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pmid:34485109

Screening and Identification of Key Biomarkers of Gastric Cancer: Three Genes Jointly Predict Gastric Cancer.

Meng-Jie Shan · Ling-Bing Meng · Peng Guo · Yuan-Meng Zhang · Dexian Kong · Ya-Bin Liu

Frontiers in oncology · 2021 doi:10.3389/fonc.2021.591893

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:34485109
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2026-11-01T15:41:50Z
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paper object · 10 fields
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title
Screening and Identification of Key Biomarkers of Gastric Cancer: Three Genes Jointly Predict Gastric Cancer.
doi
10.3389/fonc.2021.591893
pmid
34485109
authors array · 6 items
[0]
Meng-Jie Shan
[1]
Ling-Bing Meng
[2]
Peng Guo
[3]
Yuan-Meng Zhang
[4]
Dexian Kong
[5]
Ya-Bin Liu
journal
Frontiers in oncology
year
2021
abstract
BACKGROUND: Gastric cancer (GC) is one of the most common cancers all over the world, causing high mortality. Gastric cancer screening is one of the effective strategies used to reduce mortality. We expect that good biomarkers can be discovered to diagnose and treat gastric cancer as early as possible. METHODS: We download four gene expression profiling datasets of gastric cancer (GSE118916, GSE54129, GSE103236, GSE112369), which were obtained from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) between gastric cancer and adjacent normal tissues were detected to explore biomarkers that may play an important role in gastric cancer. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of overlap genes were conducted by the Metascape online database; the protein-protein interaction (PPI) network was constructed by the STRING online database, and we screened the hub genes of the PPI network using the Cytoscape software. The survival curve analysis was conducted by km-plotter and the stage plots of hub genes were created by the GEPIA online database. PCR, WB, and immunohistochemistry were used to verify the expression of hub genes. A neural network model was established to quantify the predictors of gastric cancer. RESULTS: The relative expression level of cadherin-3 (CDH3), lymphoid enhancer-binding factor 1 (LEF1), and matrix metallopeptidase 7 (MMP7) were significantly higher in gastric samples, compared with the normal groups (p<0.05). Receiver operator characteristic (ROC) curves were constructed to determine the effect of the three genes' expression on gastric cancer, and the AUC was used to determine the degree of confidence: CDH3 (AUC = 0.800, P<0.05, 95% CI =0.857-0.895), LEF1 (AUC=0.620, P<0.05, 95%CI=0.632-0.714), and MMP7 (AUC=0.914, P<0.05, 95%CI=0.714-0.947). The high-risk warning indicator of gastric cancer contained 8<CDH3<15 and 10<expression of LEF1<16. CONCLUSIONS: CDH3, LEF1, and MMP7 can be used as candidate biomarkers to construct a neural network model from hub genes, which may be helpful for the early diagnosis of gastric cancer.
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sections[29] "Data Availability Statement" paragraph 2
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
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Expression data from human gastric tumor and human normal stomach tissues
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Global gene expression analysis of gastric cancer by oligonucleotide microarrays
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Functional enrichment analysis of DEGs in gastric cancer using GSEA.
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Functional enrichment analysis of DEGs in gastric cancer using GSEA.
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Pathway enrichment analysis of DEGs in gastric cancer using GSEA.
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Functional Annotation
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Pathway enrichment analysis of DEGs in gastric cancer using GSEA.
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The correlation and linear regression analysis between GC and relevant gene expression.
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Association Between Three Genes and Gastric Cancer by Pearson’s Correlation Test and Univariate Linear Regression
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The correlation and linear regression analysis between GC and relevant gene expression.
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[3]
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section[23]/table-wrap[1]#T4
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f genes. Animal Models Ten BALB/c-nu-nu nude mice were used to construct a gastric cancer mouse mod
[1]
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y Figure 1(A) Relative expression of MMP7 in mouse model of carcinoma in situ by RT-qPCR analysis. P<
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control. (B) Relative expression of CDH3 in mouse model of carcinoma in situ by RT-qPCR analysis. P<
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34485109", "kind": "science-record", "revision": 7, "content_hash": "sha256:cc456a6f11c4d9065f36b6a2e96755051dd9e3f31563bf7be2d0c4d4f42491dd", "created_at": "2026-11-01T15:41:50Z", "updated_at": "2026-11-01T22:04:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Screening and Identification of Key Biomarkers of Gastric Cancer: Three Genes Jointly Predict Gastric Cancer.", "doi": "10.3389/fonc.2021.591893", "pmid": "34485109", "authors": ["Meng-Jie Shan", "Ling-Bing Meng", "Peng Guo", "Yuan-Meng Zhang", "Dexian Kong", "Ya-Bin Liu"], "journal": "Frontiers in oncology", "year": 2021, "abstract": "BACKGROUND: Gastric cancer (GC) is one of the most common cancers all over the world, causing high mortality. Gastric cancer screening is one of the effective strategies used to reduce mortality. We expect that good biomarkers can be discovered to diagnose and treat gastric cancer as early as possible.\nMETHODS: We download four gene expression profiling datasets of gastric cancer (GSE118916, GSE54129, GSE103236, GSE112369), which were obtained from the Gene Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) between gastric cancer and adjacent normal tissues were detected to explore biomarkers that may play an important role in gastric cancer. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of overlap genes were conducted by the Metascape online database; the protein-protein interaction (PPI) network was constructed by the STRING online database, and we screened the hub genes of the PPI network using the Cytoscape software. The survival curve analysis was conducted by km-plotter and the stage plots of hub genes were created by the GEPIA online database. PCR, WB, and immunohistochemistry were used to verify the expression of hub genes. A neural network model was established to quantify the predictors of gastric cancer.\nRESULTS: The relative expression level of cadherin-3 (CDH3), lymphoid enhancer-binding factor 1 (LEF1), and matrix metallopeptidase 7 (MMP7) were significantly higher in gastric samples, compared with the normal groups (p<0.05). Receiver operator characteristic (ROC) curves were constructed to determine the effect of the three genes' expression on gastric cancer, and the AUC was used to determine the degree of confidence: CDH3 (AUC = 0.800, P<0.05, 95% CI =0.857-0.895), LEF1 (AUC=0.620, P<0.05, 95%CI=0.632-0.714), and MMP7 (AUC=0.914, P<0.05, 95%CI=0.714-0.947). The high-risk warning indicator of gastric cancer contained 8<CDH3<15 and 10<expression of LEF1<16.\nCONCLUSIONS: CDH3, LEF1, and MMP7 can be used as candidate biomarkers to construct a neural network model from hub genes, which may be helpful for the early diagnosis of gastric cancer.", "claims": [{"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34485109", "locator": "sections[29] \"Data Availability Statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. 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