Shi Jiandong, Zhang Piaoyan, Su Huarong, Cai Lingyi, Zhao Liang, Zhou Haixia
Department of Hematology, the Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, People's Republic of China.
Pharmgenomics Pers Med. 2021 Jul 13;14:849-858. doi: 10.2147/PGPM.S312171. eCollection 2021.
To analyze the changes in downstream genes, signaling pathways, and proteins based on the difference of microRNA (miRNA) expression in neuroblastoma (NB).
GSE128004 second-generation sequencing expression data were downloaded from GEO, and Limma package of R language was used to analyze differential expression, and a volcano map and heat map were drawn; the target genes corresponding to the differential miRNA were found using the miWalk web tool, and GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) were performed. The key genes were identified and verified in the TCGA database.
A total of 34 differentially expressed miRNAs were screened out. Among them, 22 up-regulated miRNAs predicted 1163 target genes and 12 down-regulated miRNAs predicted 1474 target genes. Target genes were enriched and analyzed by KEGG to find the FOXO signal pathway, mTOR signal pathway, AMPK signal pathway, and other signal pathways. After GO analysis, axon formation, regulation of chemical synaptic transmitters, regulation of nerve synapses, regulation of cross-synaptic signals, and other physiological processes were assessed. A total of 16 key genes were obtained by PPI analysis, and the survival analysis of TP53 and ATM genes verified in the TCGA database showed statistical significance.
The 34 differential miRNAs may be related to the occurrence and development of NB. TP53 and ATM are related to the prognosis of NB. The role and mechanism of TP53 and ATM in NB need to be further verified.
基于神经母细胞瘤(NB)中微小RNA(miRNA)表达差异分析下游基因、信号通路及蛋白质的变化。
从GEO下载GSE128004二代测序表达数据,使用R语言的Limma包分析差异表达,并绘制火山图和热图;利用miWalk网络工具查找差异miRNA对应的靶基因,并进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析。在TCGA数据库中鉴定并验证关键基因。
共筛选出34个差异表达的miRNA。其中,22个上调的miRNA预测出1163个靶基因,12个下调的miRNA预测出1474个靶基因。通过KEGG对靶基因进行富集分析,发现FOXO信号通路、mTOR信号通路、AMPK信号通路等信号通路。经过GO分析,评估了轴突形成、化学突触传递调节、神经突触调节、跨突触信号调节等生理过程。通过蛋白质-蛋白质相互作用(PPI)分析共获得16个关键基因,在TCGA数据库中对TP53和ATM基因进行的生存分析显示具有统计学意义。
34个差异miRNA可能与NB的发生发展有关。TP53和ATM与NB的预后有关。TP53和ATM在NB中的作用及机制有待进一步验证。