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Published on: May 17, 2020
Identification modules of gastric cancer based on protein-protein interaction networks and gene expression data
Wei Cui1, Zhenfang Gu, Haiying Liu
1Department of Oncology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, P.R. China.
Purpose:
The tumorigenesis of gastric cancer is an intricate process which contains genetic and epigenetic changes of proto-oncogenes and cancer-suppressor genes. The purpose of this study was to identify novel modules for gastric cancer based on protein-protein interaction networks and gene expression data.
Methods:
Microarray data and corresponding annotated files of E-GEOD-15460 were downloaded from ArrayExpress database. All human protein-protein interactions were downloaded from STRING database. The fast depth-first assay was used to identify all maximal cliques of disease group and control group. Benjamini-Hochberg method was used to perform multiple corrections of p value.
Results:
248 modules for the control group and 30 modules for the disease group were determined in this research, and 734 pairs of similar or same modules of these two groups were detected through calculating module correlation density. Protein-protein interaction (PPI) network was identified, which comprised of 7899 genes and 48469 interrelationship pairs of genes. Finally, 6 modules with remarkable difference were found to be closely related with gastric cancer.
Conclusions:
Novel modules with significant difference and the related genes are useful biomarkers and therapeutic targets for gastric cancer.
Insights
This study identified novel molecular modules in gastric cancer using protein-protein interaction networks and gene expression data. These modules offer potential biomarkers and therapeutic targets for this complex disease.
Area of Science:
- Oncology
- Bioinformatics
- Systems Biology
Background:
- Gastric cancer development involves complex genetic and epigenetic alterations.
- Understanding these changes requires analyzing gene interactions and expression patterns.
Purpose of the Study:
- To identify novel molecular modules associated with gastric cancer.
- To utilize protein-protein interaction networks and gene expression data for this identification.
Main Methods:
- Downloaded microarray data (E-GEOD-15460) and protein-protein interaction data (STRING).
- Employed a fast depth-first assay to detect maximal cliques in disease and control groups.
- Applied Benjamini-Hochberg correction for multiple testing.
Main Results:
- Identified 248 modules in the control group and 30 in the disease group.
- Detected 734 similar/identical modules between groups via correlation density.
- Constructed a protein-protein interaction network with 7899 genes and 48469 interactions.
- Found 6 significantly different modules linked to gastric cancer.
Conclusions:
- Identified novel modules with significant differences in gastric cancer.
- These modules and their associated genes represent potential biomarkers.
- These findings suggest new therapeutic targets for gastric cancer treatment.
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