fig3

Novel <i>N</i>-chloroacetyl-2-pyrazoline analogs with 2-naphthyl and ferrocenyl groups: targeting histamine receptor H1 to overcome colorectal cancer drug resistance

Figure 3. Clac10 (5c) and Clac12 (5e) trigger apoptosis. (A) HCT116 and DLD1 cells were treated with the IC50 concentration of Clac10 (5c) and Clac12 (5e) for 48 h, stained with Annexin V (FITC) and PI, and analyzed by flow cytometry; (B) Quantification shows that both compounds significantly induced late apoptosis in HCT116 and DLD1 cells; (C) Lysates from HCT116 and DLD1 cells treated with Clac10 (5c) and Clac12 (5e) showed reduced levels of anti-apoptotic marker proteins BCL-XL, MCL-1, and BCL-2 compared to untreated controls. Data is presented as mean ± SD. An ordinary two-way ANOVA was used for statistical comparison. IC50: Half maximal inhibitory concentration; FITC: fluorescein isothiocyanate; PI: propidium iodide; BCL-XL: B-cell lymphoma-extra large; MCL-1: myeloid cell leukemia 1; BCL-2: B-cell lymphoma 2; SD: standard deviation; ANOVA: analysis of variance; BAX: BCL2-associated X protein.

Cancer Drug Resistance
ISSN 2578-532X (Online)

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