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AIM: To investigate the underlying molecular mechanisms of miR-451 to inhibit proliferation of esophageal carcinoma cell line EC9706.METHODS: Assays for cell growth, apoptosis and invasion were used to evaluate the effects of miR-451 expression on EC cells. Luciferase reporter and Western blot assays were used to test whether cyclin-dependent kinase inhibitor 2D(CDKN2D) and MAP3K1 act as major targets of miR-451.RESULTS: The results showed that CDKN2 D and MAP3K1 are direct targets of miR-451. CDKN2 D and MAP3K1 overexpression reversed the effect of miR-451.MiR-451 inhibited the proliferation of EC9706 by targeting CDKN2 D and MAP3K1.CONCLUSION: These findings suggest that miR-451 might be a novel prognostic biomarker and a potential target for the treatment of esophageal squamous cell carcinoma in the future.
AIM: To investigate the underlying molecular mechanisms of miR-451 to inhibit proliferation of esophageal carcinoma cell line EC9706.METHODS: Assays for cell growth, apoptosis and invasion were used to evaluate the effects of miR-451 expression on EC cells. Luciferase reporter and Western blot assays were used to test whether cyclin-dependent kinase inhibitor 2D (CDKN2D) and MAP3K1 act as major targets of miR-451.RESULTS: The results showed that CDKN2 D and MAP3K1 are direct targets of miR- 451. CDKN2 D and MAP3K1 MiR-451 inhibited the proliferation of EC9706 by targeting CDKN2 D and MAP3K1.CONCLUSION: These findings suggest that miR-451 might be a novel prognostic biomarker and a potential target for the treatment of esophageal squamous cells carcinoma in the future.