<p>(A) The indicated cell type were either untreated (control) or treated with 50 uM of ACCA and cell growth was assessed for 1, 2, 3, 6, and 10 days. The trypan blue exclusion test is used to determine the number of viable cells. Values represent number of cells x10<sup>5</sup>. (B) The indicated cell type either untreated or treated with different doses of ACCA were seeded in 96 wells, and a standard MTT viability test was performed 24h and 48h. postreatment as described in «materials and methods». Columns, mean±SD, n = 3.</p
<p>Proliferation was determined by an MTT assay (mean ± SD, n = 4) for genistein (GEN, square), fing...
<p>MDA-MB231 and HT29 cells were cultured for 3 days in control medium or hESCs-CM, and cells were a...
<p>(<b>A</b>) Morphology of control and treated breast cancer cells indicative of growth arrest phen...
<p>The indicated cell type either untreated (UNTR) or treated with 25 or 200 uM of ACCA were allowed...
<p>The indicated cell type either untreated (UNTR) or treated with 200 uM of ACCA for 48h. were stai...
a<p>C = control group.</p>b<p>Cells were analyzed by flow cytometry after being stained with Annexin...
<p>Lysates of the indicated cell type either untreated (UNTR) or treated with 200 uM of ACCA for 48h...
Cell proliferation was evaluated by MTS assay and expressed as percentage value with respect to cont...
This study investigated the underlying mechanism of 4-hydroxy-3-methoxycinnamic acid (ACCA), on the ...
<p>The mature adipocytes were indirectly co-cultured with various breast cancer cells for three days...
<p>A) Cell proliferation. Cells were counted every 24 hrs during treatment with 5-AZA. B) Cell viabi...
Using the primary cultured cells of cancerous thoracic fluid, cancerous ascites and mammary cancer t...
<p>Each point represents the mean (±SEM), <i>n</i> = 3 for each group. b) Cells response to gemcitab...
<p>Cells were treated for 24, 48 and 72 hours as indicated in the figures. Panels show: A) cell coun...
<p>(A) HeLa cells were treated with Am for 72 h as described in Material and Methods and cell viabil...
<p>Proliferation was determined by an MTT assay (mean ± SD, n = 4) for genistein (GEN, square), fing...
<p>MDA-MB231 and HT29 cells were cultured for 3 days in control medium or hESCs-CM, and cells were a...
<p>(<b>A</b>) Morphology of control and treated breast cancer cells indicative of growth arrest phen...
<p>The indicated cell type either untreated (UNTR) or treated with 25 or 200 uM of ACCA were allowed...
<p>The indicated cell type either untreated (UNTR) or treated with 200 uM of ACCA for 48h. were stai...
a<p>C = control group.</p>b<p>Cells were analyzed by flow cytometry after being stained with Annexin...
<p>Lysates of the indicated cell type either untreated (UNTR) or treated with 200 uM of ACCA for 48h...
Cell proliferation was evaluated by MTS assay and expressed as percentage value with respect to cont...
This study investigated the underlying mechanism of 4-hydroxy-3-methoxycinnamic acid (ACCA), on the ...
<p>The mature adipocytes were indirectly co-cultured with various breast cancer cells for three days...
<p>A) Cell proliferation. Cells were counted every 24 hrs during treatment with 5-AZA. B) Cell viabi...
Using the primary cultured cells of cancerous thoracic fluid, cancerous ascites and mammary cancer t...
<p>Each point represents the mean (±SEM), <i>n</i> = 3 for each group. b) Cells response to gemcitab...
<p>Cells were treated for 24, 48 and 72 hours as indicated in the figures. Panels show: A) cell coun...
<p>(A) HeLa cells were treated with Am for 72 h as described in Material and Methods and cell viabil...
<p>Proliferation was determined by an MTT assay (mean ± SD, n = 4) for genistein (GEN, square), fing...
<p>MDA-MB231 and HT29 cells were cultured for 3 days in control medium or hESCs-CM, and cells were a...
<p>(<b>A</b>) Morphology of control and treated breast cancer cells indicative of growth arrest phen...