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. 2018 Aug 30;9(9):895. doi: 10.1038/s41419-018-0924-z

Fig. 6. Encapsulated mirin reduces tumor growth and induces DDR and apoptosis in vivo.

Fig. 6

a Nude mice were subcutaneously inoculated with LAN5 cells. Mice were randomized and injected with 50 mg/kg of mirine or vehicle (empty nanoparticles) according to the indicated schedule (arrowheads), for a total of 1.25 mg of mirine/mouse. Tumor growth was monitored with the caliper every other day. Data represent the fold increase of the mean tumor volume compared to day 0, for each treatment group (n = 5) ±SEM. b Representative images of xenografted mice at day 11, before tumor explant. c Graph represents the mean volume of the excised tumors ±SEM. p was calculated by the Student’s t-test. *p < 0.05. d Histology, TUNEL assay, and immunostaining for γH2AX and p53S15P performed on tissue sections from tumor xenografts. Scale bar, 50 μm. e WB showing the expression level of the indicated proteins and phosphoepitopes in two representative tumors excised from mirine- or vehicle-treated mice