accession number GSE74530 and the series matrix files were available at (ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE74nnn/GSE74530/matrix/). The raw data for data quality assessment was available at (https://www.ncbi.nlm.nih.gov/geo/download/?acc=GSE74530&format=file). The full data table of microarray platform GPL570 was available at (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GPL570). The human comprehensive gene annotation we used to identify lncRNAs was available at (ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_34/gencode.v34.annotation.gtf.gz). The case IDs and direct web links of all oral cancer samples obtained from the TCGA data portal (http://portal.gdc.cancer.gov/; dbGaP Study Accession: phs000178) by Bioconductor package TCGAbiolinks were shown in Additional file 2. Data banks/repositories corresponding to all datasets analyzed in this study were listed in Additional file 1.
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Construction of the ceRNA network in oral cancer
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The effect characteristic of miRNAs in oral squamous cell carcinoma (OSCC)
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[2]
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[39]
[5] array · 4 items
[0]
hsa-miR-455-5p
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[40]
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[41]
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hsa-miR-140-5p
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[42]
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Topological analysis of the ceRNA network
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Table 2
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The list of differentially expressed genes (node degree > 5)
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[0]
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[1]
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[3]
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[1]
27
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hsa-miR-17-5p
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[1]
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[3]
lncRNA
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[1]
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[2]
hsa-miR-24-3p
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miRNA
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[1]
18
[2]
hsa-miR-27a-3p
[3]
miRNA
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[0]
6
[1]
17
[2]
hsa-miR-1297
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miRNA
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[1]
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[2]
hsa-miR-23b-3p
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miRNA
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[1]
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hsa-miR-140-5p
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miRNA
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[1]
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miRNA
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[0]
10
[1]
15
[2]
CRNDE
[3]
lncRNA
[11] array · 4 items
[0]
11
[1]
15
[2]
hsa-miR-22-3p
[3]
miRNA
[12] array · 4 items
[0]
12
[1]
15
[2]
hsa-miR-20b-5p
[3]
miRNA
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[0]
13
[1]
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lncRNA
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[1]
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lncRNA
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miRNA
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[1]
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miRNA
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[1]
13
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miRNA
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[1]
12
[2]
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lncRNA
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[1]
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miRNA
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[1]
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[3]
lncRNA
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[1]
11
[2]
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[3]
miRNA
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[1]
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miRNA
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[1]
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miRNA
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[1]
9
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miRNA
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[1]
9
[2]
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[1]
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YOD1
[3]
mRNA
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[1]
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lncRNA
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[1]
7
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[1]
7
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[1]
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[1]
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[1]
7
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[1]
7
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34
[1]
6
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mRNA
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[1]
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lncRNA
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6
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miRNA
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Topological analysis of the ceRNA network
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List of the 15 genes with the top betweenness centrality
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section[17]/table-wrap[2]#Tab3
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32571304", "kind": "science-record", "revision": 7, "content_hash": "sha256:eb5bf16ca9b573f8ebe39156c805cc2d151b3a503eaeee69b8a7c3dac5e492ff", "created_at": "2026-11-01T15:41:04Z", "updated_at": "2026-11-01T22:01:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction and analysis of a lncRNA-miRNA-mRNA network based on competitive endogenous RNA reveal functional lncRNAs in oral cancer.", "doi": "10.1186/s12920-020-00741-w", "pmid": "32571304", "authors": ["Junhao Yin", "Xiaoli Zeng", "Zexin Ai", "Miao Yu", "Yang'ou Wu", "Shengjiao Li"], "journal": "BMC medical genomics", "year": 2020, "abstract": "BACKGROUND: A growing evidence suggests that long non-coding RNAs (lncRNAs) can function as a microRNA (miRNA) sponge in various diseases including oral cancer. However, the pathophysiological function of lncRNAs remains unclear.\nMETHODS: Based on the competitive endogenous RNA (ceRNA) theory, we constructed a lncRNA-miRNA-mRNA network in oral cancer with the human expression profiles GSE74530 from the Gene Expression Omnibus (GEO) database. We used topological analysis to determine the hub lncRNAs in the regulatory ceRNA network. Then, function enrichment analysis was performed using the clusterProfiler R package. Clinical information was downloaded from The Cancer Genome Atlas (TCGA) database and survival analysis was performed with Kaplan-Meier analysis.\nRESULTS: A total of 238 potential co-dysregulated competing triples were obtained in the lncRNA-associated ceRNA network in oral cancer, which consisted of 10 lncRNA nodes, 41 miRNA nodes and 122 mRNA nodes. Additionally, we found lncRNA HCG22 exhibiting superior potential as a diagnostic and prognostic marker of oral cancer.\nCONCLUSIONS: Our findings provide novel insights to understand the ceRNA regulation in oral cancer and identify a novel lncRNA as a potential molecular biomarker.", "claims": [{"id": "claim-method", "statement": "Survival analysis was estimated based on Kaplan-Meier curve analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32571304", "locator": "sections[21] \"Survival analysis\" paragraph 2", "quote": "Survival analysis was estimated based on Kaplan-Meier curve analysis."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets supporting the conclusions of this article were retrieved from the GEO repository (https://www.ncbi.nlm.nih.gov/geo/) with the accession number GSE74530 and the series matrix files were available at (ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE74nnn/GSE74530/matrix/). 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The human comprehensive gene annotation we used to identify lncRNAs was available at (ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_34/gencode.v34.annotation.gtf.gz). The case IDs and direct web links of all oral cancer samples obtained from the TCGA data portal (http://portal.gdc.cancer.gov/; dbGaP Study Accession: phs000178) by Bioconductor package TCGAbiolinks were shown in Additional file 2. 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"blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["survival_km"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE74530"], "resolved_accessions": ["GSE74530"], "statements": ["The datasets supporting the conclusions of this article were retrieved from the GEO repository (https://www.ncbi.nlm.nih.gov/geo/) with the accession number GSE74530 and the series matrix files were available at (ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE74nnn/GSE74530/matrix/). The raw data for data quality assessment was available at (https://www.ncbi.nlm.nih.gov/geo/download/?acc=GSE74530&format=file). The full data table of microarray platform GPL570 was available at (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GPL570). The human comprehensive gene annotation we used to identify lncRNAs was available at (ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_34/gencode.v34.annotation.gtf.gz). The case IDs and direct web links of all oral cancer samples obtained from the TCGA data portal (http://portal.gdc.cancer.gov/; dbGaP Study Accession: phs000178) by Bioconductor package TCGAbiolinks were shown in Additional file 2. Data banks/repositories corresponding to all datasets analyzed in this study were listed in Additional file 1."], "basis": "The paper names GSE74530 in NCBI Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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