<p>Cells were treated with (A) 0.1% vehicle DMSO (control) for 48 h and annomuricin E at the IC<sub>50</sub> concentration for (B) 12, (C) 24 and (D) 48 h. After staining the cells with PI, the DNA contents were monitored using flow cytometry. (E) The representative bar chart shows the significant induction of G<sub>1</sub> cell cycle arrest by annomuricin E after 12 h of treatment. The data represent the means ± SEM of three independent experiments. *<i>P</i><0.05 compared with the control.</p
<p>(A) (left panel) Cell cycle distribution was determined by flow cytometry, on Mel-Juso, SK-Mel-2 ...
<p><b>A.</b> DNA content, analyzed by flow cytometry, 24 h after treatment with different concentrat...
<p>(A) Inhibition of MCF-7 (▪), HeLa (▴), EMT-6/AR1 (•) and MDA-MB-231(▾) cell proliferation by ansa...
<p>Cells were treated with the IC<sub>50</sub> concentration of annomuricin E for 3, 6, 12, 24 and 4...
<p>After 12 h of treatment with annomuricin E at the IC<sub>50</sub> concentration, the total nuclea...
<p>Cells were exposed to 0.1% vehicle DMSO (control) and annomuricin E at different concentrations f...
<p>The treated cells were stained with different and specific dyes for the detection of total nuclea...
<p>The cytotoxic effect of each fraction was examined against HT-29 cells for 48 h using an MTT assa...
<p>MCF-7 cells were treated with Mitocur-1 (5 and 10 µM) for a period of 24 h. (<b>A</b>) shows the ...
<p>HCT116 and p53KO cells were incubated in 15 μM IGG, 30 μM IGG or vehicle control for either 8 or ...
<p>Cells were treated with 0, 3.8, 7.5, or 15 µM DIM for 48 hr, then fixed in ice-cold 70% EtOH and ...
<p>The housekeeping gene β-actin was used for the normalization of the mRNA expression. The result d...
<p><b>A</b> Cell cycle analysis of U87MG cells was performed 24 h, 48 h and 72 h after CAP treatment...
<p>A, HUVECs were starved for 24 h, and then were treated with or without DHC (3–10 µM) for 18 hr. A...
<p>(A) NTUB1 and T24 cells were treated with 2-ME (2 µM) or DMSO (as non-treated control) for 24 h, ...
<p>(A) (left panel) Cell cycle distribution was determined by flow cytometry, on Mel-Juso, SK-Mel-2 ...
<p><b>A.</b> DNA content, analyzed by flow cytometry, 24 h after treatment with different concentrat...
<p>(A) Inhibition of MCF-7 (▪), HeLa (▴), EMT-6/AR1 (•) and MDA-MB-231(▾) cell proliferation by ansa...
<p>Cells were treated with the IC<sub>50</sub> concentration of annomuricin E for 3, 6, 12, 24 and 4...
<p>After 12 h of treatment with annomuricin E at the IC<sub>50</sub> concentration, the total nuclea...
<p>Cells were exposed to 0.1% vehicle DMSO (control) and annomuricin E at different concentrations f...
<p>The treated cells were stained with different and specific dyes for the detection of total nuclea...
<p>The cytotoxic effect of each fraction was examined against HT-29 cells for 48 h using an MTT assa...
<p>MCF-7 cells were treated with Mitocur-1 (5 and 10 µM) for a period of 24 h. (<b>A</b>) shows the ...
<p>HCT116 and p53KO cells were incubated in 15 μM IGG, 30 μM IGG or vehicle control for either 8 or ...
<p>Cells were treated with 0, 3.8, 7.5, or 15 µM DIM for 48 hr, then fixed in ice-cold 70% EtOH and ...
<p>The housekeeping gene β-actin was used for the normalization of the mRNA expression. The result d...
<p><b>A</b> Cell cycle analysis of U87MG cells was performed 24 h, 48 h and 72 h after CAP treatment...
<p>A, HUVECs were starved for 24 h, and then were treated with or without DHC (3–10 µM) for 18 hr. A...
<p>(A) NTUB1 and T24 cells were treated with 2-ME (2 µM) or DMSO (as non-treated control) for 24 h, ...
<p>(A) (left panel) Cell cycle distribution was determined by flow cytometry, on Mel-Juso, SK-Mel-2 ...
<p><b>A.</b> DNA content, analyzed by flow cytometry, 24 h after treatment with different concentrat...
<p>(A) Inhibition of MCF-7 (▪), HeLa (▴), EMT-6/AR1 (•) and MDA-MB-231(▾) cell proliferation by ansa...