<p>Cell monolayers were scraped by a sterile micropipette tip and the cells were treated with various concentrations of diosgenin for 24 h. (A) Cells migrated to the wounded region were photographed (100× magnification). (B) The wound area of the cell cultures were quantified in four fields in each treatment, and data were calculated from three independent experiments. Data are presented as as mean ± S.D. of three independent experiments. <i>*p</i><0.05, <i>**p</i><0.01, compared with the untreated control.</p
A) Comparison of direct and automated cell counting of U87 cells maintained 48 h in culture in the p...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>Standard wounds were made with razor blades in confluent monolayers of IEC-6 cells as described i...
<p>Cells were treated with various concentrations of diosgenin for 24 h and cell invasion assay was ...
<p>Cells were treated with various concentrations of diosgenin for 24 h and 48 h. Cell viability is ...
<p>Wounds were made on monolayers of USPC-2 (A) and USPC-1 (B) cells grown to 100% confluence. Cells...
<p>A, Wound-healing assay showed that 5 μM DP did not affect movement of SW480 cells. Representative...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>(A) Representative phase-contrast images of the in vitro wound area in the different cell culture...
(a) Representative photomicrographs of PC-3M-1E8 cells and PC-3M-2B4 cells are presented at 200 × ma...
<p>UMR-106 monolayer were scraped with a pipette tip and incubated in the absence or presence of sim...
<p>(A) DMSO decreases cancer cell migration ability, as assessed by a scratch wound healing assay. T...
<p>Confluent MDA-MB-231 (A) and HS 578T (B) cells were scratched and incubated at different concentr...
<p>Cells were cultivated in 6-well plates at 4×10<sup>4</sup> cells/cm<sup>2</sup> until 100% conflu...
<p>(A) HUVECs were seeded onto Matrigel and incubated with conditioned medium from PC-3 cells treate...
A) Comparison of direct and automated cell counting of U87 cells maintained 48 h in culture in the p...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>Standard wounds were made with razor blades in confluent monolayers of IEC-6 cells as described i...
<p>Cells were treated with various concentrations of diosgenin for 24 h and cell invasion assay was ...
<p>Cells were treated with various concentrations of diosgenin for 24 h and 48 h. Cell viability is ...
<p>Wounds were made on monolayers of USPC-2 (A) and USPC-1 (B) cells grown to 100% confluence. Cells...
<p>A, Wound-healing assay showed that 5 μM DP did not affect movement of SW480 cells. Representative...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>(A) Representative phase-contrast images of the in vitro wound area in the different cell culture...
(a) Representative photomicrographs of PC-3M-1E8 cells and PC-3M-2B4 cells are presented at 200 × ma...
<p>UMR-106 monolayer were scraped with a pipette tip and incubated in the absence or presence of sim...
<p>(A) DMSO decreases cancer cell migration ability, as assessed by a scratch wound healing assay. T...
<p>Confluent MDA-MB-231 (A) and HS 578T (B) cells were scratched and incubated at different concentr...
<p>Cells were cultivated in 6-well plates at 4×10<sup>4</sup> cells/cm<sup>2</sup> until 100% conflu...
<p>(A) HUVECs were seeded onto Matrigel and incubated with conditioned medium from PC-3 cells treate...
A) Comparison of direct and automated cell counting of U87 cells maintained 48 h in culture in the p...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>Standard wounds were made with razor blades in confluent monolayers of IEC-6 cells as described i...