Table 1. Bioinformatic pathway analysis of the most significantly up-regulated miRNAs from atherogenic EVs.
miRSystem (http://mirsystem.cgm.ntu.edu.tw/) was used and listed here are the most enriched pathways, including how many miRNAs (out of 10) are predicted to target the pathway. A gene is considered as a potential target of a miRNA using at least 3 prediction algorithms.
| Predicted pathways | Target Genes of Interest | # miRNAs targeting pathway (/10) |
|
|---|---|---|---|
| Pathways Predicted to be targeted by dysregulated miRNAs | Leukocyte Transendothelial Migration | PI3 kinase receptor 1, RhoA, ROCK1, ROCK2, PECAM, Cadherin 5, Cdc42, Protein kinase C-β | 7 |
| Cell Adhesion Molecules | PTEN, PI3 kinase R1, Cell adhesion molecule 1 (CADM1), Cadherin 5, VEGFA, Collagen 1α2, Collagen 4α6, CD34 | 6 | |
| Regulation of Actin Cytoskeleton | Fibronectin, FGF1, FGFR1, FGF12, Actinin alpha 1 (ACTN1), Actinin α4 (ACTN4), Integrin α3 | 7 | |
| Axon Guidance | DCC, UNC5C, Eph receptor A7 (EPHA7), Netrin G1, Semaphorin 3A, Semaphorin 6A, Eph receptor B2 (EPHB2), Eph receptor B1, ROBO1 | 7 | |
| Chemokine Signaling Pathway | CX3CL1, CXCL12, CXCL2, CXCR4, LYN, STAT5B, ELMO1 | 7 |