A systematic analysis of C5ORF46 in gastrointestinal tumors as a potential prognostic and immunological biomarker
Background: Chromosome 5 open reading frame 46 ( C5ORF46 ), also known as antimicrobial peptide with 64 amino acid residues ( AP-64 ) and skin and saliva-secreted protein 1 ( SSSP1 ), belongs to the family of open reading frame genes and encodes a small exosomal protein. C5ORF46 has been implicated...
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Veröffentlicht in: | Frontiers in genetics 2022-08, Vol.13, p.926943-926943 |
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Sprache: | eng |
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Zusammenfassung: | Background:
Chromosome 5 open reading frame 46 (
C5ORF46
), also known as antimicrobial peptide with 64 amino acid residues (
AP-64
) and skin and saliva-secreted protein 1 (
SSSP1
), belongs to the family of open reading frame genes and encodes a small exosomal protein.
C5ORF46
has been implicated in antibacterial activity and associated with patient prognosis in pancreatic cancer, colorectal cancer, and stomach cancer. These findings highlight the importance of
C5ORF46
in gastrointestinal (GI) tumor inception and development. However, the prognostic and immunological value of
C5ORF46
in human GI tumors remains largely unknown. In this study, we sought to explore the potential value of
C5ORF46
in GI tumor prognosis and immunology.
Method:
RNA sequencing (RNA-seq) was performed on the tumor and tumor-adjacent normal samples we collected to identify potential target genes for GI tumors. Apart from our RNA-seq data, all original data were downloaded from The Cancer Genome Atlas (TCGA) database and integrated
via
Strawberry Perl (v 5.32.0) and R (v 4.1.1). The differential expression of
C5ORF46
was examined with Oncomine, Tumor Immune Estimation Resource (TIMER), Gene Expression Profiling Interactive Analysis (GEPIA), Cancer Cell Line Encyclopedia (CCLE), the Human Protein Atlas (HPA) and TCGA databases. The c-BioPortal database was used to investigate the genomic alterations of
C5ORF46
. The effect of
C5ORF46
on prognosis and clinical phenotypes was explored
via
bioinformatics analyses on the TCGA and GEPIA databases. We used the bioinformatics analyses based on the TCGA database to analyze tumor mutational burden (TMB), microsatellite instability (MSI), tumor immune cell infiltration, and the correlations between
C5ORF46
expression and several immune-related genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis was carried out
via
the DAVID website and presented as bubble charts using ShengXinRen online tools. Gene set enrichment analysis (GSEA) was performed using R scripts based on data downloaded from the GSEA website. Immunohistochemistry (IHC) was used to validate the expression of
C5ORF46
in GI tumors.
Results:
The results of our RNA-seq data indicated a critical role for
C5ORF46
in colon carcinogenesis. Consistently, we demonstrated that
C5ORF46
was highly expressed in tumor tissues compared to normal tissues in human GI tumors. Moreover, a strong correlation was observed between
C5ORF46
expression levels and patient progn |
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ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2022.926943 |