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Silencing of DNMT3B Promotes Tumor Radiosensitivity In Vivo
(A) Overall scheme of animal experiments. (B) Representative tumor samples from each group are shown. (C) Tumor volumes from each group were tracked for 18 days. (D) Tumor weights in each group. (E) Representative IHC staining of DNMT3B, p53, p21 and cleaved caspase-3 from tumor samples in each non-irradiated group (original magnification, ×200). (F) Conceptual diagram of our study. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.
