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pmid:32821169

Construction and Comprehensive Analysis of a ceRNA Network to Reveal Potential Novel Biomarkers for Triple-Negative Breast Cancer.

Lifei Ma · Guiqin Song · Meiyu Li · Xiuqing Hao · Yong Huang · Jinping Lan · Siqian Yang · Zetian Zhang · Guohui Zhang · Jiao Mu

Cancer management and research · 2020 doi:10.2147/CMAR.S260150

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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title
Construction and Comprehensive Analysis of a ceRNA Network to Reveal Potential Novel Biomarkers for Triple-Negative Breast Cancer.
doi
10.2147/CMAR.S260150
pmid
32821169
authors array · 10 items
[0]
Lifei Ma
[1]
Guiqin Song
[2]
Meiyu Li
[3]
Xiuqing Hao
[4]
Yong Huang
[5]
Jinping Lan
[6]
Siqian Yang
[7]
Zetian Zhang
[8]
Guohui Zhang
[9]
Jiao Mu
journal
Cancer management and research
year
2020
abstract
BACKGROUND: Triple-negative breast cancer (TNBC) is the most common and aggressive type of breast cancer with an unfavourable outcome worldwide. Novel therapeutic targets are urgently required to explore this malignancy. This study explored the ceRNA network and the important genes for predicting the therapeutic targets. METHODS: It identified the differentially expressed genes of mRNAs, lncRNAs and miRNAs between TNBC and non-TNBC samples in four cohorts (TCGA, GSE38959, GSE45827 and GSE65194) to explore the novel therapeutic targets for TNBC. Downstream analyses, including functional enrichment analysis, ceRNA network, protein-protein interaction and survival analysis, were then conducted by bioinformatics analysis. Finally, the potential core protein of the ceRNA network in TNBC was validated by immunohistochemistry. RESULTS: A total of 1,045 lncRNAs and 28 miRNAs were differentially expressed in the TCGA TNBC samples, and the intersections of 282 mRNAs (176 upregulations and 106 downregulations) between the GEO and TCGA databases were identified. A ceRNA network composed of 7 lncRNAs, 62 mRNAs, 12 miRNAs and 244 edges specific to TNBC was established. The functional assay showed dysregulated genes, and GO, DO and KEGG enrichment analysis were performed. Survival analysis showed that mRNA LIFR and lncRNA AC124312.3 were significantly correlated with the overall survival of patients with TNBC in the TCGA databases (P < 0.05). Finally, the LIFR protein was validated, and immunohistochemical results showed the upregulated expression of LIFR in TNBC tissues. CONCLUSION: Thus, our study presents an enhanced understanding of the ceRNA network in TNBC, where the key gene LIFR may be a new promising potential therapeutic target for patients with TNBC.
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To further explore the role of genes in the ceRNA network, the Overall Survival (OS) Kaplan–Meier Estimate was applied for survival analysis by using the survival R package. The datasets involved in this study were composed of TCGA breast cancer samples and filtered using the negative expressions of ER, PR and HER-2 according to their clinical information. For each gene, the cancerous samples were divided into two subgroups according to the optimal cut-off value (50%) of the gene expression, and the Logrank Test P value of less than 0.05 was presented.
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To further explore the role of genes in the ceRNA network, the Overall Survival (OS) Kaplan–Meier Estimate was applied for survival analysis by using the survival R package.
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The datasets involved in this study were composed of TCGA breast cancer samples and filtered using the negative expressions of ER, PR and HER-2 according to their clinical information.
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sections[8] "Survival Analysis of ceRNA Network" paragraph 2
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For each gene, the cancerous samples were divided into two subgroups according to the optimal cut-off value (50%) of the gene expression, and the Logrank Test P value of less than 0.05 was presented.
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quote
To further explore the role of genes in the ceRNA network, the Overall Survival (OS) Kaplan–Meier Estimate was applied for survival analysis by using the survival R package. The datasets involved in this study were composed of TCGA breast cancer samples and filtered using the negative expressions of ER, PR and HER-2 according to their clinical information. For each gene, the cancerous samples were divided into two subgroups according to the optimal cut-off value (50%) of the gene expression, and the Logrank Test P value of less than 0.05 was presented.
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Principal component analysis
