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Influence of in vitro digestion and food matrix on the genotoxicity of the Alternaria mycotoxin extract (15 μg/mL) in Caco-2 cells. Changes in the genotoxic properties of the CE were evaluated by applying the comet assay in the presence and absence of <t>formamidopyrimidine-DNA</t> <t>glycosylase</t> <t>(FPG).</t> Results are expressed as tail intensity (%) after 1 h of incubation. Exposure to UV-B radiation for 1 min served as the positive control. Dark and light blue bars indicate treatments without and with FPG, respectively. Statistical significance between non-FPG-treated samples and the solvent control (* p < 0.05, ** p < 0.01, *** p < 0.001), FPG-treated samples and the solvent control (#p < 0.05, ##p < 0.01, ###p < 0.001), and between treatments with and without FPG (within each sample; §p < 0.05, §§p < 0.01, §§§p < 0.001) was evaluated using Student's t -test. One-way ANOVA followed by Fisher's LSD post hoc test was used to evaluate differences across all conditions. Significant differences among FPG-treated samples are marked with lowercase letters, while capital letters denote differences among non-FPG-treated samples. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Formamidopyrimidine Dna Glycosylase Fpg Enzyme, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Influence of in vitro digestion and food matrix on the genotoxicity of the Alternaria mycotoxin extract (15 μg/mL) in Caco-2 cells. Changes in the genotoxic properties of the CE were evaluated by applying the comet assay in the presence and absence of <t>formamidopyrimidine-DNA</t> <t>glycosylase</t> <t>(FPG).</t> Results are expressed as tail intensity (%) after 1 h of incubation. Exposure to UV-B radiation for 1 min served as the positive control. Dark and light blue bars indicate treatments without and with FPG, respectively. Statistical significance between non-FPG-treated samples and the solvent control (* p < 0.05, ** p < 0.01, *** p < 0.001), FPG-treated samples and the solvent control (#p < 0.05, ##p < 0.01, ###p < 0.001), and between treatments with and without FPG (within each sample; §p < 0.05, §§p < 0.01, §§§p < 0.001) was evaluated using Student's t -test. One-way ANOVA followed by Fisher's LSD post hoc test was used to evaluate differences across all conditions. Significant differences among FPG-treated samples are marked with lowercase letters, while capital letters denote differences among non-FPG-treated samples. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
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Influence of in vitro digestion and food matrix on the genotoxicity of the Alternaria mycotoxin extract (15 μg/mL) in Caco-2 cells. Changes in the genotoxic properties of the CE were evaluated by applying the comet assay in the presence and absence of formamidopyrimidine-DNA glycosylase (FPG). Results are expressed as tail intensity (%) after 1 h of incubation. Exposure to UV-B radiation for 1 min served as the positive control. Dark and light blue bars indicate treatments without and with FPG, respectively. Statistical significance between non-FPG-treated samples and the solvent control (* p < 0.05, ** p < 0.01, *** p < 0.001), FPG-treated samples and the solvent control (#p < 0.05, ##p < 0.01, ###p < 0.001), and between treatments with and without FPG (within each sample; §p < 0.05, §§p < 0.01, §§§p < 0.001) was evaluated using Student's t -test. One-way ANOVA followed by Fisher's LSD post hoc test was used to evaluate differences across all conditions. Significant differences among FPG-treated samples are marked with lowercase letters, while capital letters denote differences among non-FPG-treated samples. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Journal: Food Chemistry: X

Article Title: Impact of in vitro digestion on the bioaccessibility, genotoxicity and mutagenicity of mycotoxins in a complex Alternaria extract

doi: 10.1016/j.fochx.2026.103481

Figure Lengend Snippet: Influence of in vitro digestion and food matrix on the genotoxicity of the Alternaria mycotoxin extract (15 μg/mL) in Caco-2 cells. Changes in the genotoxic properties of the CE were evaluated by applying the comet assay in the presence and absence of formamidopyrimidine-DNA glycosylase (FPG). Results are expressed as tail intensity (%) after 1 h of incubation. Exposure to UV-B radiation for 1 min served as the positive control. Dark and light blue bars indicate treatments without and with FPG, respectively. Statistical significance between non-FPG-treated samples and the solvent control (* p < 0.05, ** p < 0.01, *** p < 0.001), FPG-treated samples and the solvent control (#p < 0.05, ##p < 0.01, ###p < 0.001), and between treatments with and without FPG (within each sample; §p < 0.05, §§p < 0.01, §§§p < 0.001) was evaluated using Student's t -test. One-way ANOVA followed by Fisher's LSD post hoc test was used to evaluate differences across all conditions. Significant differences among FPG-treated samples are marked with lowercase letters, while capital letters denote differences among non-FPG-treated samples. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: Formamidopyrimidine DNA glycosylase (FPG) enzyme was supplied by New England Biolabs (Frankfurt, Germany), whereas dimethyl sulfoxide (DMSO) and ethidium bromide were purchased from Carl Roth GmbH + Co. KG (Karlsruhe, Germany).

Techniques: In Vitro, Single Cell Gel Electrophoresis, Incubation, Positive Control, Solvent, Control