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基于少突胶质细胞瘤1p/19q共缺失的不同肿瘤环境特征的竞争性内源RNA网络分析

CeRNA Network Analysis Representing Characteristics of Different Tumor Environments Based on 1p/19q Codeletion in Oligodendrogliomas.

作者信息

Ahn Ju Won, Park YoungJoon, Kang Su Jung, Hwang So Jung, Cho Kyung Gi, Lim JaeJoon, Kwack KyuBum

机构信息

Department of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.

Department of Neurosurgery, Bundang CHA Medical Center, CHA University School of Medicine, Seongnam 13496, Korea.

出版信息

Cancers (Basel). 2020 Sep 7;12(9):2543. doi: 10.3390/cancers12092543.

Abstract

Oligodendroglioma (OD) is a subtype of glioma occurring in the central nervous system. The 1p/19q codeletion is a prognostic marker of OD with an isocitrate dehydrogenase () mutation and is associated with a clinically favorable overall survival (OS); however, the exact underlying mechanism remains unclear. Long non-coding RNAs (lncRNAs) have recently been suggested to regulate carcinogenesis and prognosis in cancer patients. Here, we performed in silico analyses using low-grade gliomas from datasets obtained from The Cancer Genome Atlas to investigate the effects of ceRNA with 1p/19q codeletion on ODs. Thus, we selected modules of differentially expressed genes that were closely related to 1p/19q codeletion traits using weighted gene co-expression network analysis and constructed 16 coding RNA-miRNA-lncRNA networks. The ceRNA network participated in ion channel activity, insulin secretion, and collagen network and extracellular matrix (ECM) changes. In conclusion, ceRNAs with a 1p/19q codeletion can create different tumor microenvironments via potassium ion channels and ECM composition changes; furthermore, differences in OS may occur. Moreover, if extrapolated to gliomas, our results can provide insights into the consequences of identical gene expression, indicating the possibility of tracking different biological processes in different subtypes of glioma.

摘要

少突胶质细胞瘤(OD)是发生于中枢神经系统的一种胶质瘤亚型。1p/19q共缺失是伴有异柠檬酸脱氢酶()突变的OD的一个预后标志物,且与临床良好的总生存期(OS)相关;然而,确切的潜在机制仍不清楚。最近有研究表明长链非编码RNA(lncRNA)可调控癌症患者的肿瘤发生和预后。在此,我们利用从癌症基因组图谱获得的数据集中的低级别胶质瘤进行了计算机分析,以研究具有1p/19q共缺失的竞争性内源RNA(ceRNA)对OD的影响。因此,我们使用加权基因共表达网络分析选择了与1p/19q共缺失特征密切相关的差异表达基因模块,并构建了16个编码RNA-微小RNA(miRNA)-lncRNA网络。该ceRNA网络参与了离子通道活性、胰岛素分泌以及胶原网络和细胞外基质(ECM)的变化。总之,具有1p/19q共缺失的ceRNA可通过钾离子通道和ECM组成变化产生不同的肿瘤微环境;此外,可能会出现OS差异。而且,如果将我们的结果外推至胶质瘤,可深入了解相同基因表达的后果,这表明在不同亚型的胶质瘤中追踪不同生物学过程的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eff7/7564449/0ef167beaa6a/cancers-12-02543-g001.jpg

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