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Impact of miR-192 and miR-194 on cyst enlargement through EMT in autosomal dominant polycystic kidney disease

Authors
Kim, Do YeonWoo, Yu MiLee, SunyoungOh, SuminShin, YubinShin, Jeong-OhPark, Eun YoungKo, Je YeongLee, Eun JiBok, JinwoongYoo, Kyung HyunPark, Jong Hoon
Issue Date
Feb-2019
Publisher
FEDERATION AMER SOC EXP BIOL
Keywords
ADPKD; DNA methylation; microRNA; ZEB2; N-cadherin
Citation
FASEB JOURNAL, v.33, no.2, pp 2870 - 2884
Pages
15
Journal Title
FASEB JOURNAL
Volume
33
Number
2
Start Page
2870
End Page
2884
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/3820
DOI
10.1096/fj.201800563RR
ISSN
0892-6638
1530-6860
Abstract
Altered miRNA (miR) expression occurs in various diseases. However, the therapeutic effect of miRNAs in autosomal dominant polycystic kidney disease (ADPKD) is unclear. Genome-wide analyses of miRNA expression and DNA methylation status were conducted to identify crucial miRNAs in end-stage ADPKD. miR-192 and -194 levels were down-regulated with hypermethylation at these loci, mainly in the intermediate and late stages, not in the early stage, of cystogenesis, suggesting their potential impact on cyst expansion. Cyst expansion has been strongly associated with endothelial-mesenchymal transition (EMT). Zinc finger E-box-binding homeobox-2 and cadherin-2, which are involved in EMT, were directly regulated by miR-192 and -194. The therapeutic effect of miR-192 and -194 in vivo and in vitro were assessed. Restoring these miRs by injection of precursors influenced the reduced size of cysts in Pkd1 conditional knockout mice. miR-192 and -194 may act as potential therapeutic targets to control the expansion and progression of cysts in patients with ADPKD.Kim, D. Y., Woo, Y. M., Lee, S., Oh, S., Shin, Y., Shin, J.-O., Park, E. Y., Ko, J. Y., Lee, E. J., Bok, J., Yoo, K. H., Park, J. H. Impact of miR-192 and miR-194 on cyst enlargement through EMT in autosomal dominant polycystic kidney disease.
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