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Opinion Review
Copyright: ©Author(s) 2026.
World J Diabetes. Oct 15, 2026; 17(10): 125822
Published online Oct 15, 2026. doi: 10.4239/wjd.125822
Table 1 The regulatory functions of non-coding RNA and epigenetic modifications
NcRNA/modification
Expression pattern
Target genes
Downstream signaling pathways
Mainly affects cell/tissue
Experimental model
miR-126Early-stage diabetes ↑ late-stage ↓Genes associated with the VEGF pathway, SPRED1, PIK3R2VEGF/PI3K-AKT/eNOS angiogenesis pathwayEndothelial cells, skeletal muscle cellsAnimal models of vascular injury
miR-155↑SOCS1, SHIP1NF-κBMacrophagesIn vitro and animal models of diabetes-related inflammation
miR-146a↓ or lacks functionalityIRAK1, TRAF6NF-κB negative feedback regulationMacrophagesIn vitro and animal models of diabetes-related inflammation
MALAT1Diabetic vascular damage ↑VEGF, inflammatory factorsceRNA, epigenetic regulationEndothelial cells, skeletal muscleIn vitro and animal models of diabetic microvascular disease
GAS5Abnormal expressionInflammation-related genesceRNACardiovascular tissueHuman clinical samples
circRNA-ceRNA network↑ or ↓Multiple miRNAsGenes involved in angiogenesis, inflammation and calcificationEndothelial cells, smooth muscle cellsHuman clinical samples
m6A modificationAbnormally ↑/↓MyoD mRNAMETTL3, FTOMyosatellite cellsHuman clinical samples
↑eNOS mRNAYTHDF2Endothelial cellsIn vitro high-glucose endothelial cell model
m6A-RBP networkAbnormal expressionInflammation, EMT-related mRNARBPsRenal tubules, blood vesselsHuman model of diabetic nephropathy


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