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protein-protein interaction
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Automated Assays Laravel application and simulated adapters
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: log_rank_test.
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GSE38959
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The data analyzed in this study can be downloaded from the TCGA and GEO.
basis
The paper names GSE38959, GSE45827, GSE65194 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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f the ceRNA network in TNBC was validated by immunohistochemistry. RESULTS: A total of 1,045 lncRNAs and 28 mi
[1]
Finally, the LIFR protein was validated, and immunohistochemical results showed the upregulated expression of
[2]
amination by haematoxylin-eosin staining and immunohistochemistry from the First Affiliated Hospital of Hebei
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ta (lncRNA and mRNA, level 3; Illumina HiSeq RNA-Seq platform) and miRNA sequence data (Illumina
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d Methods Data Retrieval and Patient Samples RNA sequencing data and clinical information with human TNB
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To further explore the role of genes in the ceRNA network, the Overall Survival (OS) Kaplan–Meier Estimate was applied for survival analysis by using the survival R package. The datasets involved in this study were composed of TCGA breast cancer samples and filtered using the negative expressions of ER, PR and HER-2 according to their clinical information. For each gene, the cancerous samples were divided into two subgroups according to the optimal cut-off value (50%) of the gene expression, and the Logrank Test P value of less than 0.05 was presented.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32821169", "kind": "science-record", "revision": 7, "content_hash": "sha256:995565c4b8802f16aa8261df9b1ff2e764abca2fc028ed8dde3ebb750c6cec2b", "created_at": "2026-11-01T15:41:08Z", "updated_at": "2026-11-01T22:02:03Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction and Comprehensive Analysis of a ceRNA Network to Reveal Potential Novel Biomarkers for Triple-Negative Breast Cancer.", "doi": "10.2147/CMAR.S260150", "pmid": "32821169", "authors": ["Lifei Ma", "Guiqin Song", "Meiyu Li", "Xiuqing Hao", "Yong Huang", "Jinping Lan", "Siqian Yang", "Zetian Zhang", "Guohui Zhang", "Jiao Mu"], "journal": "Cancer management and research", "year": 2020, "abstract": "BACKGROUND: Triple-negative breast cancer (TNBC) is the most common and aggressive type of breast cancer with an unfavourable outcome worldwide. Novel therapeutic targets are urgently required to explore this malignancy. This study explored the ceRNA network and the important genes for predicting the therapeutic targets.\nMETHODS: It identified the differentially expressed genes of mRNAs, lncRNAs and miRNAs between TNBC and non-TNBC samples in four cohorts (TCGA, GSE38959, GSE45827 and GSE65194) to explore the novel therapeutic targets for TNBC. Downstream analyses, including functional enrichment analysis, ceRNA network, protein-protein interaction and survival analysis, were then conducted by bioinformatics analysis. Finally, the potential core protein of the ceRNA network in TNBC was validated by immunohistochemistry.\nRESULTS: A total of 1,045 lncRNAs and 28 miRNAs were differentially expressed in the TCGA TNBC samples, and the intersections of 282 mRNAs (176 upregulations and 106 downregulations) between the GEO and TCGA databases were identified. A ceRNA network composed of 7 lncRNAs, 62 mRNAs, 12 miRNAs and 244 edges specific to TNBC was established. The functional assay showed dysregulated genes, and GO, DO and KEGG enrichment analysis were performed. Survival analysis showed that mRNA LIFR and lncRNA AC124312.3 were significantly correlated with the overall survival of patients with TNBC in the TCGA databases (P < 0.05). Finally, the LIFR protein was validated, and immunohistochemical results showed the upregulated expression of LIFR in TNBC tissues.\nCONCLUSION: Thus, our study presents an enhanced understanding of the ceRNA network in TNBC, where the key gene LIFR may be a new promising potential therapeutic target for patients with TNBC.", "claims": [{"id": "claim-method", "statement": "To further explore the role of genes in the ceRNA network, the Overall Survival (OS) Kaplan–Meier Estimate was applied for survival analysis by using the survival R package. The datasets involved in this study were composed of TCGA breast cancer samples and filtered using the negative expressions of ER, PR and HER-2 according to their clinical information. 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