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Authors Wu MH, Ye XX, Wang SC, Li QH, Lai YX, Yi YM
Received 26 February 2017
Accepted for publication 18 April 2017
Published 2 June 2017 Volume 2017:10 Pages 2815—2822
DOI https://doi.org/10.2147/OTT.S135664
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Ru Chen
Peer reviewer comments 2
Editor who approved publication: Dr Jianmin Xu
Purpose: MicroRNAs (miRNAs) play important roles in tumorigenesis and metastasis
by regulating genes expression. MiRNA-148b (miR-148b) had been reported to
inhibit tumor progression in some kinds of cancers, but the functions of miR-148b
in nasopharyngeal carcinoma (NPC) remain largely unknown. The aim of this study
was to investigate the functional role of miR-148b in NPC.
Methods: Expression of miR-148b in NPC tissues and cell lines
was detected by quantitative reverse transcription polymerase chain reaction.
MiR-148b was overexpressed in CNE2 and C666-1 cells by miR-148b mimic
transfection. The effects of miR-148b on cell proliferation, migration, and
invasion were determined by colony formation assays, cell viability assays, and
transwell assays. The target gene of miR-148b was investigated by luciferase
assays, and the rescue experiment was performed.
Results: MiR-148b was downregulated in NPC tissues and cell
lines. Ectopic miR-148b expression significantly inhibited proliferation,
migration, and invasion of CNE2 and C666-1 cells. We identified that
metastasis-associated gene 2 (MTA2 ) is a direct
target of miR-148b. Rescue experiment demonstrated that the tumor-suppressive
effects of miR-148b on C666-1 cell were partly reversed by restoration of MTA2
expression. Moreover, miR-148b expression was negatively related to mRNA level
of MTA2 in NPC tissues.
Conclusion: Our findings elucidate that miR-148b negatively
regulates the growth, migration, and invasion of NPC cells, at least in part,
by targeting MTA2. The present study indicates that miR-148b is a potential
therapeutic agent for NPC.
Keywords: miR-148b, metastasis-associated gene
2, proliferation, invasion, nasopharyngeal carcinoma
