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Prognostic Signatures of Metabolic Genes and Metabolism-Related Long Non-coding RNAs Accurately Predict Overall Survival for Osteosarcoma Patients

机译:代谢基因的预后签名和新陈代谢相关的长期非编码RNA准确地预测骨肉瘤患者的整体存活

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In this study, data of osteosarcoma (OS) tissue and normal muscle tissue from Therapeutically Applicable Research to Generate Effective Treatments (TARGET) (n =84) and GTEx database (n =396), eight survival‐related metabolic genes were identified in differentially expressed metabolic genes by univariate Cox regression analysis. Six metabolic genes were screened to prognostic signature by LASSO regression analysis. The metabolism gene signature has a good performance in predicting survival of OS patients and is also an independent prognostic factor. Next, eight metabolism‐related long non‐coding RNAs (lncRNAs) were also identified the metabolism‐related lncRNA signature and can accurately predict overall survival for. Gene set enrichment analysis (GSEA) and Gene Set Variation Analysis (GSVA) showed that multiple metabolism processes and signalling pathways are enriched in the high‐risk and low‐risk group. Immunization scores analysis showed that there is lower score in high-risk group than low-risk groups. These results showed that Six metabolic genes and eight metabolism‐related prognostic lncRNAs signature have good performance in predicting the survival outcomes of OS patients.
机译:在本研究中,骨肉瘤(OS)组织和正常肌肉组织的数据来自治疗上适用的研究,以产生有效治疗(靶)(n = 84)和GTEX数据库(n = 396),差异鉴定了8个生存相关的代谢基因单变量COX回归分析表达代谢基因。通过套索回归分析筛选六种代谢基因以预后签名。代谢基因特征在预测OS患者的存活方面具有良好的性能,也是一个独立的预后因素。接下来,还鉴定了八个与新陈代谢相关的长编码RNA(LNCRNA)鉴定了与之相关的LNCRNA签名,可以准确地预测整体存活。基因设定富集分析(GSEA)和基因设定变异分析(GSVA)表明,高风险和低风险组中富集了多种代谢过程和信号通路。免疫分数分析表明,高风险群体的得分低于低风险群体。这些结果表明,六种代谢基因和八种新陈代谢相关的预后LNCRNA签名具有良好的性能,可预测OS患者的存活结果。

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