Sequencing and Bioinformatics analysis of lncRNA/circRNA-miRNA-mRNA in Glioblastoma multiforme

被引:5
|
作者
Wang, Renjie [1 ,2 ]
Li, Qi [3 ]
Chu, Xiaolei [3 ]
Li, Nan [2 ]
Liang, Haiqian [2 ]
He, Feng [1 ]
机构
[1] Tianjin Univ, Acad Med Engn & Translat Med, Tianjin 300072, Peoples R China
[2] Characterist Med Ctr Chinese Peoples Armed Police, Dept Neurosurg, Tianjin 300162, Peoples R China
[3] Tianjin Univ, Tianjin Hosp, Tianjin 300050, Peoples R China
基金
中国国家自然科学基金;
关键词
GBM; lncRNA; circRNA-miRNA-mRNA; ceRNA; Bioinformatics; RNA-sequencing; CEACAM5;
D O I
10.1007/s11011-023-01256-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evidence suggests that non-coding RNAs have a role in glioblastoma multiforme (GBM), although the regulatory mechanisms controlled by competing endogenous RNAs (ceRNAs) in GBM are still poorly understood and infrequently described. This research extensively analyzed circRNA, lncRNA, miRNA, and mRNA expression changes in GBM patients. RNA-sequencing analyses were conducted to investigate differentially expressed genes (DEGs), lncRNAs (DELs), miRNAs (DEMs), and circRNAs (DECs) in the GBM. In this study, researchers found that GBM patients and healthy controls differed in the presence of 1224 DECs, 1406 DELs, 229 DEMs, and 2740 DEGs. PPI network analysis demonstrated that CEACAM5, CXCL17, FAM83A, TMPRSS4, and GGPRC5A were hub genes and enriched in modules. Then a ceRNA network was constructed with 8 circRNA, 7 lncRNAs, 16 miRNAs, and 17 mRNAs. Overall, the ceRNA interaction axes that were found may prove to be pivotal therapeutic targets for treating GBM.
引用
收藏
页码:2289 / 2300
页数:12
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