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Fig. 3 | Journal of Experimental & Clinical Cancer Research

Fig. 3

From: CXCL12/CXCR4 promotes inflammation-driven colorectal cancer progression through activation of RhoA signaling by sponging miR-133a-3p

Fig. 3

CXCR4 enhanced CRC progression by inducing EMT and Wnt-β-catenin activation. a Representative H&E staining of colonic tissue with tumors from AOM/DSS treated WT and CXCR4+/− mice with or without AMD3100 treatment. b Representative images were shown to indicate the expression of E-cadherin, Vimentin, and active-β-catenin in different groups (n = 5) determined by immunohistochemistry assay (400 ×). Magnification of active β-catenin in black box was indicated and arrows pointed the nuclear staining of β-catenin. c Immunohistochemistry results were semi-quantified by image-pro plus 6 software and statistical analyses were performed (n = 5 for each group). *P < 0.05 vs. WT mice. #P < 0.05 vs. CXCR4+/− mice. d, e Levels of E-cadherin, vimentin, Snail, c-Myc, active-β-catenin/β-catenin, MMP7 normalized to β-actin were determined by Western blotting assay and statistical analyses were also performed

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