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pmid:28490889

Identification of potential biomarkers and analysis of prognostic values in head and neck squamous cell carcinoma by bioinformatics analysis.

Bo Yang · Zhifeng Chen · Yu Huang · Guoxu Han · Weizhong Li

OncoTargets and therapy · 2017 doi:10.2147/OTT.S135514

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Experiment

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Data

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Analysis

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pmid:28490889
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2026-11-01T15:40:25Z
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title
Identification of potential biomarkers and analysis of prognostic values in head and neck squamous cell carcinoma by bioinformatics analysis.
doi
10.2147/OTT.S135514
pmid
28490889
authors array · 5 items
[0]
Bo Yang
[1]
Zhifeng Chen
[2]
Yu Huang
[3]
Guoxu Han
[4]
Weizhong Li
journal
OncoTargets and therapy
year
2017
abstract
The purpose of this study was to find disease-associated genes and potential mechanisms in head and neck squamous cell carcinoma (HNSCC) with deoxyribonucleic acid microarrays. The gene expression profiles of GSE6791 were downloaded from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were obtained with packages in R language and STRING constructed protein-protein interaction (PPI) network of the DEGs with combined score >0.8. Subsequently, module analysis of the PPI network was performed by Molecular Complex Detection plugin and functions and pathways of the hub gene in subnetwork were studied. Finally, overall survival analysis of hub genes was verified in TCGA HNSCC cohort. A total of 811 DEGs were obtained, which were mainly enriched in the terms related to extracellular matrix (ECM)-receptor interaction, ECM structural constituent, and ECM organization. A PPI network was constructed, consisting of 401 nodes and 1,254 edges and 15 hub genes with high degrees in the network. High expression of 4 genes of the 15 genes was associated with poor OS of patients in HNSCC, including PSMA7, ITGA6, ITGB4, and APP. Two significant modules were detected from the PPI network, and the enriched functions and pathways included proteasome, ECM organization, and ECM-receptor interaction. In conclusion, we propose that PSMA7, ITGA6, ITGB4, and APP may be further explored as potential biomarkers to aid HNSCC diagnosis and treatment.
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Then, the DEGs between HNSCC samples and normal controls were identified using the empirical Bayes approach in linear models for the microarray data (limma) package.
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sections[4] "Data preprocessing and identification of DEGs" paragraph 2
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Then, the DEGs between HNSCC samples and normal controls were identified using the empirical Bayes approach in linear models for the microarray data (limma) package.
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Microarray expression profiles of GSE67917 were downloaded from Gene Expression Omnibus database for identifying DEGs of HNSCC. GSE6791, which was already deposited in GPL570 (Affymetrix Human Genome U133 Plus 2.0 Array, Santa Clara, CA, USA), consisted of 42 HNSCC samples and 14 normal epithelial samples.
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sections[3] "Microarray data" paragraph 2
quote
Microarray expression profiles of GSE67917 were downloaded from Gene Expression Omnibus database for identifying DEGs of HNSCC. GSE6791, which was already deposited in GPL570 (Affymetrix Human Genome U133 Plus 2.0 Array, Santa Clara, CA, USA), consisted of 42 HNSCC samples and 14 normal epithelial samples.
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Using limma on the GSE6791 microarray dataset, the study identified 811 differentially expressed genes between 42 HNSCC samples and 14 normal epithelial samples, including 550 upregulated and 261 downregulated genes.
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sections[4] "Data preprocessing and identification of DEGs" paragraph 2
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Then, the DEGs between HNSCC samples and normal controls were identified using the empirical Bayes approach in linear models for the microarray data (limma) package.
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sections[9] "Identification of DEGs" paragraph 2
quote
The total number of samples analyzed was 42 HNSCC samples, along with 14 normal epithelial samples. After data preprocessing, DEG analysis was performed using the limma software package. A total of 811 genes were identified after the analyses of GSE6791, including 550 upregulated and 261 downregulated genes.
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Using limma on the GSE6791 microarray dataset, the study identified 811 differentially expressed genes between 42 HNSCC samples and 14 normal epithelial samples, including 550 upregulated and 261 downregulated genes.
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Microarray expression profiles of GSE67917 were downloaded from Gene Expression Omnibus database for identifying DEGs of HNSCC. GSE6791, which was already deposited in GPL570 (Affymetrix Human Genome U133 Plus 2.0 Array, Santa Clara, CA, USA), consisted of 42 HNSCC samples and 14 normal epithelial samples.
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Functional and pathway enrichment analysis of upregulated and downregulated DEGs in HNSCC
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2.07E–18
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The hub genes that had a degree >22 in PPI network
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Coexpression network analysis of DEGs
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The hub genes that had a degree >22 in PPI network
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Functional and pathway enrichment analysis of the DEGs in modules
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[3]
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[3]
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[1]
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[3]
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[1]
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[3]
2.90E–17
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[3]
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[14] array · 4 items
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[3]
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[1]
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[1]
