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免疫基因组分析表明AC003092.1是多形性胶质母细胞瘤中一种与免疫相关的增强子RNA。

Immunogenomic Profiling Demonstrate AC003092.1 as an Immune-Related eRNA in Glioblastoma Multiforme.

作者信息

Guo Xiao-Yu, Zhong Sheng, Wang Zhen-Ning, Xie Tian, Duan Hao, Zhang Jia-Yu, Zhang Guan-Hua, Liang Lun, Cui Run, Hu Hong-Rong, Lu Jie, Wu Yi, Dong Jia-Jun, He Zhen-Qiang, Mou Yong-Gao

机构信息

Department of Neurosurgery/Neuro-oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer, Guangzhou, China.

The First Clinical Medical College of Yunnan University of Traditional Chinese Medicine, Kunming, China.

出版信息

Front Genet. 2021 Mar 18;12:633812. doi: 10.3389/fgene.2021.633812. eCollection 2021.

Abstract

Enhancer RNAs, a type of long non-coding RNAs (lncRNAs), play a critical role in the occurrence and development of glioma. RNA-seq data from 161 glioblastoma multiforme (GBM) samples were acquired from The Cancer Genome Atlas database. Then, 70 eRNAs were identified as prognosis-related genes, which had significant relations with overall survival (log-rank test, < 0.05). AC003092.1 was demonstrated as an immune-related eRNA by functional enrichment analysis. We divided samples into two groups based on AC003092.1 expression: AC003092.1 High (AC003092.1_H) and AC003092.1 Low (AC003092.1_L) and systematically analyzed the influence of AC003092.1 on the immune microenvironment by single-sample gene-set enrichment analysis and CIBERSORTx. We quantified AC003092.1 and TFPI2 levels in 11 high-grade gliomas, 5 low-grade gliomas, and 7 GBM cell lines. Our study indicates that AC003092.1 is related to glioma-immunosuppressive microenvironment, and these results offer innovative sights into GBM immune therapy.

摘要

增强子RNA是一类长链非编码RNA(lncRNA),在胶质瘤的发生发展中起关键作用。从癌症基因组图谱数据库获取了161例多形性胶质母细胞瘤(GBM)样本的RNA测序数据。然后,70种增强子RNA被鉴定为与预后相关的基因,它们与总生存期有显著相关性(对数秩检验,<0.05)。通过功能富集分析证明AC003092.1是一种与免疫相关的增强子RNA。我们根据AC003092.1的表达将样本分为两组:AC003092.1高表达组(AC003092.1_H)和AC003092.1低表达组(AC003092.1_L),并通过单样本基因集富集分析和CIBERSORTx系统分析了AC003092.1对免疫微环境的影响。我们对11例高级别胶质瘤、5例低级别胶质瘤和7种GBM细胞系中的AC003092.1和TFPI2水平进行了定量。我们的研究表明AC003092.1与胶质瘤免疫抑制微环境相关,这些结果为GBM免疫治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08ce/8012670/0fc0fa56e6fd/fgene-12-633812-g001.jpg

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