Key result
High APOC1 expression was significantly associated with poorer overall survival in patients with esophageal squamous cell carcinoma (HR 2.96).
Why the study?
Does APOC1 expression level predict prognosis and correlate with immune infiltration in patients with esophageal squamous cell carcinoma?
Observational (n=94)
Does APOC1 expression level predict prognosis and correlate with immune infiltration in patients with esophageal squamous cell carcinoma?
Hazard Ratio: 2.96 (95% CI 1.27–6.88)
p-value: p=0.0089
Increased expression of APOC1 is an independent indicator of poor overall survival and correlates with immune infiltration in esophageal squamous cell carcinoma.
APOC1 overexpression may aid ESCC prognostication; observational data leave open clinical adoption pending prospective validation.
PurposeEsophageal cancer (EC) is the sixth leading cause of cancer death worldwide. Esophageal squamous cell carcinoma (ESCC) is a predominant subtype of EC. Identifying diagnostic biomarkers for ESCC is necessary for cancer practice. Increasing evidence illustrates that apolipoprotein C-1 (APOC1) participates in the carcinogenesis. However, the biological function of APOC1 in ESCC remains unclear. Patients and methodsWe investigated the expression level of APOC1 using TIMER2.0 and GEO databases, the prognostic value of APOC1 in ESCC using Kaplan-Meier plotter and TCGA databases. We used LinkedOmics to identify co-expressed genes with APOC1 and perform GO and KEGG pathway analysis. The target networks of kinases, miRNAs and transcription factors were predicted by gene set enrichment analysis (GSEA). The correlations between APOC1 and immune infiltration were calculated using TIMER2.0 and CIBERSORT databases. We further performed the prognostic analysis based on APOC1 expression levels in related immune cells subgroups via Kaplan-Meier plotter database. ResultsAPOC1 was found overexpressed in tumor tissues in multiple ESCC cohorts and high APOC1 expression was related to a dismal prognosis. Multivariate analysis confirmed that APOC1 overexpression was an independent indicator of poor OS. Functional network analysis indicated that APOC1 might regulate the natural killer cell mediated cytotoxicity, phagosome, AMPK and hippo signaling through pathways involving some cancer-related kinases, miRNA and transcription factors. Immune infiltration analysis showed that APOC1 was significantly positively correlated with M0 macrophages cells, M1 macrophages cells and activated NK cells, negatively correlated with regulatory T cells, CD8 T cells, neutrophils and monocytes. High APOC1 expression had a poor prognosis in server immune cells subgroups in ESCC, including decreased CD8+ T cells subgroups. ConclusionThese findings suggest that increased expression of APOC1 is related to poor prognosis and immune infiltration in ESCC. APOC1 holds promise for serving as a valuable diagnostic and prognostic marker in ESCC.
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Xie et al. (2020) conducted an observational in Esophageal squamous cell carcinoma (ESCC) (n=94). High APOC1 expression vs. Low APOC1 expression was evaluated on Overall survival (OS) (HR 2.96, 95% CI 1.27-6.88, p=0.0089). High APOC1 expression was significantly associated with poorer overall survival in patients with esophageal squamous cell carcinoma (HR 2.96).
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