miR-363 induces transdifferentiation of human kidney tubular cells to mesenchymal phenotype

Background microRNAs (miRNAs) are non-coding small RNAs that regulate embryonic development, cell differentiation and pathological processes via interaction with mRNA. Epithelial–mesenchymal transition (EMT) is pathological process that involves in a variety of diseases such as cancer or fibrosis. M...

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Veröffentlicht in:Clinical and experimental nephrology 2016-06, Vol.20 (3), p.394-401
Hauptverfasser: Morizane, Ryuji, Fujii, Shizuka, Monkawa, Toshiaki, Hiratsuka, Ken, Yamaguchi, Shintaro, Homma, Koichiro, Itoh, Hiroshi
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Sprache:eng
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Zusammenfassung:Background microRNAs (miRNAs) are non-coding small RNAs that regulate embryonic development, cell differentiation and pathological processes via interaction with mRNA. Epithelial–mesenchymal transition (EMT) is pathological process that involves in a variety of diseases such as cancer or fibrosis. Methods In this study, we identified miR-363 as a potent inducer of EMT by microarray analysis in human kidney tubular cells, and analyzed the function and mechanisms of miR-363. Results Overexpression of miR-363 induced mesenchymal phenotypes with loss of epithelial phenotypes in human kidney tubular cells. In addition, in vitro scratch assay demonstrated that miR-363 promotes cell migration of primary culture of human kidney tubular cells. We identified TWIST/canonical WNT pathway as the downstream effecter of miR-363, and inhibition of canonical WNT by small molecule, IWR-1, attenuated EMT induced by miR-363. Conclusion miR-363 induces transdifferentiation of human kidney tubular cells via upregulation of TWIST/canonical WNT pathway.
ISSN:1342-1751
1437-7799
DOI:10.1007/s10157-015-1167-2