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[3]
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[3]
7.43E–17
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[0]
Hsa:04151
[1]
PI3K-Akt signaling pathway
[2]
15
[3]
2.72E–16
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[0]
Hsa:05222
[1]
Small cell lung cancer
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7
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3.22E–08
locator
section[11]/table-wrap[2]#t3-ott-10-2315
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[0]
asset:data:geo:GSE6791 not downloaded
[1]
asset:data:geo:GSE6791 licence not read
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differential_expression
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Differential expression analysis
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Then, the DEGs between HNSCC samples and normal controls were identified using the empirical Bayes approach in linear models for the microarray data (limma) package.
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[2] object · 10 fields
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network_analysis
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[2]
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Network / pathway analysis
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pathway enrichment
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capability:computational_analysis
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[1]
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[6]
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[7]
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[8]
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candidate
Automated Assays Laravel application and simulated adapters
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
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[0]
GSE6791
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[0]
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[0]
Microarray expression profiles of GSE67917 were downloaded from Gene Expression Omnibus database for identifying DEGs of HNSCC. GSE6791, which was already deposited in GPL570 (Affymetrix Human Genome U133 Plus 2.0 Array, Santa Clara, CA, USA), consisted of 42 HNSCC samples and 14 normal epithelial samples.
basis
The paper names GSE6791 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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Then, the DEGs between HNSCC samples and normal controls were identified using the empirical Bayes approach in linear models for the microarray data (limma) package.
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The gene expression profiles of GSE6791 were downloaded from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were obtained with packages in R language and STRING constructed protein-protein interaction (PPI) network of the DEGs with combined score >0.8. Subsequently, module analysis of the PPI network was performed by Molecular Complex Detection plugin and functions and pathways of the hub gene in subnetwork were studied. Finally, overall survival analysis of hub genes was verified in TCGA HNSCC cohort. A total of 811 DEGs were obtained, which were mainly enriched in the terms related to extracellular matrix (ECM)-receptor interaction, ECM structural constituent, and ECM organization. A PPI network was constructed, consisting of 401 nodes and 1,254 edges and 15 hub genes with high degrees in the network. High expression of 4 genes of the 15 genes was associated with poor OS of patients in HNSCC, including PSMA7, ITGA6, ITGB4, and APP. Two significant modules were detected from the PPI network, and the enriched functions and pathways included proteasome, ECM organization, and ECM-receptor interaction. 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{"label": "Table 3", "caption": "Functional and pathway enrichment analysis of the DEGs in modules", "rows": [["ID", "Description", "Count", "P-value"], ["Module 1", "", "", ""], ["GO_BP:0031145", "Anaphase-promoting complex-dependent catabolic process", "17", "1.73E–36"], ["GO_BP:0051436", "Negative regulation of ubiquitin protein ligase activity involved in mitotic cell cycle", "16", "4.09E–34"], ["GO_BP:0051437", "Positive regulation of ubiquitin protein ligase activity involved in regulation of mitotic cell cycle transition", "16", "1.27E–33"], ["GO_BP:0006521", "Regulation of cellular amino acid metabolic process", "14", "2.99E–30"], ["GO_BP:0043161", "Proteasome-mediated ubiquitin-dependent protein catabolic process", "16", "8.04E–27"], ["GO_CC:0000502", "Proteasome complex", "12", "5.82E–24"], ["GO_CC:0005839", "Proteasome core complex", "8", "2.77E–17"], ["GO_CC:0005829", "Cytosol", "19", "4.58E–14"], ["GO_CC:0005654", "Nucleoplasm", "16", "2.87E–10"], ["GO_CC:0005634", "Nucleus", "18", "1.40E–08"], ["GO_MF:0004298", "Threonine-type endopeptidase activity", "8", "2.90E–17"], ["GO_MF:0005515", "Protein binding", "18", "1.49E–05"], ["Hsa:03050", "Proteasome", "12", "2.16E–21"], ["Module 2", "", "", ""], ["GO_BP:0030198", "ECM organization", "17", "5.98E–29"], ["GO_BP:0030574", "Collagen catabolic process", "12", "7.33E–23"], ["GO_BP:0030199", "Collagen fibril organization", "7", "2.78E–12"], ["GO_BP:0071230", "Cellular response to amino acid stimulus", "7", "9.11E–12"], ["GO_BP:0007155", "Cell adhesion", "9", "1.70E–08"], ["GO_CC:0005788", "Endoplasmic reticulum lumen", "15", "1.42E–24"], ["GO_CC:0005581", "Collagen trimer", "11", "5.76E–19"], ["GO_CC:0005576", "Extracellular region", "15", "1.27E–11"], ["GO_CC:0031012", "ECM", "9", "2.85E–10"], ["GO_CC:0005578", "Proteinaceous ECM", "8", "5.96E–09"], ["GO_MF:0005201", "ECM structural constituent", "11", "4.30E–20"], ["GO_MF:0048407", "Platelet-derived growth factor binding", "5", "3.76E–10"], ["GO_MF:0038132", "Neuregulin binding", "3", "1.20E–05"], ["Hsa:04512", "ECM–receptor interaction", "15", "5.56E–25"], ["Hsa:04974", "Protein digestion and absorption", "13", "4.91E–20"], ["Hsa:04510", "Focal adhesion", "15", "1.76E–19"], ["Hsa:05146", "Amebiasis", "12", "7.43E–17"], ["Hsa:04151", "PI3K-Akt signaling pathway", "15", "2.72E–16"], ["Hsa:05222", "Small cell lung cancer", "7", "3.22E–08"]], "row_count": 35, "column_count": 4, "numeric_cells": 98, "header_rows": 1, "locator": "section[11]/table-wrap[2]#t3-ott-10-2315"}}], "gaps": ["asset:data:geo:GSE6791 not downloaded", "asset:data:geo:GSE6791 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "differential_expression", "specific": "limma_voom", "label": "Differential expression analysis", "dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["count_matrix_with_condition"], 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