<p>Cells were exposed either to increasing concentrations of AMJ, or AMJ-derived fractions (tested at 21.4 µg/mL, equivalent to the polyphenol content of AMJ 0.3% v/v), or various isolated pure products (100 µM) for 24 h. (A), (B) and (C) cell apoptosis rates were assessed by flow cytometry using the annexin V-FITC/PI apoptosis assay. (D) The expression level of key regulators of cell cycle and apoptosis was assessed by Western blot analysis. The data are representative of at least three independent experiments. Values are shown as means ± S.E.M. (n = 3); *, <i>P<0.05</i> versus respective control.</p
<p>MOLM-13 or MV4;11 cells were seeded at an initial concentration of 1×10<sup>5</sup> cell mL<sup>−...
<p><b>A</b>. Flow cytometry profile represents Annexin V-FITC staining on the X-axis and PI staining...
<p>Assessment of apoptosis in (A) MDA-MB-231 and (C) HCT-8 cell lines treated with the extracts of M...
<p>(A) Pro-apoptotic effect of AMJ was assessed on various human leukemia cells (HSB-2, Molt-4 and C...
<p>Cells were exposed to increasing concentrations of AMJ for 24 h. (A) and (B) The formation of ROS...
<p>Cells were preincubated with Z-VAD-fmk, a pan-caspase inhibitor, before AMF treatment and apoptos...
<p>After incubation with AMF for the indicated time periods Annexin-V and propidiumiodide staining w...
<p>(A) Cytofluorimetric evaluation of apoptosis; representative Annexin V <i>versus</i> PI dot plot ...
<p>The indicated cell lines were incubated with (A) Nutlin-3a (0, 0.5, 1.0, 2.5, 5, or 10 μM), Ara-C...
<p>After incubation with AMF for the indicated time periods Annexin-V and propidiumiodide staining w...
<p>Cells were treated by APRTP-Js for 240 s, 480 s and 720 s, and then cultured for 24 h. (A) Cells ...
<p>A375 cells were treated with the indicated concentrations of compound <b>1</b> (0.03 to 3 μM) or ...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
<p>Cells were pretreated in the presence or absence of the specific inhibitors of caspase-9 (Z-LEHD-...
<p>MOLM-13 or MV4;11 cells were seeded at an initial concentration of 1×10<sup>5</sup> cell mL<sup>−...
<p><b>A</b>. Flow cytometry profile represents Annexin V-FITC staining on the X-axis and PI staining...
<p>Assessment of apoptosis in (A) MDA-MB-231 and (C) HCT-8 cell lines treated with the extracts of M...
<p>(A) Pro-apoptotic effect of AMJ was assessed on various human leukemia cells (HSB-2, Molt-4 and C...
<p>Cells were exposed to increasing concentrations of AMJ for 24 h. (A) and (B) The formation of ROS...
<p>Cells were preincubated with Z-VAD-fmk, a pan-caspase inhibitor, before AMF treatment and apoptos...
<p>After incubation with AMF for the indicated time periods Annexin-V and propidiumiodide staining w...
<p>(A) Cytofluorimetric evaluation of apoptosis; representative Annexin V <i>versus</i> PI dot plot ...
<p>The indicated cell lines were incubated with (A) Nutlin-3a (0, 0.5, 1.0, 2.5, 5, or 10 μM), Ara-C...
<p>After incubation with AMF for the indicated time periods Annexin-V and propidiumiodide staining w...
<p>Cells were treated by APRTP-Js for 240 s, 480 s and 720 s, and then cultured for 24 h. (A) Cells ...
<p>A375 cells were treated with the indicated concentrations of compound <b>1</b> (0.03 to 3 μM) or ...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
<p>Cells were pretreated in the presence or absence of the specific inhibitors of caspase-9 (Z-LEHD-...
<p>MOLM-13 or MV4;11 cells were seeded at an initial concentration of 1×10<sup>5</sup> cell mL<sup>−...
<p><b>A</b>. Flow cytometry profile represents Annexin V-FITC staining on the X-axis and PI staining...
<p>Assessment of apoptosis in (A) MDA-MB-231 and (C) HCT-8 cell lines treated with the extracts of M...