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. 2021 Sep 8;27:104. doi: 10.1186/s10020-021-00370-8

Fig. 3.

Fig. 3

RT-qPCR analysis of differentially-expressed miRNAs. The miRNA–mRNA regulation network associated with the PI3K/AKT and MAPK pathways were constructed using the Gephi software (A). RT-qPCR analysis of differentially-expressed miRNAs (miR-504, miR-935, miR-484, miR-301-5p) in the serum of normal glucose tolerance subjects and type 2 diabetic patients (B). Data are presented as box plots, where all fold changes were calculated between medians. The y-axis indicates the expression level of miRNAs on a log2 scale. *p < 0.05, **p < 0.01, NS, not significant. The binding sites of miR-504 and miR-935 in the 3'-UTR of MEK5 and MEF2C mRNA were predicted using miRNA target prediction algorithms