已发表论文

长非编码 RNA ZEB2-AS1 通过 miR-6840-3p/PLXNB1 轴促进喉鳞状细胞癌进展

 

Authors Xu Q, Liu H, Yu B, Chen W, Zhai L, Li X, Fang Y

Received 18 April 2019

Accepted for publication 31 July 2019

Published 6 September 2019 Volume 2019:12 Pages 7337—7345

DOI https://doi.org/10.2147/OTT.S212749

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Ms Shreya Arora

Peer reviewer comments 2

Editor who approved publication: Dr Leo Jen-Liang Su

Purpose: To investigate the role of zinc finger Eboxbinding homeobox 2 antisense RNA 1 (ZEB2-AS1) in regulating laryngeal squamous cell carcinoma (LSCC) progression.
Patients and methods: In this retrospective study, we included all patients who underwent a surgical operation at The First Hospital of Qiqihaer City for LSCC. Then, we compared the expression of ZEB2-AS1 in LSCC tissues and paired healthy tissues. Besides, we also performed a series of functional assays, CCK8 assays, colony formation assays, and transwell assays to examine the functions of LSCC cells after knockdown of ZEB2-AS1. Through bioinformatics analysis, we predicted that ZEB2-AS1 binds to miR-6840-3p and targets PLXNB1.
Results: We indicated that the expression of ZEB2-AS1 was higher in LSCC tissues compared to the paired adjacent tissues, and ZEB2-AS1 was also highly expressed in LSCC cell lines. Furthermore, we discovered that ZEB2-AS1 promoted cell proliferation, migration and invasion and was associated with poor prognosis. To find the mechanism, we performed bioinformatics analysis. We identified that ZEB2-AS1 binds to miR-6840-3p and targets PLXNB1. Additionally, miR-6840-3p overexpression or knockdown of PLXNB1 decreased the abilities of cell migration and invasion.
Conclusion: These findings demonstrated that overexpression of ZEB2-AS1 promotes LSCC progression. Overexpression of miR-6840-3p or downregulation of PLXNB1 can abrogate ZEB2-AS1-mediated LSCC malignant development.
Keywords: ZEB2-AS1, LSCC, miR-6840-3p, PLXNB1, migration, invasion




Figure 2 Knockdown of ZEB2-AS1 decreased LSCC cell abilities of progression...