Abstract

PurposeA thymoma is a tumor arising from the epithelium of the thymus, mostly occurring in the anterior mediastinum. The incidence of this disease is low and research progress in this field is slow. Consequently, there is an urgent need to investigate the correlation between molecular regulation and the prediction of survival and prognosis in patients with thymoma.MethodsWe collected thymoma datasets from The Cancer Genome Atlas (TCGA). Differentially expressed genes (DEGs) of TCGA datasets were then determined using R software. A gene signature was obtained by screening prognostic DEGs from the TCGA datasets using univariate and multivariate Cox survival analysis. The summation of the weighted expression levels was calculated as a risk score, which could then be used to predict the survival rate and prognosis of patients with thymoma. The validity of this model was verified by the analysis of receiver operating characteristic (ROC) curves and area under the curve (AUC).ResultsIn total, 297 DEGs were identified from the integrated results of TCGA datasets. A seven-gene signature, along with a regression model of prognostic risk, was obtained by Cox survival analysis. The expression levels of the seven genes were then weighted and summed to calculate the risk score for each sample. Patients were effectively divided into high- and low-risk groups using the median risk score (P < 0.05). ROC analysis showed that this Cox regression model was effective in predicting the prognosis of patients with thymus tumors (AUC = 0.983, P < 0.05).ConclusionFor the first time, we identified an effective seven-gene signature in patients with thymic tumors. In the future, the risk and prognosis of patients can be preliminarily assessed using this model, although further testing is required to improve rigor.

Highlights

  • Thymoma arises from the thymic epithelial cells and accounts for approximately 20% of anterior mediastinal tumors, making this the most common tumor

  • Genomic mRNA-seq expression data and clinical thymoma materials were downloaded from the The Cancer Genome Atlas (TCGA) database website

  • Differentially expressed genes (DEGs) enrichment analysis was performed in the Kyoko Encyclopedia of Genes and Genomes (KEGG) database, and the signaling pathway characteristics of DEGs were demonstrated by visualization graphics

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Summary

Introduction

Thymoma arises from the thymic epithelial cells and accounts for approximately 20% of anterior mediastinal tumors, making this the most common tumor. The annual incidence of thymoma is approximately 0.13/100,000, with the onset age ranging from 30 to 50 years (Strobel et al.2010; Girard et al 2009). The prognosis of patients with thymoma is largely determined by the thymoma histological type, which is complex. This complexity has led to the present lack of uniform measurement standards. The classification of thymoma by the World Health Organization (WHO) is largely based on the proportion of lymphocytes in the thymus tumor. WHO classification type A (medullary type) and type B1 are considered to be less invasive, while type B3

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