<p>LNCaP and PC-3 cells were treated with subditine (<b>1</b>) (12.5 µM, 25 µM, 50 µM) for 24 h. Cells were then fixed and stained with DHE dye. ROS levels were indirectly determined by measuring DHE dye incorporation in the nuclear using Cellomic HCS arrayscan. Increased DHE dye intensity in the nucleus was detected upon treatment of subditine. Hoechst (blue) and DHE dye (green). Bar chart showing the average fluorescent intensity of DHE stain (mean ± S.D.; *p<0.05).</p
<p>ROS level was determined by measuring the intensity of dihydroethidium (DHE) fluorescence. The re...
<p>Jurkat cells (1 × 10<sup>6</sup>/well) were exposed to DHA (0, 10, 20, 40, 80 μM) or DHA/HTF for ...
<p>(<b>A</b>) Cell viability (MTT assay) of MCF-7 cells treated with different concentrations of α-t...
<p>MCF-7 cells were pretreated with DESs for 24 h and stained with DHE dye to determine the ROS prod...
<p>(A) MCF-7 or MDA-MB-231 cells were treated with DMSO (control) or indicated concentration of vern...
<p>(A,B,E,F) VSMCs were stimulated as indicated for 30 min before labeling cells with DHE. Superoxid...
<p>LNCaP and PC-3 cells were treated with subditine (<b>1</b>) for 24 h. Cells were then fixed and s...
<p>Cells were treated with 40 µg/ml NB and/or 20 µM Cur at 37°C for different times after treatment ...
<p>(<b>A</b>) Cells were pre-treated with H(H<sub>2</sub>O)<sub>m</sub> for 15 min, then irradiated ...
<p>LNCaP and PC-3 cells were treated with subditine (<b>1</b>) (12.5 µM and 25 µM) for 24 h. Cells w...
<p>(A) PC12 cells were treated with DMSO or 50 nM TCDD for 72 h. The cells were then stained to exam...
<p>Cells were labeled with carboxy-H<sub>2</sub>DCFDA, which exhibits green fluorescence upon reacti...
<p><b>(A)</b> Each antioxidant scavenges ROS as a consequence of their chemical structures. Each als...
<p>Top panels (A) illustrate the results for A549 cancer cells while the bottom panels (B) depict th...
<p>ROS levels were evaluated by H<sub>2</sub>DCFDA staining after SsnB treatments (1 µM or 10 µM) fo...
<p>ROS level was determined by measuring the intensity of dihydroethidium (DHE) fluorescence. The re...
<p>Jurkat cells (1 × 10<sup>6</sup>/well) were exposed to DHA (0, 10, 20, 40, 80 μM) or DHA/HTF for ...
<p>(<b>A</b>) Cell viability (MTT assay) of MCF-7 cells treated with different concentrations of α-t...
<p>MCF-7 cells were pretreated with DESs for 24 h and stained with DHE dye to determine the ROS prod...
<p>(A) MCF-7 or MDA-MB-231 cells were treated with DMSO (control) or indicated concentration of vern...
<p>(A,B,E,F) VSMCs were stimulated as indicated for 30 min before labeling cells with DHE. Superoxid...
<p>LNCaP and PC-3 cells were treated with subditine (<b>1</b>) for 24 h. Cells were then fixed and s...
<p>Cells were treated with 40 µg/ml NB and/or 20 µM Cur at 37°C for different times after treatment ...
<p>(<b>A</b>) Cells were pre-treated with H(H<sub>2</sub>O)<sub>m</sub> for 15 min, then irradiated ...
<p>LNCaP and PC-3 cells were treated with subditine (<b>1</b>) (12.5 µM and 25 µM) for 24 h. Cells w...
<p>(A) PC12 cells were treated with DMSO or 50 nM TCDD for 72 h. The cells were then stained to exam...
<p>Cells were labeled with carboxy-H<sub>2</sub>DCFDA, which exhibits green fluorescence upon reacti...
<p><b>(A)</b> Each antioxidant scavenges ROS as a consequence of their chemical structures. Each als...
<p>Top panels (A) illustrate the results for A549 cancer cells while the bottom panels (B) depict th...
<p>ROS levels were evaluated by H<sub>2</sub>DCFDA staining after SsnB treatments (1 µM or 10 µM) fo...
<p>ROS level was determined by measuring the intensity of dihydroethidium (DHE) fluorescence. The re...
<p>Jurkat cells (1 × 10<sup>6</sup>/well) were exposed to DHA (0, 10, 20, 40, 80 μM) or DHA/HTF for ...
<p>(<b>A</b>) Cell viability (MTT assay) of MCF-7 cells treated with different concentrations of α-t...