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Erschienen in: Heart and Vessels 8/2019

08.02.2019 | Original Article

Linc00299/miR-490-3p/AURKA axis regulates cell growth and migration in atherosclerosis

verfasst von: Yong Liu, Yaqing Chen, Lili Tan, Hongmei Zhao, Nuan Xiao

Erschienen in: Heart and Vessels | Ausgabe 8/2019

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Abstract

Long non-coding RNA (lncRNA) plays a crucial role in regulating various cellular processes in atherosclerosis. The present study identified the regulation of Linc00299, via miR-490-3p targeting Aurora kinase A (AURKA), on migration and proliferation of endothelial cells and vascular smooth muscle cells (VSMCs) during atherosclerosis. The expression of RNAs was assessed by real-time PCR. The proliferation, apoptosis and migration were detected using MTT assay, Annexin V/PI staining and Transwell system, respectively. Bindings of Linc00299/miR-490-3p and subsequent miR-490-3p/AURKA were verified by luciferase and biotin pull-down assays. The protein expression of AURKA was detected by Western blotting. Expressions of Linc00299 and miR-490-3p were upregulated and downregulated in atherosclerosis patients, respectively. Both Linc00299 knockdown and miR-490-3p overexpression suppressed cell proliferation, increased apoptosis and inhibited migration of VSMCs and HUVECs. Linc00299 directly bound to miR-490-3p which targeted AURKA. The regulation of Linc00299 on expression of AURKA and proliferation and migration of VSMCs were dependent on miR-490-3p. Atherosclerosis-increased Linc00299 acts as a sponge of miR-490-3p to upregulate AURKA, and as a result increases proliferation and migration in VSMCs and HUVECs. Our study reveals an important effect of Linc00299/miR-490-3p/AURKA axis on regulating cell proliferation and migration in atherosclerosis.
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Metadaten
Titel
Linc00299/miR-490-3p/AURKA axis regulates cell growth and migration in atherosclerosis
verfasst von
Yong Liu
Yaqing Chen
Lili Tan
Hongmei Zhao
Nuan Xiao
Publikationsdatum
08.02.2019
Verlag
Springer Japan
Erschienen in
Heart and Vessels / Ausgabe 8/2019
Print ISSN: 0910-8327
Elektronische ISSN: 1615-2573
DOI
https://doi.org/10.1007/s00380-019-01356-7

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