已发表论文

LncRNA DLX6-AS1  通过靶向 miR-27b-3p/GSPT1  轴促进非小细胞肺癌细胞的增殖、侵袭和迁移

 

Authors Sun W, Zhang L, Yan R, Yang Y, Meng X

Received 3 December 2018

Accepted for publication 12 March 2019

Published 22 May 2019 Volume 2019:12 Pages 3945—3954

DOI https://doi.org/10.2147/OTT.S196865

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 2

Editor who approved publication: Dr XuYu Yang

Background: Non-small cell lung cancer (NSCLC) has a significant impact on human health. The aim of this study was to explore the role of long non-coding RNA DLX6-AS1  in the proliferation, migration, and invasion of NSCLC cells.
Methods: The expression of DLX6-AS1  in NSCLC tumor tissues and cell lines was examined by qRT-PCR. The effects of DLX6-AS1  knockdown on cell proliferation, migration, and invasion were assessed by Cell Counting Kit-8, wound healing, and transwell assays, respectively. Bioinformatics analyses, luciferase reporter assays, and RNA pull-down assays were employed to examine the mechanism by which DLX6-AS1  exerted its oncogenesis effects in NSCLC. The anti-tumor effect of silencing DLX6-AS1  in vivo was also evaluated.
Results: DLX6-AS1  was over-expressed in NSCLC tumor tissues and cell lines and its level of expression was found to be associated with tumor size and advanced clinical stage in patients with NSCLC. Downregulation of DLX6-AS1  inhibited cell proliferation, cell clone formation, migration, and invasion of NSCLC cells. DLX6-AS1  was found to interact with miR-27b-3p/GSPT1 . DLX6-AS1  expression was negatively correlated with miR-27b-3p  expression, but positively correlated with GSPT1 expression in NSCLC samples. DLX6-AS1  knockdown also effectively suppressed tumor growth in an in vivo xenograft model.
Conclusion: DLX6-AS1  regulated NSCLC progression by targeting the miR-27b-3p/GSPT1  axis, which may provide novel insights for NSCLC prognosis and therapy.
Keywords: DLX6-AS1 , NSCLC, miR-27b-3p , GSPT1, invasion




Figure 5 DLX6-AS1 promoted tumor growth in vivo. (A) Tumor growth curves were established by...