Skip to main content
. 2020 Sep 26;9:25. doi: 10.1186/s40164-020-00182-2

Fig. 4.

Fig. 4

Upregulated miR-100 or downregulated mTOR inhibited cell proliferation and arrested the cell cycle in MCL cells. a CCK-8 assay detected the OD value of cell proliferation in Jeko-1 cells. b Cell proliferation of Jeko-1 cells in the LV-miR-100-up group (day 3 p = 0.0026; day 4 p < 0.0001; day 5 = 0.0002) and the LV-mTOR-RNAi group (day 2 p = 0.0062; day 3 p = 0.0002; day 4 = 0.0003; day 5 p < 0.0001) was lower than that in the control and NC groups. c CCK-8 assay detected the OD value of the cell proliferation in Mino cells. d The data demonstrated that the cell proliferation of Mino cells in the LV-miR-100-up group (day 1 p = 0.0424; day 2 p = 0.0447; day 3 p = 0.0005; day 4 p = 0.0001; day 5 p < 0.0001) and the LV-mTOR-RNAi group (day 2 p = 0.0261; day 3 p < 0.0001; day 4 p < 0.0001; day 5 p < 0.0001) was lower than that in the control and NC groups. e Flow cytometry analyzed the cell cycle of Jeko-1 cells. f The data showed that the G1 cell cycle rates of Jeko-1 cells in the LV-miR-100-up and LV-mTOR-RNAi groups were higher than those in the NC group and control group, and the Jeko-1 S cell cycle rate in the LV-miR-100-up and LV-mTOR-RNAi groups was lower than those in the NC group and control group (p < 0.0001). g Flow cytometry analyzed the cell cycle of Mino cells. h The data showed that the G1 cell cycle rates of Mino cells in the LV-miR-100-up and LV-mTOR-RNAi groups were higher than those in the NC group and control group, and the S cell cycle rates in the LV-miR-100-up and LV-mTOR-RNAi groups were lower than those in the NC group and control group (p < 0.0001)