作者: Chun-Hua Zhao , Le Qu , Hui Zhang , Rui Qu
DOI: 10.1097/MD.0000000000018042
关键词: Carcinogenesis 、 Gene 、 Breast cancer 、 Genome 、 KEGG 、 microRNA 、 Computational biology 、 Competing endogenous RNA 、 Medicine 、 Microarray
摘要: Background An increasing number of studies indicate that circular RNAs (circRNAs) participate in tumorigenesis. The aim this study was to elucidate the regulatory mechanisms circRNAs breast cancer based on construction circRNA-related ceRNA network. Methods expression profiles circRNAs, miRNAs, and mRNAs were obtained from Gene Expression Omnibus (GEO) Cancer Genome Atlas (TCGA) databases. A network constructed by Cytoscape. interactions among proteins analyzed using STRING database, hub genes extracted cytoHubba application. functions differentially expressed (DEmRNAs) Kyoto Encyclopedia Genomes (KEGG) Ontology (GO) database. Results In total, 7 (DEcircRNAs), 27 miRNAs (DEmiRNAs), 102 DEmRNAs selected for cancer. We established a protein-protein interaction identified 6 genes. Then, circRNA-miRNA-hub gene module 2 DEcircRNAs, DEmiRNAs, DEmRNAs. GO KEGG pathway analyses indicated possible association with onset progression. Conclusions circRNA hsa_circ_0000519 is likely critical pathogenesis may serve as future therapeutic biomarker.