4.3 Article

Identification of ANXA1 as a potential prognostic biomarker and correlating with immune infiltrates in colorectal cancer

Journal

AUTOIMMUNITY
Volume 54, Issue 2, Pages 76-87

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/08916934.2021.1887148

Keywords

Colorectal cancer; differently expressed genes; underlying mechanisms; prediction model; immune infiltrates

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This study reveals that high expression of ANXA1 is associated with poor prognosis in colorectal cancer patients. Changes in ANXA1 expression are strongly correlated with infiltrating levels of various immune cells in colorectal cancer. Additionally, ANXA1 expression is closely linked to immune cell recruitment, macrophage polarization, and T cell exhaustion markers.
Background ANXA1 is a calcium-dependent phospholipid-binding protein and is frequently associated with inflammation, cell proliferation and apoptosis. However, the relationship between ANXA1 and the prognosis of multiple tumours and tumour infiltrating immune cells remains unclear. Methods Multivariate Cox proportional regression analysis was used for signature genes exploration in the basic of colon adenocarcinoma (COAD) RNA-sequence dataset obtained from TCGA, following the identification of 267 common differentially expressed genes, including ANXA1, among three expression profile datasets (GSE41328, GSE110224, and GSE113513). The differential expression of ANXA1 in different tumours and their corresponding normal tissues were evaluated through the Tumour Immune Estimation Resource (TIMER) and Oncomine database. Subsequently, we investigated the correlation between the expression level of ANXA1 and diverse panel of infiltrating immune cells and their related gene markers in colorectal cancer using correlation analysis in TIMER and GEPIA database. Results The high expression of ANXA1 was demonstrated to be closely correlated with poor survival in patients with colorectal cancer. More importantly, we found that changes in ANXA1 expression showed a moderate to strong, and statistically significant, correlation with infiltrating levels of B cells, CD8+ T cells, CD4+ T cells, macrophages, neutrophils and dendritic cells. By contrast, there are only weak correlations between ANXA1 expression and immune cell infiltration in ESCA and STAD. ANXA1 expression was considerably associated with various immune markers involving immune cell recruitment, polarization of tumour-associated macrophages, and T cell exhaustion. Conclusion ANXA1 is not only an independent risk factor in the prediction of the prognosis of colorectal cancer, but also a crucial regulator in immune cell infiltration. This study may shed light on the clinical value of ANXA1, especially in the areas of early diagnosis of colorectal cancer and therapeutic target discovery.

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