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Identification of an ATP metabolism‐related signature associated with prognosis and immune microenvironment in gliomas

机译:鉴定胶质瘤中与预后和免疫微环境相关的ATP新陈代谢相关签名

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摘要

As the core element of material and energy metabolism pathways, the biological functions and prognostic significance of ATP metabolism in diffuse gliomas have so far remained unclear. Based on comprehensive analysis of ATP metabolism‐related gene expression profiles, we constructed an ATP metabolism‐related risk signature to determine the role of ATP metabolism. We found that this ATP metabolism‐related gene expression profile could divide patients into 2 robust groups with distinct clinical characteristics and prognosis. Patients in the high‐risk group tended to be predicted as malignant entities, indicating that the activation of ATP metabolism may promote the malignant progress of diffuse gliomas. Cox regression and Kaplan‐Meier analyses suggested that this risk signature was an independent predictor for prognosis. Furthermore, we constructed an individualized prognosis prediction model through nomogram and time‐dependent receiver operating characteristic (ROC) curve analyses. Functional analysis suggested that, in addition to material and energy metabolism, ATP metabolism also played an essential role in the regulation of the tumor immune microenvironment. In brief, the ATP metabolism‐related signature was tightly associated with regulation of the tumor immune microenvironment and could serve as an independent prognostic biomarker in diffuse gliomas.
机译:作为材料和能量代谢途径的核心元素,到目前为止,ATP代谢在弥漫性胶质瘤中的生物学功能和预后意义仍不清楚。基于ATP新陈代谢相关基因表达谱的综合分析,我们构建了ATP新陈代谢相关的风险签名,以确定ATP新陈代谢的作用。我们发现,该ATP新陈代谢相关的基因表达谱可以将患者分为2种强大的临床特征和预后。高风险组的患者倾向于预测为恶性实体,表明ATP代谢的激活可以促进弥漫性胶质瘤的恶性进展。 COX回归和Kaplan-Meier分析表明,这种风险签名是预后的独立预测因素。此外,我们通过NOMO图和时间依赖的接收器操作特征(ROC)曲线分析构建了个性化预测预测模型。功能分析表明,除了材料和能量代谢外,ATP代谢也在调节肿瘤免疫微环境中起重要作用。简而言之,ATP新陈代谢相关的签名与肿瘤免疫微环境的调节紧密相关,并且可以作为弥漫性胶质瘤的独立预后生物标志物。

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