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. Author manuscript; available in PMC: 2021 Dec 21.

Published in final edited form as: Anticancer Res. 2021 Dec;41(12):5919–5933. doi: 10.21873/anticanres.15411

Figure 2. — The effect of DATS on TNF-α induced MDA-MB-231 and MDA-MB-468 breast cancer cells. A wound-healing assay was used to examine the effect of diallyl trisulfide (DATS) on cell migration in TNF-α induced MDA-MB-231 and MDA-MB-468 breast cancer cells (A and C) at various time points (0, 12, and 24 h). Wound healing assay representative image and quantification of MDA-MB-231 and MDA-MB-468 cell migration with a magnification of 40X. (B and D) Wound width % was statistically analyzed. At least 3 independent experiments were performed with n=3. The data are presented as the mean±S.E.M. Statistically significant differences between control vs. treatments were evaluated by a one-way ANOVA, followed by Dunnett’s multiple comparison test with **p<0.01 and ***p<0.001.

Figure 2. — The effect of DATS on TNF-α induced MDA-MB-231 and MDA-MB-468 breast cancer cells. A wound-healing assay was used to examine the effect of diallyl trisulfide (DATS) on cell migration in TNF-α induced MDA-MB-231 and MDA-MB-468 breast cancer cells (A and C) at various time points (0, 12, and 24 h). Wound healing assay representative image and quantification of MDA-MB-231 and MDA-MB-468 cell migration with a magnification of 40X. (B and D) Wound width % was statistically analyzed. At least 3 independent experiments were performed with n=3. The data are presented as the mean±S.E.M. Statistically significant differences between control vs. treatments were evaluated by a one-way ANOVA, followed by Dunnett’s multiple comparison test with **p<0.01 and ***p<0.001.