05). These data obviously showed that upresgulation of miR-451 might effectively enhance the sensitivity of A549 cells to DDP. Figure 5 Effect of miR-451 upregulation on the in
vitro sensitivity of A549 cells to DDP. A. KPT-8602 ic50 Effects of various concentrations (0, 5, 10, 15, 20 and 25 μg/ml) of DDP on cells (mock A549, A549/miR-NC or A549/miR-451) for 12 h assessed by MTT assay. B. Effects of 5 μg/ml DDP on cells (mock A549, A549/miR-NC or A549/miR-451) for varied time length (0, 12, 24, 36 and 48 h) evaluated by MTT assays. C. Effects of 5 μg/ml DDP on colony formation of cells (mock A549, A549/miR-NC or A549/miR-451). All experiments were performed in triplicate, * P < 0.05. Upregulation of miR-451 enhances DDP-induced apoptosis of A549 cells The precise underlying mechanisms by which upregulation Silmitasertib concentration of miR-451 enhances chemosensitivity of A549 cells to DDP were further investigated. Then, the apoptosis was detected by flow cytometric assay. As shown in Figure 6A, the apoptotic rare of A549/miR-451 treated with 5 μg/ml DDP was increased by approximately 11.7% in comparison with mock A549 cells treated with 5 μg/ml DDP (P < 0.05). However, the apoptotic rate of A549/miR-NC cells treated with DDP showed no significant difference compared with that of mock A549 cells treated with DDP (P > 0.05). Figure 6B showed the results of AnnexinV-FITC apoptosis
detection assay, which HKI-272 concentration confirmed the results of flow cytomeric assay. Finally, the activity of caspase-3 was also determined by colorimetric assay.
As shown in Figure 6C, the caspase-3 activity in A549/miR-451 Carteolol HCl cells treated with DDP remarkably increased by approximately 308% compared that mock A549 or A549/miR-NC cells treated with DDP (P < 0.05). Therefore, upregulation of miR-451 might increase DDP chemosensitivity of A549 cells by enhancing DDP-induced apoptosis. Figure 6 Effect of combined miR-451 upregulation with DDP (5 μg/ml) on apoptosis of A549 cells. A. Flow cytometry analysis of apoptosis in mock A549, A549/miR-NC or A549/miR-451 cells. B. Hoechst staining analysis of apoptosis in mock A549, A549/miR-NC or A549/miR-451 cells. C. Analysis of relative caspase-3 activity in mock A549, A549/miR-NC or A549/miR-451 cells. All experiments were performed in triplicate. Upregulation of miR-451 increases in vivo chemosensitivity of A549 cells to DDP To explore whether upregulation of miR-451 on chemosensitivity of A549 cells to DDP in vivo, s.c. tumors were developed in nude mice followed by treatment with DDP or PBS. As shown in Figure 7A, the tumors formed from A549/miR-451cells grew significantly slower than those from A549/miR-NC after the treatment with DDP. At 28 days after inoculation, the average tumor volume of A549/miR-451 cells (212 ± 36 mm3) was significantly lower than that of A549/miR-NC (323 ± 13 mm3) following DDP treatment (P < 0.05; Figure 7B).