Fig. 2From: Advanced assessment of migration and invasion of cancer cells in response to mifepristone therapy using double fluorescence cytochemical labelingMifepristone attenuates migration and invasion of cancer cells of the ovary (a, e), breast (b, f), prostate (c, g), or glia (d, h) through filter-based assays assessed by phase contrast microscopy. Cells were exposed to either vehicle of cytostatic concentrations of MF specific to each cell line for 72 h and then seeded into Boyden chambers. At various time-points (9, 18, and 24 h) cells that migrated through the insert were counted after staining with crystal violet. Data shown represent the mean ± s.e.m. of three independent experiments completed in triplicate (a-d). Vehicle (closed bars) and MF (open bars). Images at the right of panel A show inserts of SKOV-3 cells treated with vehicle or MF, 24 h following migration; white arrows: cells that migrated through the pores and re-attached to the other side of the membrane; yellow arrowheads: 8 μm membrane pores. Scale bars = 50 μm. *P < 0.05, **P < 0.01and ***P < 0.001 compared against vehicle. Statistical analysis was done using a two-way ANOVA followed by Bonferroni’s multiple-comparison test. For the invasion assays, data shown represent the mean ± s.e.m. of three independent experiments completed in triplicate. Vehicle (closed bars); MF (open bars)Back to article page