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Fig. 2 | Experimental Hematology & Oncology

Fig. 2

From: CUL4B-DDB1-COP1-mediated UTX downregulation promotes colorectal cancer progression

Fig. 2

Conditional deletion of Utx in intestinal epithelial cells increases susceptibility to AOM/DSS-induced colorectal tumorigenesis. A Schematic model of the AOM/DSS protocol used to induce colorectal tumors in C57BL/6 mice. i.p., intraperitoneal. B Relative body weight of WT and Utx−/x/Utx−/y was recorded during AOM/DSS treatment C and D Representative macroscopic (C) and H & E staining images (D) of large intestines from WT (n = 10), Utx−/x (n = 6), and Utx−/y (n = 5) mice at the end of the AOM/DSS protocol. Tumors were surrounded by dotted lines in representative images of H&E staining. Scale bar in (C), 5000 μm. Scale bar in (D), 1000 μm (left), and 20 μm (right), respectively. E and F Tumor number, tumor load (E), and size distribution of tumors (F) from large intestines of WT (n = 10), Utx−/x (n = 6), and Utx−/y (n = 5) mice. G Representative IHC images of Ki67 staining in large intestines of WT and Utx−/y mice post AOM/DSS-induced CRC tumorigenesis. Scale bar, 20 μm. Data information: In (B and E), data are presented as mean ± SEM (one-way ANOVA with Dunnett’s multiple comparisons test). In (F), data are presented as rates (chi-square test). ns, non-significance, *P < 0.05, **P < 0.01, ***P < 0.001

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