High expression levels of S1PR3 and PDGFRB indicates unfavorable clinical outcomes in colon adenocarcinoma
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Summary
This summary is machine-generated.Sphingosine kinase 1 (SPHK1) and platelet-derived growth factor receptors (PDGFRs) are upregulated in colon adenocarcinoma (COAD), correlating with poor prognosis and increased metastasis. These findings suggest SPHK1/S1PRs and PDGFRs as potential biomarkers for COAD.
Area Of Science
- Oncology
- Molecular Biology
- Genomics
Background
- Sphingosine kinase 1 (SPHK1)/sphingosine 1-phosphate receptors (S1PRs) and platelet-derived growth factor receptors (PDGFRs) are implicated in tumor development.
- The specific roles and clinical significance of these pathways in colon adenocarcinoma (COAD) remain largely uncharacterized.
Purpose Of The Study
- To investigate the expression patterns of SPHK1/S1PRs and PDGFRs in COAD.
- To evaluate the prognostic value of these markers in COAD patients.
- To explore potential therapeutic targets and diagnostic biomarkers for COAD.
Main Methods
- Utilized The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases for expression analysis.
- Performed Kaplan-Meier survival, Spearman's correlation, and χ2 tests to assess prognostic and clinical correlations.
- Employed Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Least Absolute Shrinkage and Selection Operator (LASSO) regression for pathway and biomarker identification.
Main Results
- SPHK1 and PDGFRB showed significant upregulation in COAD tissues, correlating with shorter overall survival (OS).
- High expression of S1PR3 and PDGFRB was associated with advanced N stage and lymph node invasion.
- A five-hub gene prognostic model (SFRP2, GPRC5B, RSPO3, FGF14, TCF7L1) demonstrated significant OS prediction and correlated with increased tumor immune cell infiltration.
Conclusions
- S1PR3 and PDGFRB may serve as critical biomarkers for predicting lymphatic metastasis and poor prognosis in COAD.
- The identified hub genes and their association with immune cell infiltration offer potential therapeutic avenues.
- Further research into these pathways could lead to improved COAD management strategies.

