Correction: Drif et al. Anti-Inflammatory and Cancer-Preventive Potential of Chamomile (Matricaria chamomilla L.): A Comprehensive In Silico and In Vitro Study. Biomedicines 2024, 12, 1484

Abstract

There was an error in the original publication [...].

Figure 10

Detection of cell death in CCRF-CEM cells using flow cytometry and annexin-V/PI staining to measure apoptosis using a flow cytometer. (A,B) Cells treated with 0.25 × IC₅₀, 0.5 × IC₅₀, 1 × IC₅₀, 2 × IC₅₀, and 4 × IC₅₀ of quercetin and lupeol, for 72 h. DMSO was used as negative control. (A) Cells treated with lupeol and (B) cells treated with quercetin. Q1 represents necrotic cells (−) annexin V/(+) PI; Q2 represents late apoptotic cells exhibiting annexin V (+)/PI (+); Q3 represents early apoptotic cells (+) annexin V/(−) PI; Q4 represents viable cells (−) annexin V/(−) PI. (C,D) Bar diagrams representing the percentages of cells in the different quadrants. (C) Effects of lupeol and (D) Effects of quercetin. The treatment of both compounds at increasing concentrations significantly enhanced the percentage of necrotic cells. *** p < 0.001, ** p < 0.01, and * p < 0.05 compared to the negative control using paired two-tailed t-test. The bar diagrams were created based on the calculation of the mean values ± SD of three independent experiments.