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Curcumin inhibits angiogenesis by up-regulation of micro RNA-1275 and micro RNA-1246: a promising therapy for treatment of corneal neovascularization.

Authors :
Bai, Yanhui
Wang, Weiqun
Sun, Guangli
Zhang, Mingchang
Dong, Jingmin
Source :
Cell Proliferation. Dec2016, Vol. 49 Issue 6, p751-762. 12p.
Publication Year :
2016

Abstract

Objective Curcumin (capable of inhibiting angiogenic growth of human umbilical vein endothelial cells [ HUVECs]), can be employed in vitro as a model of pathogenesis of corneal neovascularization ( CRNV). The aim of this study was to explore regulatory mechanisms of micro RNA (miR) levels after curcumin treatment. Materials and methods Expression profiles of miRs in curcumin-treated HUVECs were investigated by miR microassay. Specific mimics and inhibitors of miR-1275 or miR-1246 were transfected into HUVECs. Then, their target genes, vascular endothelial growth factor B ( VEGFB) and nuclear transcription factor kappa B acting protein ( NKAP) were detected by quantitative real-time PCR, Western blotting assay or immunofluorescence assay. Cell proliferation and cell cycle parameters were measured with the help of CCK-8 assay and flow cytometry. Results MiR-1275 and miR-1246 expression levels were up-regulated by curcumin. Administration of the specific mimics and inhibitors of the two miRs led to significant changes in expression of VEGFB and NKAP as well as the indicators related to angiogenesis. Anti-angiogenic effect of curcumin depended on expression patterns of the two miRs in that inhibition of either miR interfered with the effect of curcumin. Furthermore, overexpression of NKAP interrupted effects of curcumin on the cells. Conclusion Collectively, our findings demonstrate that curcumin inhibited HUVEC proliferation by up-regulation of miR-1275 and miR-1246. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09607722
Volume :
49
Issue :
6
Database :
Academic Search Index
Journal :
Cell Proliferation
Publication Type :
Academic Journal
Accession number :
119206670
Full Text :
https://doi.org/10.1111/cpr.12289