<p>Control cells or compounds-treated cells were allowed to migrate towards lower insert chambers containing FBS as chemoattractant, for 22 hours. The morphology of cells in the different treatments migrating toward FBS is in the bottom panels. Positive control (C+) represents migrating cells without any treatment, negative control (C-) represents untreated cells migrating toward an FBS-free medium. Data represent mean ± SD of three independent assays in triplicate. The results were compared using ANOVA, followed by a Tukey's post-hoc analysis. Asterisks represent *<i>p</i>≤0.05, **<i>p</i>≤0.001 compared to control (C+).</p
<p>Cells were plated in culture plates fitted with 8-uM pore membranes to create upper and lower cel...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
<p>A2780 cells were treated with different concentration of WFA and CIS both alone and in combinatio...
<p><b>A</b>. Cells were scratched using a pipette tip to make gaps between cells before NGEN and NGE...
<p>Cells were plated in a 96-well plate and incubated with different concentrations (1 to 1000 µM) o...
<p><b>A</b>. Clonogenic assay of untreated MDA-MB-231 cells (control) or treated with NGEN or NGENCu...
<p><b>A</b>. Nuclear 4', 6-diamidino-2-phenylindole (DAPI) staining. Cells treated or not (control) ...
<p><b>A</b>. Zymography in 1% gelatin-SDS-PAGE. Lane 1: molecular mass marker (M); lane 2: control c...
<p>MDA-MB-231 cells were incubated or not (control) with 1 µM of NGEN or NGENCuB for 24 h. After, to...
<p>A431 cells were treated with different concentrations of naringenin (100 µM−300 µM) for 24 h, sta...
<p>Inhibition of tumour migration by a Boyden chamber assay. CaCo-2, HT29 and SW480 cells were plate...
<p>(A) Procyanidin A2, (B) procyanidin B1, and (C) morelloflavone. Inhibitors were used at 25 μM, 50...
<p>A) Schematic description of the Boyden chamber assay. RAW 264.7 cells were added to the upper cha...
<p><b>(A, B)</b> BT-549 cells and MDA—MB 231 were seeded in the Matrigel-coated upper compartment of...
<div><p>A) Boyden chamber assay evaluation of FBS induced cell migration of TCam-2 cells. Increasing...
<p>Cells were plated in culture plates fitted with 8-uM pore membranes to create upper and lower cel...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
<p>A2780 cells were treated with different concentration of WFA and CIS both alone and in combinatio...
<p><b>A</b>. Cells were scratched using a pipette tip to make gaps between cells before NGEN and NGE...
<p>Cells were plated in a 96-well plate and incubated with different concentrations (1 to 1000 µM) o...
<p><b>A</b>. Clonogenic assay of untreated MDA-MB-231 cells (control) or treated with NGEN or NGENCu...
<p><b>A</b>. Nuclear 4', 6-diamidino-2-phenylindole (DAPI) staining. Cells treated or not (control) ...
<p><b>A</b>. Zymography in 1% gelatin-SDS-PAGE. Lane 1: molecular mass marker (M); lane 2: control c...
<p>MDA-MB-231 cells were incubated or not (control) with 1 µM of NGEN or NGENCuB for 24 h. After, to...
<p>A431 cells were treated with different concentrations of naringenin (100 µM−300 µM) for 24 h, sta...
<p>Inhibition of tumour migration by a Boyden chamber assay. CaCo-2, HT29 and SW480 cells were plate...
<p>(A) Procyanidin A2, (B) procyanidin B1, and (C) morelloflavone. Inhibitors were used at 25 μM, 50...
<p>A) Schematic description of the Boyden chamber assay. RAW 264.7 cells were added to the upper cha...
<p><b>(A, B)</b> BT-549 cells and MDA—MB 231 were seeded in the Matrigel-coated upper compartment of...
<div><p>A) Boyden chamber assay evaluation of FBS induced cell migration of TCam-2 cells. Increasing...
<p>Cells were plated in culture plates fitted with 8-uM pore membranes to create upper and lower cel...
<p>Horizontal migration: (A-C) Vybrant CM-Dil labeled HSC-3 (red) and Vybrant DiO-labeled Mfs (green...
<p>A2780 cells were treated with different concentration of WFA and CIS both alone and in combinatio...