Identification of Core Prognosis-Related Candidate Genes in Chinese Gastric Cancer Population Based on Integrated Bioinformatics

Abstract EN

Background.

Gastric cancer (GC) is one of the leading causes of cancer-related mortality worldwide.

There are great geographical differences in the incidence of GC, and somatic mutation rates of driver genes are also different.

The present study is aimed at screening core prognosis-related candidate genes in Chinese gastric cancer population based on integrated bioinformatics for the early diagnosis and prognosis of GC.

Methods.

In the present study, the differentially expressed genes (DEGs) in GC were identified using four microarray datasets from the Gene Expression Omnibus (GEO) database.

The samples of these datasets were all from China.

Functional enrichment analysis of DEGs was conducted to evaluate the underlying molecular mechanisms involved in GC.

Protein-protein interaction (PPI) network and cytoHubba were performed to determine hub genes associated with GC.

Gene Expression Profiling Interactive Analysis (GEPIA) and Human Protein Atlas (HPA) were performed to validate the hub genes.

Results.

A total of 240 DEGs were obtained through the RRA method, including 80 upregulated genes and 160 downregulated genes.

Upregulated genes were mainly enriched in extracellular matrix organization, extracellular matrix, and extracellular matrix structural constituent.

The downregulated genes were mainly enriched in digestion, extracellular space, and oxidoreductase activity.

The KEGG pathway enrichment analysis showed that the upregulated genes were mainly associated with ECM-receptor interaction, focal adhesion, and PI3K-Akt signaling pathway.

And downregulated genes were mainly associated with the metabolism of xenobiotics by cytochrome P450, metabolic pathways, and gastric acid secretion.

The transcriptional and translational expression levels of the genes including COL1A1, COL5A2, COL12A1, and VCAN were higher in GC tissues than normal tissues.

Conclusion.

A total of four genes including COL1A1, COL5A2, COL12A1, and VCAN were considered potential GC biomarkers in the Chinese population.

And ECM-receptor interaction, focal adhesion, and PI3K-Akt signaling pathway were revealed to be important mechanisms of GC.

Our findings provide novel insights into the occurrence and progression of GC in the Chinese population.