Effects of resveratrol on proliferation and invasion of lung cancer 95D cells
Chen Haixia
2018, 45 (12):
705-710.
doi: 10.3760/cma.j.issn.1673-422X.2018.12.001
ObjectiveTo study the effects of resveratrol on the proliferation and invasion capacity of human lung adenocarcinoma 95D cells. MethodsHuman lung adenocarcinoma 95D cells were treated with 0, 10, 20, 40, 80 μmol/L resveratrol and treated with 0 μmol/L as the control group. The proliferation level of 95D cells was measured by methyl thiazolyl tetrazolium (MTT). Cell cycle and apoptosis were detected by flow cytometry. Cell adhesion rate was determined by in vitro adhesion test. Cell invasiveness was measured by Transwell chamber. The expressions of matrix metalloproteinase2 (MMP2) and tissue inhibitior of metalloproteinase2 (TIMP2) were determined by fluorescent immunocytochemistry. ResultsWhen the 95D cells were treated with resveratrol for 72 h, the cell proliferation rates in groups treated with 0, 10, 20, 40, 80 μmol/L resveratrol were 100%, (82.23±0.33)%, (62.45±0.27)%, (49.89±0.43)%, (45.11±0.35)% respectively, with a significant difference (F=87.830, P=0.002). The proliferation rates of 95D cells in the 10, 20, 40, 80 μmol/L resveratrol groups were significantly inhibited compared with the control group (P=0.017, P<0.001, P<0.001, P<0.001). When the 95D cells were treated for 48 h, the apoptosis rates of cells in each group were 0, (34.90±0.91)%, (41.33±0.13)%, (45.47±0.87)%, (59.46±0.59)% respectively, with a significant difference (F=21.032, P=0.002). The apoptosis rates of 95D cells in the 10, 20, 40, 80 μmol/L resveratrol groups were significantly increased compared with the control group (P=0.001, P<0.001, P<0.001, P<0.001). When the 95D cells were treated for 48 h, the S phase cell percentages in each group were (18.12±0.62)%, (38.33±0.62)%, (54.15±0.74)%, (44.85±0.82)%, (50.01±0.35)% respectively, with a significant difference (F=104.156, P=0.001). The S phase cell percentages in the 10, 20, 40, 80 μmol/L resveratrol groups were significantly higher compared with the control group (P=0.001, P<0.001, P<0.001, P<0.001). When the 95D cells were treated for 24 h, the cell adhesion rates in each group were 100%, (87.41±0.02)%, (84.32±0.03)%, (68.23±0.04)%, (63.01±0.02)% respectively, with a significant difference (F=13.760, P<0.001). The cell adhesion rates in the 20, 40, 80 μmol/L resveratrol groups were significantly inhibited compared with the control group (P=0.035, P<0.001, P<0.001), while the 10 μmol/L resveratrol group had no significant difference compared with the control group (P=0.058). When the 95D cells were treated for 24 h, the cell invasion rates in each group were 100%, (97.01±0.03)%, (74.89±0.07)%, (34.07±0.03)%, (14.65±0.02)% respectively, with a significant difference (F=39.382, P=0.001). The cell invasion rates in the 20, 40, 80 μmol/L groups were significantly inhibited compared with the control group (P=0.012, P<0.001, P<0.001), while the 10 μmol/L resveratrol group had no significant difference compared with the control group (P=0.881). When the 95D cells were treated for 48 h, MMP2 protein expression was decreased in the 20 mol/L group, while TIMP2 protein expression was increased compared with the control group. ConclusionResveratrol can inhibit the proliferation of human lung adenocarcinoma 95D cells and has effect of antitumor cell invasiveness, and its mechanism may involve twoway regulation of MMP2/TIMP2 expression.
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