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pmid:34795689

Meta-Analysis of Esophageal Cancer Transcriptomes Using Independent Component Analysis.

Ainur Ashenova · Asset Daniyarov · Askhat Molkenov · Aigul Sharip · Andrei Zinovyev · Ulykbek Kairov

Frontiers in genetics · 2021 doi:10.3389/fgene.2021.683632

Paper

complete

Experiment

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Data

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Analysis

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Execution

absent

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title
Meta-Analysis of Esophageal Cancer Transcriptomes Using Independent Component Analysis.
doi
10.3389/fgene.2021.683632
pmid
34795689
authors array · 6 items
[0]
Ainur Ashenova
[1]
Asset Daniyarov
[2]
Askhat Molkenov
[3]
Aigul Sharip
[4]
Andrei Zinovyev
[5]
Ulykbek Kairov
journal
Frontiers in genetics
year
2021
abstract
Independent Component Analysis is a matrix factorization method for data dimension reduction. ICA has been widely applied for the analysis of transcriptomic data for blind separation of biological, environmental, and technical factors affecting gene expression. The study aimed to analyze the publicly available esophageal cancer data using the ICA for identification and comprehensive analysis of reproducible signaling pathways and molecular signatures involved in this cancer type. In this study, four independent esophageal cancer transcriptomic datasets from GEO databases were used. A bioinformatics tool « BiODICA-Independent Component Analysis of Big Omics Data» was applied to compute independent components (ICs). Gene Set Enrichment Analysis (GSEA) and ToppGene uncovered the most significantly enriched pathways. Construction and visualization of gene networks and graphs were performed using the Cytoscape, and HPRD database. The correlation graph between decompositions into 30 ICs was built with absolute correlation values exceeding 0.3. Clusters of components-pseudocliques were observed in the structure of the correlation graph. The top 1,000 most contributing genes of each ICs in the pseudocliques were mapped to the PPI network to construct associated signaling pathways. Some cliques were composed of densely interconnected nodes and included components common to most cancer types (such as cell cycle and extracellular matrix signals), while others were specific to EC. The results of this investigation may reveal potential biomarkers of esophageal carcinogenesis, functional subsystems dysregulated in the tumor cells, and be helpful in predicting the early development of a tumor.
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ICA was applied to each transcriptomic dataset separately.
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In this study, four independent esophageal cancer transcriptomic datasets from GEO databases were used.
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sections[0] "Abstract" paragraph 1
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A bioinformatics tool « BiODICA—Independent Component Analysis of Big Omics Data» was applied to compute independent components (ICs).
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ICA was applied to four publicly available esophageal cancer transcriptomic datasets from GEO to compute independent components and identify reproducible signaling pathways and molecular signatures.
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title
Gene expression profiling of esophageal squamous cell carcinomas
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2026-11-01T17:30:42Z
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ICA was applied to each transcriptomic dataset separately.
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Complete file
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ICA has been widely applied for the analysis of transcriptomic data for blind separation of biological, environmental, and technical factors affecting gene expression. The study aimed to analyze the publicly available esophageal cancer data using the ICA for identification and comprehensive analysis of reproducible signaling pathways and molecular signatures involved in this cancer type. In this study, four independent esophageal cancer transcriptomic datasets from GEO databases were used. A bioinformatics tool « BiODICA-Independent Component Analysis of Big Omics Data» was applied to compute independent components (ICs). Gene Set Enrichment Analysis (GSEA) and ToppGene uncovered the most significantly enriched pathways. Construction and visualization of gene networks and graphs were performed using the Cytoscape, and HPRD database. The correlation graph between decompositions into 30 ICs was built with absolute correlation values exceeding 0.3. Clusters of components-pseudocliques were observed in the structure of the correlation graph. The top 1,000 most contributing genes of each ICs in the pseudocliques were mapped to the PPI network to construct associated signaling pathways. Some cliques were composed of densely interconnected nodes and included components common to most cancer types (such as cell cycle and extracellular matrix signals), while others were specific to EC. 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