Mir-186 inhibits the proliferation and growth of multiple myeloma cells by targeting Jagged-1 expression

被引:0
|
作者
Dong, Jinfeng [1 ,2 ]
Zheng, Xiaoqiang [1 ,2 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Dept Hematol, Fuzhou 350005, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Hematol, Binhai Campus, Fuzhou 350212, Fujian, Peoples R China
关键词
mir-186; Targeted regulation; Jagged1; Inhibition; Multiple myeloma; Multiplication; Growth; CISPLATIN SENSITIVITY; CANCER CELLS; METASTASIS; PROMOTES;
D O I
10.4314/tjpr.v23i1.1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To investigate the suppressive influence of mir -186 on multiplication and growth of multiple myeloma (MM), as well as the processes involved. Methods: The U266 cells were divided into control, mir -186 overexpression, and inhibition groups. The latter two were transfected with mir -186 agent and antagonist, respectively. Cell viability, colony formation potential, cell cycle ratio, and Jagged-1 mRNA and protein levels were measured using various assays. Results: Cell growth increased over time in all groups. However, mir -186 overexpression cells showed significantly decreased growth and colony formation capacity, relative to control, while the mir -186 inhibition cells showed significantly higher growth and colony formation capacity. The study revealed a higher proportion of G0/G1 stage cells and lower proportion of S-phase cells in mir -186 overexpression cells than in control cells. The opposite effect was seen in mir -186 inhibition cells. Jagged-1 protein and mRNA levels were significantly lower in mir -186 overexpression cells and higher in mir -186 inhibition cells than in control group. The Jagged-1 knockout group showed significantly higher Jagged-1 mRNA and protein levels than both the control and mir -186 overexpression groups (p < 0.05). Conclusion: When overexpressed, mir -186 inhibits the growth of multiple myeloma cells by inhibiting cell colony-formation capacity and by regulating cell cycle through mir-186-induced regulation of the expression of Jagged-1. there is need for more research to confirm the clinical benefits of therapies based on these findings.
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页码:1 / 6
页数:6
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