RBBP4 promotes colon cancer malignant progressionviaregulating Wnt/β-catenin pathway

BACKGROUND Our previous study demonstrated that RBBP4 was upregulated in colon cancer and correlated with poor prognosis of colon cancer and hepatic metastasis. However, the potential biological function of RBBP4 in colon cancer is still unknown. AIM To investigate the biological role and the potential mechanisms of RBBP4 in colon cancer progression. METHODS Real-time polymerase chain reaction and western blot analysis were used to detect the expression of RBBP4 in colon cancer cell lines. The cell proliferation and viability of SW620 and HCT116 cells with RBBP4 knockdown was detected by Cell Counting Kit-8 and 5-ethynyl-2'-deoxyuridine staining. The transwell assay was used to detect the invasion and migration capabilities of colon cancer cells with RBBP4 knockdown. Flow cytometry apoptosis assay was used to detect the apoptosis of colon cancer cells. Western blotting analysis was used to detect the expression of epithelial-mesenchymal transition and apoptosis related markers in colon cancer. The nuclear translocation of beta-catenin was examined by Western blotting analysis in colon cancer cells with RBBP4 knockdown. The TOPFlash luciferase assay was used to detect the effect of RBBP4 on Wnt/beta-catenin activation. The rescue experiments were performed in colon cancer cells treated with Wnt/beta-catenin activator LiCl and RBBP4 knockdown. RESULTS We found that RBBP4 was highly expressed in colon cancer cell lines. The 5-ethynyl-2'-deoxyuridine assay showed that knockdown of RBBP4 significantly inhibited cell proliferation. RBBP4 inhibition reduced cell invasion and migrationviaregulating proteins related to epithelial-mesenchymal transition. Knockdown of RBBP4 significantly inhibited survivin-mediated apoptosis. Mechanistically, the TOPFlash assay showed that RBBP4 knockdown increased activity of the Wnt/beta-catenin pathway. Meanwhile, RBBP4 knockdown suppressed nuclear translocation of beta-catenin. With Wnt/beta-catenin activator, rescue experiments suggested that the role of RBBP4 in colon cancer progression was dependent on Wnt/beta-catenin pathway. CONCLUSION RBBP4 promotes colon cancer developmentviaincreasing activity of the Wnt/beta-catenin pathway. RBBP4 may serve as a novel therapeutic target in colon cancer.