
Stem cell marker, Musashi-1 (MSI1) is over-expressed in many cancer types; however the molecular mechanisms involved in MSI1 over-expression are not well understood. We investigated the microRNA (miRNA) regulation of MSI1 and the implications this regulation plays in colorectal cancer. MicroRNA miR-137 was identified as a MSI1-targeting microRNA by immunoblotting and luciferase reporter assays. MSI1 protein was found to be highly expressed in 79% of primary rectal tumors (n=146), while miR-137 expression was decreased in 84% of the rectal tumor tissues (n=68) compared to paired normal mucosal samples. In addition to reduced MSI1 protein, exogenous expression of miR-137 inhibited cell growth, colony formation, and tumorsphere growth of colon cancer cells. Finally, in vivo studies demonstrated that induction of miR-137 can decrease growth of human colon cancer xenografts. Our results demonstrate that miR-137 acts as a tumor-suppressive miRNA in colorectal cancers and negatively regulates oncogenic MSI1.
570, Blotting, Western, Mice, Nude, RNA-binding proteins, Nerve Tissue Proteins, Real-Time Polymerase Chain Reaction, Mice, Animals, Humans, Genes, Tumor Suppressor, Rectal cancer, Tumor-initiating cells, RNA-Binding Proteins, HCT116 Cells, Immunohistochemistry, Colon cancer, Gene Expression Regulation, Neoplastic, MicroRNAs, Tissue Array Analysis, Disease Progression, Heterografts, Colorectal Neoplasms
570, Blotting, Western, Mice, Nude, RNA-binding proteins, Nerve Tissue Proteins, Real-Time Polymerase Chain Reaction, Mice, Animals, Humans, Genes, Tumor Suppressor, Rectal cancer, Tumor-initiating cells, RNA-Binding Proteins, HCT116 Cells, Immunohistochemistry, Colon cancer, Gene Expression Regulation, Neoplastic, MicroRNAs, Tissue Array Analysis, Disease Progression, Heterografts, Colorectal Neoplasms
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
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