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左炔诺孕酮通过 lncRNA H19/miR-17/TLR4 信号通路改善子宫腺肌病
Authors Liang N, Zhang W, Wang H, Shi W, Wang L, Ma L
Received 2 February 2020
Accepted for publication 26 June 2020
Published 24 August 2020 Volume 2020:14 Pages 3449—3460
DOI https://doi.org/10.2147/DDDT.S248095
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Jianbo Sun
Purpose: To explore the mechanism of levonorgestrel (LNG)-ameliorating adenomyosis through long non-coding RNA H19 (lncRNA H19)/miR-17/Toll-like receptor 4 (TLR4) pathway.
Patients and Methods: A total of 71 cases of adenomyosis and 54 cases of normal endometrium were sampled. Quantitative polymerase chain reaction (qPCR) was employed to quantify lncRNA H19, miR-17, and TLR4 mRNA, while Western blot (WB) was used to quantify TLR4 protein. Effects of LNG on normal endometrial stromal cells (ESCs) were evaluated. Suppression/over-expression vectors of lncRNA H19, miR-17, and TLR4 were constructed to observe their effects on ESCs.
Results: MiR-17 and TLR4 mRNA were up-regulated and lncRNA H19 was down-regulated in adenomyosis. After LNG treatment, lncRNA H19 was up-regulated while miR-17 and TLR4 were down-regulated. LNG, up-regulation of lncRNA H19, and down-regulation of miR-17 and TLR4 portend increased apoptosis, G1-arrested cells, as well as inhibited inflammation. Dual-luciferase reporter (DLR) assay conformed the targeting relation of lncRNA H19/miR-17/TLR4 pathway.
Conclusion: LNG ameliorates adenomyosis via lncRNA H19/miR-17/TLR4 pathway.
Keywords: adenomyosis, levonorgestrel, lncRNA H19/miR-17/TLR4 pathway
