Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China.
Department of Orthopedics, JXHC Key Laboratory of Digital Orthopedics, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Nanchang, Jiangxi, China.
PLoS One. 2024 Mar 1;19(3):e0299720. doi: 10.1371/journal.pone.0299720. eCollection 2024.
Ewing's sarcoma (ES) is the second most common bone and soft tissue malignancy in children and adolescents with a poor prognosis. The identification of genes with prognostic value may contribute to the prediction and treatment of this disease. The GSE17679, GSE68776, GSE63155, and GSE63156 datasets were downloaded from the Gene Expression Omnibus database and qualified. Prognostic value of differentially expressed genes (DEGs) between the normal and tumor groups and immune cell infiltration were explored by several algorithms. A prognostic model was established and validated. Finally, functional analyses of the DEGs were performed. Proline rich 11 (PRR11) and mast cell infiltration were noted as the key indicators for the prognosis of ES. Kaplan-Meier and scatter plots for the training and two validation sets showed that patients in the low-PRR11 expression group were associated with better outcomes than those in the high-PRR11 expression group. The concordance indices and calibration analyses of the prognostic model indicated good predictive accuracy in the training and validation sets. The area under the curve values obtained through the receiver operating characteristic analysis for 1-, 3-, 5-year prediction were ≥ 0.75 in the three cohorts, suggesting satisfactory sensitivity and specificity of the model. Decision curve analyses suggested that patients could benefit more from the model than the other strategies. Functional analyses suggested that DEGs were mainly clustered in the cell cycle pathway. PRR11 and mast cell infiltration are potential prognostic indicators in ES. PRR11 possibly affects the prognosis of patients with ES through the cell cycle pathway.
尤因氏肉瘤(ES)是儿童和青少年中第二常见的骨和软组织恶性肿瘤,预后不良。鉴定具有预后价值的基因可能有助于预测和治疗这种疾病。从基因表达综合数据库中下载了 GSE17679、GSE68776、GSE63155 和 GSE63156 数据集,并进行了质量控制。通过多种算法探讨了正常组和肿瘤组之间差异表达基因(DEGs)的预后价值和免疫细胞浸润。建立并验证了预后模型。最后,对 DEGs 进行了功能分析。脯氨酸丰富蛋白 11(PRR11)和肥大细胞浸润被认为是 ES 预后的关键指标。训练集和两个验证集的 Kaplan-Meier 和散点图显示,PRR11 低表达组患者的预后明显优于 PRR11 高表达组。预后模型的一致性指数和校准分析表明,在训练集和验证集中具有良好的预测准确性。在三个队列中,通过接收者操作特征分析获得的用于 1 年、3 年和 5 年预测的曲线下面积值均≥0.75,表明该模型具有令人满意的敏感性和特异性。决策曲线分析表明,与其他策略相比,患者可以从该模型中获益更多。功能分析表明,DEGs 主要集中在细胞周期途径。PRR11 和肥大细胞浸润是 ES 的潜在预后指标。PRR11 可能通过细胞周期途径影响 ES 患者的预后。