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The epithelial-mesenchymal transition (EMT) contributes to cancer progression, as well as the development of normal organs, wound healing and organ fibrosis. We established a cell-based reporter system for identifying EMT-inducing microRNAs (miRNAs) with a gastric cancer (GC) cell line, MKN1, transfected with a reporter construct containing a promoter sequence of VIM in the 5′ upstream region of the TurboRFP reporter gene. Function-based screening using this reporter system was performed with adoi:10.1093/carcin/bgv106 pmid:26264654 fatcat:ykjx6iprfra7nmltj67iydy6hq