Tianjin Medical Journal ›› 2026, Vol. 54 ›› Issue (4): 344-351.doi: 10.11958/20252647

• Cell and Molecular Biology • Previous Articles     Next Articles

The effect of miR-493-3p on high glucose-induced myocardial cell injury and apoptosis via the lncRNA CCAT2/TCF7L2 axis

SONG Jinping(), CUI Yanjie, WANG Changmin()   

  1. Clinical Laboratory Center, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, China
  • Received:2025-08-08 Revised:2025-12-15 Published:2026-04-15 Online:2026-04-14
  • Contact: E-mail:wcm224@126.com

Abstract:

Objective To investigate the impact of miR-493-3p on high glucose-induced cardiomyocyte injury and apoptosis by regulating long noncoding RNA (lncCCAT2)/transcription factor 7-like 2 (TCF7L2) axis. Methods Diabetic cardiomyopathy (DCM) cell model (AC16) was established in vitro with high glucose (HG, 55 mmol/L glucose). Experimental grouping:the control group, the HG group, the si-RNA negative control group, the si-CCAT2 group, the RNA mimics negative control group, the miR-493-3p-mimics group, the miR-493-3p-mimics +Lentivirus negative control group and the miR-493-3p-mimics +LV-CCAT2 group. Cell viability and apoptosis rate were detected by CCK8 assay and flow cytometry. The levels of lactate dehydrogenase (LDH) and aspartate aminotransferase (AST) in cell culture medium and superoxide dismutase (SOD) in cells were detected by the kit methods. Dual luciferase reporter gene assay was used to verify the targeting relationship between miR-493-3p and lncRNA CCAT2. The expression of miR-493-3p, lncRNA CCAT2, β?catenin, TCF7L2, Caspase-3 and CyclinD1 genes were detected by RT-PCR. Western blot assay was used to detect the expressions of β-catenin (nuclear), β-catenin (Cytoplasm), TCF7L2, Caspase-3 and CyclinD1 proteins. Results Compared with the control group, miR-493-3p, OD450 and SOD were decreased in the HG group, and levels of lncRNA CCAT2, LDH, AST, apoptosis rate, the expression levels of TCF7L2 mRNA and protein increased. Up-regulating miR-493-3p or knocking down the expression of lncRNA CCAT2 can antagonize the above changes (P<0.05). The double luciferase reporter gene experiment verified the relationship between miR-493-3p and CCAT2 and TCF7L2. Compared with the HG+miR-493-3p-mimics group, the TCF7L2, β-catenin (nuclear), downstream Caspase-3 and CyclinD1 mRNA and protein expression were increased in the HG+miR-493-3p-mimics+LV-CCAT2 group (P<0.05). Conclusion miR-493-3p can alleviate myocardial cell injury and apoptosis under high glucose condition by inhibiting lncRNA CCAT2 expression, and there is a competitive relationship between the two regulation of TCF7L2.

Key words: diabetic cardiomyopathies, myocytes, cardiac, transcription factor 7-like 2 protein, apoptosis, miR-493-3p, LncRNA CCAT2

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