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Authors Yang J, Ye Z, Mei D, Gu H, Zhang J
Received 13 November 2018
Accepted for publication 4 February 2019
Published 7 May 2019 Volume 2019:11 Pages 4209—4221
DOI https://doi.org/10.2147/CMAR.S194453
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Andrew Yee
Peer reviewer comments 3
Editor who approved publication: Dr Antonella D'Anneo
Background: Long
noncoding RNAs (lncRNAs) are abnormally expressed in various human tumors and
play an important role in multiple tumorigeneses, including pancreatic cancer
(PC).
Materials and methods: The
present study was designed to evaluate the role of lncRNA DLX6-AS1 in
tumorigenesis of PC. The expression of DLX6-AS1 and its effect on
proliferation, apoptosis, migration, and invasion was investigated in vitro.
Its effect on tumor growth and metastasis in vivo and its potential targets
were also examined.
Results: We
observed that DLX6-AS1 was highly expressed in PC tissues and PC cell lines,
and was negatively correlated with the survival of PC patients. We found that
overexpression of DLX6-AS1 promoted proliferation, migration, and invasion of
PC cells, inhibited apoptosis, increased Bcl-2, cyclin D1, and MMP-2
expression, and decreased cleaved caspase 3, p27, and E-cadherin expression in
PC cells. In addition, overexpression of DLX6-AS1 promoted PC growth by
increasing tumor volume and weight and increasing the number of liver and lung
metastatic foci. Knockdown of DLX6-AS1 showed an opposite effect in all the
experiments. miR-497-5p was demonstrated to be a direct target of DLX6-AS1 and
was regulated by DLX6-AS1. We also demonstrated that miR-497-5p targeted FZD4
and FZD6 and decreased their expression. miR-497-5p mimics also decreased the
expression of FZD4, FZD6, and β-catenin; the expression of FZD4 or FZD6 was
reversed by the overexpression of vectors FZD4 or FZD6, respectively, while the
expression of β-catenin was reversed by either vector. Finally, the effect of
DLX6-AS1 on proliferation, cell cycle, migration, invasion, and apoptosis of
cells and expression of FZD4, FZD6, and β-catenin was neutralized by
overexpression of vectors of miR-497-5p, FZD4, or FZD6, totally or partially.
Conclusion: Collectively,
these findings suggested that DLX6-AS1/miR-497-5p/FZD4/FZD6/Wnt/β-catenin
signaling pathway is involved in the pathogenesis of PC, and DLX6-AS1 could be
a potential biomarker and target for PC treatment.
Keywords: pancreatic
cancer, DLX6-AS1, long noncoding RNAs, miR-497-5p, FZD4
