Abstract

BackgroundThe morbidity and mortality of endometrial tumors, a common type of malignant cancer in women, have increased in recent years. POLE encodes the DNA polymerase ε, which is responsible for the leading strand DNA replication. Somatic mutations of POLE have been acknowledged in numerous cancers, resulting in the accumulation of DNA errors, leading to ultra-mutated tumors. Mutations in the exonuclease domain of POLE have been reported to improve progression-free survival in endometrial cancer. However, the potential relationship and underlying mechanism between POLE mutations and the prognosis of endometrial cancer patients remains unclear.MethodsThe whole exome sequencing data, RNA sequencing data, and clinical information were obtained from the TCGA database and employed for the analyses in this study. The detailed mutational information was analyzed using whole exome sequencing data and the mutated genes were shown with OncoPlot. The survival curves and cox proportional hazards regression analysis were used to accessed patient prognosis, the association of clinical characteristics and prognosis. Differentially expressed genes were analyzed by the edgeR R/Bioconductor package, then the GSEA Pre-ranked tool was used for Gene Set Enrichment Analysis (GSEA) to estimate the function of genes. Expression values were clustered using hierarchical clustering with Euclidean distance and ward linkage by the dendextend R package.ResultsPOLE mutational status was proven to be an independent prognostic factor for endometrial cancer patients. Patients with somatic POLE mutations presented a favorable prognosis. POLE mutations regulated glycolysis and cytokine secretion, affecting cell metabolism and immune response. Autocrine motility factor (AMF)/PGI and AMFR/gp78 exhibited higher expression levels in POLE mutant patients. The comprehensive high expressions of AMFR/gp78 and low expression of POLE were associated with the favorable prognosis of endometrial cancer patients.ConclusionsThis study showed the POLE mutations a vital factor in endometrial cancer patients, leading to a higher expression of AMF/PGI and AMFR/gp78. These results suggested comprehensive consideration of the POLE mutations, expression of AMF/PGI and AMFR/gp78 may provide a more feasible and effective approach for the treatment of endometrial cancer, which might improve the prognosis.

Highlights

  • The morbidity and mortality of endometrial tumors, a common type of malignant cancer in women, have increased in recent years

  • Polymerase ɛ (POLE) mutations regulate Autocrine motility factor (AMF)/Phosphoglucose isomerase (PGI)–AMFR/gp78 expression and patient favorable prognosis To a certain extent, the results of this study have demonstrated that POLE mutations may impact endometrial cancer patient prognosis by regulating cellular glucose metabolism

  • POLE exonuclease domain mutations have been reported to have a benign effect on prognosis in patients with endometrial cancer, little is known about the relationship and possible mechanism between the POLE mutational status and endometrial cancer patient prognosis

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Summary

Introduction

The morbidity and mortality of endometrial tumors, a common type of malignant cancer in women, have increased in recent years. Mutations in the exonuclease domain of POLE have been reported to improve progression-free survival in endometrial cancer. The potential relationship and underlying mechanism between POLE mutations and the prognosis of endometrial cancer patients remains unclear. Endometrial cancer (EC), arising from the lining of the uterus, is one of the most common malignancy among women in developed countries. The mutation frequency profile was related to different ethnicities and tumor grades in endometrial cancer patients [6]. PIK3CA, ARID1A, TP53, PIK3R1, and MUC16 are the most frequent mutations in endometrial cancer patients, and all of them have been reported to be associated with prognosis. PIK3CA, ARID1A, and MUC16 mutations were correlated with favorable prognosis, whereas TP53 and PIK3R1 mutations were correlated with poor prognosis [6, 7]

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