<p>Cells were treated with A398 (4, 6 and 8 µM) or etoposide (5 µM) for 1 h, 3 h or 6 h and stained with annexin V-alexa fluor 488 and PI or with TMRM. The rate of apoptosis (A) and the percentage of depolarized cells (B) were quantified by flow cytometry. (C) Decreased expression of Bcl-2 in HL- 60 lineage. Cells were treated with 6 µM of A398 for 1 h, 3 h, 6 h and 12 h. The bands were revealed on nitrocellulose membrane after staining with secondary antibody labeled with peroxidase. β-actin was used as a loading control. C: control. (D) Bar plot showing arbitrary unit (AU) obtained from densitometry measure displayed in (C). Data are expressed as mean ± SE of three independent experiments. *p<0.05, **p<0.01 and ***p<0.001 compared with th...
<p>Morphological changes in the nuclei (typical of apoptosis) of cultured U937 cells (A and B). U937...
<p>(A) Cytofluorimetric evaluation of apoptosis; representative Annexin V <i>versus</i> PI dot plot ...
<p>Cells were treated with increasing concentrations of the substances for 24 h and cell viability w...
<p>(A) U937 cells were treated with 1.4 µg/ml HF for 72 h. Detection of apoptotic cells after annexi...
(A) Induction of cell apoptosis by FD268 at the increasing concentrations for 48h. Apoptotic cells w...
<p>Flow cytometric analyses were performed to determine the percent of apoptotic cells induced by an...
<p>For how compound A398 induced apoptosis in the leukemic HL-60 cells through the activation of the...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>(A) Expression of FLAG-tagged Bcl-2 in NCI-H460 cells. Equal amounts of whole cell lysates from N...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>(A) K562 or HL-60 cells were left untreated or treated with various concentrations of lapatinib o...
<p>Unsynchronized (A) and synchronized (B) HeLa cells were treated with 0, 20, or 30 µM DhL for 24 o...
Cells were treated with increasing concentrations of FD268 for 24 h. Transcriptional levels of apopt...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Morphological changes in the nuclei (typical of apoptosis) of cultured U937 cells (A and B). U937...
<p>(A) Cytofluorimetric evaluation of apoptosis; representative Annexin V <i>versus</i> PI dot plot ...
<p>Cells were treated with increasing concentrations of the substances for 24 h and cell viability w...
<p>(A) U937 cells were treated with 1.4 µg/ml HF for 72 h. Detection of apoptotic cells after annexi...
(A) Induction of cell apoptosis by FD268 at the increasing concentrations for 48h. Apoptotic cells w...
<p>Flow cytometric analyses were performed to determine the percent of apoptotic cells induced by an...
<p>For how compound A398 induced apoptosis in the leukemic HL-60 cells through the activation of the...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>(A) Expression of FLAG-tagged Bcl-2 in NCI-H460 cells. Equal amounts of whole cell lysates from N...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>(A) K562 or HL-60 cells were left untreated or treated with various concentrations of lapatinib o...
<p>Unsynchronized (A) and synchronized (B) HeLa cells were treated with 0, 20, or 30 µM DhL for 24 o...
Cells were treated with increasing concentrations of FD268 for 24 h. Transcriptional levels of apopt...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Morphological changes in the nuclei (typical of apoptosis) of cultured U937 cells (A and B). U937...
<p>(A) Cytofluorimetric evaluation of apoptosis; representative Annexin V <i>versus</i> PI dot plot ...
<p>Cells were treated with increasing concentrations of the substances for 24 h and cell viability w...