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(A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and <t>NucView</t> <t>488</t> <t>Caspase-3</t> substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.
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(A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and <t>NucView</t> <t>488</t> <t>Caspase-3</t> substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.
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(A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and <t>NucView</t> <t>488</t> <t>Caspase-3</t> substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.
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(A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and <t>NucView</t> <t>488</t> <t>Caspase-3</t> substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.
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Image Search Results


A significant activation of caspase-3/7 was observed after treating CEM cells for 5 h with compound 22 .

Journal: Frontiers in Pharmacology

Article Title: A novel quinine derivative as a PIM-1 kinase inhibitor induces apoptosis via mitochondrial depolarization with selective cytotoxicity in acute lymphoblastic leukemia cells

doi: 10.3389/fphar.2026.1799674

Figure Lengend Snippet: A significant activation of caspase-3/7 was observed after treating CEM cells for 5 h with compound 22 .

Article Snippet: Caspase-3/7 activation was assessed in CEM cells using the NucView 488 caspase-3 fluorogenic substrate (Biotium, #10402, Fremont, USA).

Techniques: Activation Assay

(A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and NucView 488 Caspase-3 substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.

Journal: bioRxiv

Article Title: Synergistic induction of a lethal Autosis-to-Apoptosis switch by Phytocannabinoids and beta-Caryophyllene in Triple-Negative Breast Cancer Cells

doi: 10.64898/2026.04.05.716056

Figure Lengend Snippet: (A) MDA-MB-231 cells were treated with vehicle (0.3% DMSO - Control) or combinations C1 to C3 as described in in the presence of SYTOX Green and SPY-DNA. Automated live-cell imaging was performed for 72h and representative composite images combining the phase contrast, green (SYTOX Green, dead cells), and NiR (SPY650-DNA, nuclei) fluorescence channels obtained at different time points are displayed. Dead cells (SPY + /SYTOX Green + nuclei) are indicated by white arrows. Insets show higher magnifications of specific elements. Blue boxes highlight retracted cells exhibiting cytoplasmic vacuoles, yellow boxes indicate cells displaying extensive cytoplasmic blebbing, and orange boxes highlight the formation of large cytoplasmic blisters (orange arrows) characteristic of secondary necrosis. Scale bar corresponds to 200 µm. See Videos S1-4 (Supplementary Material) for the complete 72 h time-lapse sequences. (B) MDA-MB-231 cells were treated with combinations C1 in the presence of SYTOX Orange and NucView 488 Caspase-3 substrate. Automated live-cell imaging was performed and representative phase contrast and composite images combining the green (NucView, active caspase-3) and orange (SYTOX Orange, dead cells) fluorescence channels obtained at different time points are displayed. Retracted cells are indicated by white arrow heads.

Article Snippet: To evaluate apoptosis, the NucView® 488 Caspase-3 enzyme substrate (0.5 μM; Biotium, USA) was used, with staurosporine (0.5 μM) as a specific positive control for caspase activation.

Techniques: Control, Live Cell Imaging, Fluorescence