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Chinese Journal of Cell and Stem Cell(Electronic Edition) ›› 2023, Vol. 13 ›› Issue (02): 76-83. doi: 10.3877/cma.j.issn.2095-1221.2023.02.002

• Original Research • Previous Articles     Next Articles

Effects of miR-127-3p targeting macrophage migration inhibitory factor on the biological behavior of human renal cancer cells

Xiaomei Liu, Lu Zhang, Xu Liu, Die Liang()   

  1. Tumor Center, Suining Central Hospital, Suining 629000, China
    Urology Surgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu 610072, China
  • Received:2022-04-07 Online:2023-04-01 Published:2023-08-04
  • Contact: Die Liang

Abstract:

Objective

To study the regulation of miR-127-3p on macrophage migration inhibitory factor (MIF) and its effect on the biological behavior of human renal cell carcinoma cell line GRC-1.

Methods

Human GRC-1 cells were transfected with miR-127-3p minic, MIF-overexpressed plasmid and cotransfected with miR-127-3p minic and MIF-overexpressed plasmid. The untreated cells were set as control. Real-time quantitative PCR was used to detect the expression of miR-127-3p and MIF mRNA in clinical renal cancer tissues and adjacent normal tissues, and the correlation between miR-127-3p and MIF mRNA expression levels in cancer tissues was analyzed by Pearson correlation. The luciferase reporter system determines the regulatory effect of miR-127-3p on MIF. The effects of miR-127-3p on cell proliferation, apoptosis, invasion and migration were analyzed, and the expression of MIF protein was detected. The measurement data between the two groups were compared by paired t-test, and the comparison between multiple groups was conducted by one-way ANOVA.

Results

Compared with adjacent tissues, the expression of miR-127-3p was decreased in renal cancer tissue (1.16 ± 0.25 vs 1.65 ± 0.38), while the expression of MIF mRNA was significantly increased (1.32 ± 0.18 vs 0.32 ± 0.11, P < 0.05). The expression levels of miR-127-3p and MIF mRNA in renal cancer tissues were negatively correlated (r = - 0.612, P < 0.05). Luciferase experiments showed that miR-127-3p targeted MIF. Compared with the control, the MIF overexpression increased cell proliferation after transfection 2 ~ 4 days, while the miR-127-3p mimic decreased cell proliferation (P < 0.05). Compared with the control, the apoptosis rate was increased in the miR-127-3p mimic-transfected cells and co-transfected GRC-1 cells. In contrast, the apoptosis rate was decreased in the MIF-overexpressed cells. Compared with the control, the miR-127-3p mimic decreased the invasion number and MIF protein expression in renal cancer GRC-1 cells, while MIF overexpression, and co-transfection increased the cell invasion number (P < 0.05). Compared with the control, the scratch healing rate was decreased in the miR-127-3p mimic -transfected cells and co-transfected cells. While the scratch healing rate was increased in the MIF-overexpressed cells (P < 0.05) .

Conclusion

miR-127-3p is underexpressed in renal cancer tissues, and miR-127-3p overexpression inhibits the proliferation, migration and invasion and induces apoptosis of renal cancer GRC-1 cells by down-regulating the expression of MIF.

Key words: miR-127-3p, Macrophage migration inhibitory factor, Renal cancer cell, Biological behavior, Molecular mechanism

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