circRNA-miRNA-mRNA network in age-related macular degeneration: From construction to identification

被引:20
作者
Su, Yu [1 ]
Yi, Yuexiong [2 ]
Li, Lu [1 ]
Chen, Changzheng [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Ctr Eye, Wuhan 430060, Hubei, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Dept Obstet & Gynecol, Wuhan 430071, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Noncoding RNA; Age-related macular degeneration; Bioinformatics; Neurodegeneration disease; PROTEIN-INTERACTION NETWORKS; RETINAL-PIGMENT EPITHELIUM; OXIDATIVE STRESS; CIRCULAR RNAS; GENE-EXPRESSION; R PACKAGE; MICRORNAS; CERNA; NEOVASCULARIZATION; TARGET;
D O I
10.1016/j.exer.2020.108427
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The aim of the present study was to investigate the pathogenesis of age-related macular degeneration (AMD) by constructing a regulatory circRNA-miRNA-mRNA network. By adjusting the P value to 0.05 and the absolute log value of fold change to 0.25, 2920 and 1057 differentially expressed mRNAs were identified from GSE50195 and GSE29801, respectively. Based on a literature review, Starbase database analysis, and RNA hybrid assays, we obtained 77 miRNA-mRNA and 331 circRNA-miRNA pairs. After combining these pairs, we constructed a circRNA-miRNA-mRNA network possessing 303 circRNA nodes, 4 miRNA nodes, 51 mRNA nodes, and 408 edges. By utilizing protein-protein network analysis, the MCODE algorithm, and the highest degree of circRNA node, we identified the regulatory axis of hsa_circRNA7329/hsa-miR-9/SCD. Hsa_circRNA7329 may regulate SCD through hsa-miR-9 to promote macrophage-mediated inflammation and pathologic angiogenesis, which lead to AMD development. However, the underlying details require further investigation.
引用
收藏
页数:12
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