miR-198 Represses the Proliferation of HaCaT Cells by Targeting Cyclin D2

miR-198 通过靶向细胞周期蛋白 D2 抑制 HaCaT 细胞增殖

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作者:Jian Wang, Guorong Dan, Tao Shangguan, Han Hao, Ran Tang, Kaige Peng, Jiqing Zhao, Huiqin Sun, Zhongmin Zou

Background

MiR-198 has been considered as an inhibitor of cell proliferation, invasion, migration and a promoter of apoptosis in most cancer cells, while its effect on non-cancer cells is poorly understood.

Conclusion

In conclusion, we have identified that miR-198 inhibited HaCaT cell proliferation by directly targeting CCND2.

Methods

The effect of miR-198 transfection on HaCaT cell proliferation was firstly detected using Cell Count Kit-8 and the cell cycle progression was analyzed by flow cytometry. Using bioinformatics analyses and luciferase assay, a new target of miR-198 was searched and identified. Then, the effect of the new target gene of miR-198 on cell proliferation and cell cycle was also detected.

Results

Here we showed that miR-198 directly bound to the 3'-UTR of CCND2 mRNA, which was a key regulator in cell cycle progression. Overexpressed miR-198 repressed CCND2 expression at mRNA and protein levels and subsequently led to cell proliferation inhibition and cell cycle arrest in the G1 phase. Transfection ofSiCCND2 in HaCaT cells showed similar inhibitory effects on cell proliferation and cell cycle progression.

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