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一种与低级别胶质瘤预后相关的缺氧相关长链非编码RNA特征

A Hypoxia-Related Long Non-Coding RNAs Signature Associated With Prognosis in Lower-Grade Glioma.

作者信息

Feng Qinglin, Qian Cheng, Fan Shibing

机构信息

Department of Neurosurgery, Chongqing University Three Gorges Hospital & Chongqing Three Gorges Central Hospital, Chongqing, China.

Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.

出版信息

Front Oncol. 2021 Nov 19;11:771512. doi: 10.3389/fonc.2021.771512. eCollection 2021.

Abstract

Accumulating evidence suggests that hypoxia microenvironment and long non-coding lncRNAs (lncRNAs) exert critical roles in tumor development. Herein, we aim to develop a hypoxia-related lncRNA (HRL) model to predict the survival outcomes of patient with lower-grade glioma (LGG). The RNA-sequencing data of 505 LGG samples were acquired from The Cancer Genome Atlas (TCGA). Using consensus clustering based on the expression of hypoxia-related mRNAs, these samples were divided into three subsets that exhibit distinct hypoxia content, clinicopathologic features, and survival status. The differentially expressed lncRNAs across the subgroups were documented as candidate HRLs. With LASSO regression analysis, eight informative lncRNAs were selected for constructing the prognostic HRL model. This signature had a good performance in predicting LGG patients' overall survival in the TCGA cohort, and similar results could be achieved in two validation cohorts from the Chinese Glioma Genome Atlas. The HRL model also showed correlations with important clinicopathologic characteristics such as patients' age, tumor grade, IDH mutation, 1p/19q codeletion, MGMT methylation, and tumor progression risk. Functional enrichment analysis indicated that the HLR signature was mainly involved in regulation of inflammatory response, complement, hypoxia, Kras signaling, and apical junction. More importantly, the signature was related to immune cell infiltration, estimated immune score, tumor mutation burden, neoantigen load, and expressions of immune checkpoints and immunosuppressive cytokines. Finally, a nomogram was developed by integrating the HRL signature and clinicopathologic features, with a concordance index of 0.852 to estimate the survival probability of LGG patients. In conclusion, our study established an effective HRL model for prognosis assessment of LGG patients, which may provide insights for future research and facilitate the designing of individualized treatment.

摘要

越来越多的证据表明,缺氧微环境和长链非编码RNA(lncRNA)在肿瘤发展中发挥着关键作用。在此,我们旨在建立一种与缺氧相关的lncRNA(HRL)模型,以预测低级别胶质瘤(LGG)患者的生存结局。从癌症基因组图谱(TCGA)获取了505例LGG样本的RNA测序数据。基于缺氧相关mRNA的表达进行一致性聚类,将这些样本分为三个亚组,它们具有不同的缺氧含量、临床病理特征和生存状态。记录亚组间差异表达的lncRNA作为候选HRL。通过LASSO回归分析,选择了8个信息丰富的lncRNA构建预后HRL模型。该特征在预测TCGA队列中LGG患者的总生存方面表现良好,在中国胶质瘤基因组图谱的两个验证队列中也能得到类似结果。HRL模型还与重要的临床病理特征相关,如患者年龄、肿瘤分级、IDH突变、1p/19q共缺失、MGMT甲基化和肿瘤进展风险。功能富集分析表明,HLR特征主要参与炎症反应、补体、缺氧、Kras信号传导和顶端连接的调节。更重要的是,该特征与免疫细胞浸润

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1a9/8640178/7312ae910bfa/fonc-11-771512-g001.jpg

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