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Updated: May 3, 2026

Analyzing Tumor Gene Expression Factors with the CorExplorer Web Portal
Published on: October 11, 2019
Loss of connectivity in cancer co-expression networks
Roberto Anglani1, Teresa M Creanza2, Vania C Liuzzi1
1Institute of Intelligent Systems for Automation, National Research Council, CNR-ISSIA, Bari, Italy.
Abstract:
Differential gene expression profiling studies have lead to the identification of several disease biomarkers. However, the oncogenic alterations in coding regions can modify the gene functions without affecting their own expression profiles. Moreover, post-translational modifications can modify the activity of the coded protein without altering the expression levels of the coding gene, but eliciting variations to the expression levels of the regulated genes. These considerations motivate the study of the rewiring of networks co-expressed genes as a consequence of the aforementioned alterations in order to complement the informative content of differential expression. We analyzed 339 mRNAomes of five distinct cancer types to find single genes that presented co-expression patterns strongly differentiated between normal and tumor phenotypes. Our analysis of differentially connected genes indicates the loss of connectivity as a common topological trait of cancer networks, and unveils novel candidate cancer genes. Moreover, our integrated approach that combines the differential expression together with the differential connectivity improves the classic enrichment pathway analysis providing novel insights on putative cancer gene biosystems not still fully investigated.
Insights
Cancer gene networks show altered connectivity, revealing new cancer gene candidates. Integrating gene expression and connectivity analysis offers deeper insights into cancer biology.
Area of Science:
- Genomics
- Systems Biology
- Cancer Research
Background:
- Differential gene expression identifies biomarkers but misses alterations affecting gene function or protein activity.
- Oncogenic mutations and post-translational modifications can alter gene networks without changing expression levels.
- Studying co-expressed gene networks provides complementary information to differential expression analysis.
Purpose of the Study:
- To investigate the rewiring of co-expressed gene networks in cancer.
- To identify genes with differentiated co-expression patterns between normal and tumor tissues.
- To complement differential expression analysis with network connectivity insights.
Main Methods:
- Analysis of 339 mRNAomes across five cancer types.
- Identification of differentially connected genes between normal and tumor phenotypes.
- Integration of differential expression and differential connectivity analyses.
Main Results:
- Loss of connectivity is a common topological feature in cancer gene networks.
- Novel candidate cancer genes were identified through network analysis.
- Integrated analysis improved pathway enrichment, revealing new cancer-related biological systems.
Conclusions:
- Network connectivity analysis is crucial for understanding cancer beyond gene expression levels.
- Altered gene network topology is a hallmark of cancer.
- Combining differential expression and connectivity offers a more comprehensive view of cancer gene functions and interactions.
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