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用于预测低级别胶质瘤总生存期的糖酵解相关基因特征的构建与验证

Construction and Verification of a Glycolysis-Associated Gene Signature for the Prediction of Overall Survival in Low Grade Glioma.

作者信息

Liu Wei, Liu Chunshan, Chen Chengcong, Huang Xiaoting, Yi Qi, Tian Yunhong, Peng Biao, Yuan Yawei

机构信息

Department of Radiation Oncology, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.

Department of Neurosurgery, Affiliated Cancer Hospital and Institute of Guangzhou Medical University, Guangzhou, China.

出版信息

Front Genet. 2022 Mar 23;13:843711. doi: 10.3389/fgene.2022.843711. eCollection 2022.

Abstract

The overall survival of patients with lower grade glioma (LGG) that might develop into high-grade malignant glioma shows marked heterogeneity. The currently used clinical evaluation index is not sufficient to predict precise prognostic outcomes accurately. To optimize survival risk stratification and the personalized management of patients with LGG, there is an urgent need to develop an accurate risk prediction model. The TCGA-LGG dataset, downloaded from The Cancer Genome Atlas (TCGA) portal, was used as a training cohort, and the Chinese Glioma Genome Atlas (CGGA) dataset and Rembrandt dataset were used as validation cohorts. The levels of various cancer hallmarks were quantified, which identified glycolysis as the primary overall survival-related risk factor in LGGs. Furthermore, using various bioinformatic and statistical methods, we developed a strong glycolysis-related gene signature to predict prognosis. Gene set enrichment analysis showed that in our model, high-risk glioma correlated with the chemoradiotherapy resistance and poor survival. Moreover, based on established risk model and other clinical features, a decision tree and a nomogram were built, which could serve as useful tools in the diagnosis and treatment of LGGs. This study indicates that the glycolysis-related gene signature could distinguish high-risk and low-risk patients precisely, and thus can be used as an independent clinical feature.

摘要

可能发展为高级别恶性胶质瘤的低级别胶质瘤(LGG)患者的总生存期存在显著异质性。目前使用的临床评估指标不足以准确预测精确的预后结果。为了优化LGG患者的生存风险分层和个性化管理,迫切需要开发一种准确的风险预测模型。从癌症基因组图谱(TCGA)门户下载的TCGA-LGG数据集用作训练队列,中国胶质瘤基因组图谱(CGGA)数据集和伦勃朗数据集用作验证队列。对各种癌症特征水平进行了量化,确定糖酵解是LGG中主要的总生存相关风险因素。此外,使用各种生物信息学和统计方法,我们开发了一个强大的糖酵解相关基因特征来预测预后。基因集富集分析表明,在我们的模型中,高危胶质瘤与放化疗耐药性和较差的生存率相关。此外,基于建立的风险模型和其他临床特征,构建了决策树和列线图,可作为LGG诊断和治疗的有用工具。这项研究表明,糖酵解相关基因特征可以精确区分高危和低危患者,因此可作为一种独立的临床特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94dd/8983898/35804fbdfa67/fgene-13-843711-g001.jpg

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