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. 2017 Jul 22;6(3):58. doi: 10.3390/antiox6030058

Figure 2.

Figure 2

Different types of DNA damage after a 1 h exposure to 5 mM AA, 6 Gy, 5 mM AA + 6 Gy and 500 μM H2O2. (A) Histograms of 8OH-dG lesions 48 h after treatments of LN18 cells. (B) Median fluorescence intensity (MFI) fold change compared with untreated cells of LN18, T98G, NZG0809 and NZG1003 cells. Values are averages ± SEM of at least 3 independent experiments in triplicate. Increased 8OH-dG lesions for H2O2 treatment over AA, Gy and AA + Gy was statistically significant (p < 0.05: unpaired two-tailed student t-test) for T98G and NZG1003. C. Representative photograph of comet tails (DSBs) of LN18 cells after a 1 h exposure to 5 mM AA. D. Fold change compared with controls of comet tail length of the different cell lines after a 1 h exposure to 5 mM AA, 6 Gy, 5 mM AA + 6 Gy compared to untreated controls (set at 1). Average number of comet tails measured per cell line: 278 (controls), 162 (AA), 220 (Gy) and 272 (AA + Gy).