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EZH2 targeting induces oxidative stress without activating apoptotic pathways. ( A ) Relative mRNA expression levels of BAX, BCL2, and BAX/BCL2 ratio determined by RT-qPCR in A549 cells. Data are normalized to control and presented as mean ± SEM. Statistical significance was assessed relative to control (* p < 0.05, ** p < 0.01, *** p < 0.001). ( B ) Caspase-3 activity assay in A549 cells following treatment, with staurosporine as a positive control. Data are presented as percentage of positive control (mean ± SEM). ( C ) DCFH-DA assay <t>measuring</t> <t>intracellular</t> <t>ROS</t> levels in A549 cells following treatment with EPZ6438 and MS1943. Data are presented as percentage of control (mean ± SEM). Statistical significance was assessed relative to control (* p < 0.05, *** p < 0.001).
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EZH2 targeting induces oxidative stress without activating apoptotic pathways. ( A ) Relative mRNA expression levels of BAX, BCL2, and BAX/BCL2 ratio determined by RT-qPCR in A549 cells. Data are normalized to control and presented as mean ± SEM. Statistical significance was assessed relative to control (* p < 0.05, ** p < 0.01, *** p < 0.001). ( B ) Caspase-3 activity assay in A549 cells following treatment, with staurosporine as a positive control. Data are presented as percentage of positive control (mean ± SEM). ( C ) DCFH-DA assay <t>measuring</t> <t>intracellular</t> <t>ROS</t> levels in A549 cells following treatment with EPZ6438 and MS1943. Data are presented as percentage of control (mean ± SEM). Statistical significance was assessed relative to control (* p < 0.05, *** p < 0.001).
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EZH2 targeting induces oxidative stress without activating apoptotic pathways. ( A ) Relative mRNA expression levels of BAX, BCL2, and BAX/BCL2 ratio determined by RT-qPCR in A549 cells. Data are normalized to control and presented as mean ± SEM. Statistical significance was assessed relative to control (* p < 0.05, ** p < 0.01, *** p < 0.001). ( B ) Caspase-3 activity assay in A549 cells following treatment, with staurosporine as a positive control. Data are presented as percentage of positive control (mean ± SEM). ( C ) DCFH-DA assay measuring intracellular ROS levels in A549 cells following treatment with EPZ6438 and MS1943. Data are presented as percentage of control (mean ± SEM). Statistical significance was assessed relative to control (* p < 0.05, *** p < 0.001).

Journal: International Journal of Molecular Sciences

Article Title: EZH2 Regulates the Proliferation-Senescence Balance and Tumor–Stromal Signaling in Lung Adenocarcinoma

doi: 10.3390/ijms27135914

Figure Lengend Snippet: EZH2 targeting induces oxidative stress without activating apoptotic pathways. ( A ) Relative mRNA expression levels of BAX, BCL2, and BAX/BCL2 ratio determined by RT-qPCR in A549 cells. Data are normalized to control and presented as mean ± SEM. Statistical significance was assessed relative to control (* p < 0.05, ** p < 0.01, *** p < 0.001). ( B ) Caspase-3 activity assay in A549 cells following treatment, with staurosporine as a positive control. Data are presented as percentage of positive control (mean ± SEM). ( C ) DCFH-DA assay measuring intracellular ROS levels in A549 cells following treatment with EPZ6438 and MS1943. Data are presented as percentage of control (mean ± SEM). Statistical significance was assessed relative to control (* p < 0.05, *** p < 0.001).

Article Snippet: Intracellular ROS levels were measured using the ROS Assay Kit (MedChemExpress, Monmouth Junction, NJ, USA) based on the fluorescent probe DCFH-DA.

Techniques: Expressing, Quantitative RT-PCR, Control, Caspase-3 Activity Assay, Positive Control, DCFH-DA Assay