To investigate the inhibitory effect and mechanism of resveratrol(Res)combined with oxaliplatin(Oxa)on the malignant biological behavior of human colon cancer cells.Methods:Colon cancer HCT-116 cells were cultured in vitro.The Res group, the Oxa group, the combination group and the control group were treated with 100 μmoL/L Res, 2 μmoL/L Oxa and 100 μmoL/L Res+2 μmoL/L Oxa, the same amount of saline, and each group was treated for 24, 36, 48 h.The inhibition of proliferation of colon cancer HCT-116 cells was detected by MTT assay; Transwell chamber assay was used to detect the invasion ability of colon cancer HCT-116 cells; Wound healing method was used to detect the migration ability of colon cancer HCT-116 cells; The expression of Vimentin protein(vimentin)in colon cancer HCT-116 cells was detected by Western blotting(Wb)method.Results:At 48 h after intervention, the proliferation inhibition rates of HCT-116 cells in the Res group, the Oxa group and the combination group were(28.41±6.25),(36.11±8.47)and(83.61±12.72)%, respectively; At 48 h after intervention, the invasive rates of HCT-116 cells in the control group, the Res group, the Oxa group and the combination group were(97.14±2.81),(81.23±4.52),(69.84±3.97),(37.11±3.58)%, respectively; The mobility rates were(68.57±4.02),(46.11±3.13),(31.25±2.86), and(18.79±2.21)%, respectively; The relative expression levels of Vimentin protein were(0.93±0.14),(0.52±0.08),(0.31±0.04), and(0.13±0.02), respectively.The proliferation inhibition rate of colon cancer HCT-116 cells in the Res group, the Oxa group and the combination group increased gradually(P<0.05); Compared with the control group, the invasion rate, mobility rate and Vimentin protein expression of HCT-116 cells in the Res group, the Oxa group and the combination group significantly decreased, and the combination group was significantly lower than the Res group and the Oxa group(all P<0.05).Conclusion:The combination of Res and Oxa has significant synergistic effect, which can inhibit the proliferation of colon cancer HCT-116 cells and reduce its invasion and migration rate, and its mechanism may be related to the down-regulation of Vimentin protein expression. |