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lncRNA FLVCR-AS1 通过靶向 miR381-3p/CCND1 促进骨肉瘤生长
Authors Yang G, He F, Duan H, Shen J, Dong Q
Received 7 May 2019
Accepted for publication 18 August 2019
Published 9 January 2020 Volume 2020:13 Pages 163—172
DOI https://doi.org/10.2147/OTT.S214813
Checked for plagiarism Yes
Review by Single-blind
Peer reviewer comments 2
Editor who approved publication: Dr Sanjay Singh
Purpose: This article reports on FLVCR-AS1 effects on osteosarcoma (OS) growth.
Methods: Tumor tissue and adjacent normal tissue of 48 OS patients were collected. HOS and 143B cells were transfected. Gene expression was examined with qRT-PCR and Western blot. CCK8 assays and cell cloning was performed to measure cell proliferation. Cell cycle and apoptosis were assessed. Luciferase-reporter gene assays and RNA pull-down tests were used to detect targeting relationships between genes.
Results: Prominently higher FLVCR-AS1 expression was found in OS tissue and cells, and was associated with poor prognosis (P < 0.05, P < 0.01, or P < 0.001). Compared with the siCtrl group, 143B and HOS cells of the siFLVCR-AS1 group had significantly lower OD 450 values and clone numbers and obviously higher percentages of cells in the G 1 phase and apoptosis (P < 0.01 or P < 0.001). miR381-3p expression was directly inhibited by FLVCR-AS1, and CCND1 expression was directly suppressed by miR381-3p. Compared with the FLVCR-AS1 group, 143B cells of the FLVCR-AS1+ miR381-3p mimic group and FLVCR-AS1+ siCCND1 group showed remarkably lower OD 450 values and clone numbers obviously higher apoptosis and percentage of cells in the G 1 phase (P < 0.05, P < 0.01, or P < 0.001).
Conclusion: FLVCR-AS1 promoted OS growth by upregulating CCND1 expression via downregulation of miR381-3p.
Keywords: OS, FLVCR-AS1, miR381-3p, CCND1, proliferation, apoptosis
