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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
