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Hsa_circ_0005379 regulates malignant behavior of oral squamous cell carcinoma through the EGFR pathway.

Authors :
Su, Wen
Wang, Yufan
Wang, Feng
Sun, Shuai
Li, Minghua
Shen, Yuehong
Yang, Hongyu
Source :
BMC Cancer; 4/29/2019, Vol. 19 Issue 1, p1-13, 13p, 5 Color Photographs, 1 Black and White Photograph, 1 Chart, 2 Graphs
Publication Year :
2019

Abstract

<bold>Background: </bold>Oral squamous cell carcinoma (OSCC) is an oral and maxillofacial malignancy with a high incidence worldwide. Accumulating evidence indicates that circular RNAs (circRNAs) play a vital role in modulating tumor development. However, the mechanism of circRNA action in human OSCC remains largely unknown.<bold>Methods: </bold>By using high-throughput transcriptome sequencing technology, we conducted a comprehensive study of circRNAs in human OSCC. The effect of circRNA hsa_circ_0005379 on OSCC tissues and cell lines was monitored by qRT-PCR, Transwell assay, flow cytometry, and western blot analysis. Xenograft mouse models were used to assess tumor growth and animal survival.<bold>Results: </bold>We found that circRNA hsa_circ_0005379 expression is significantly lower in OSCC tissue compared to paired non-cancerous matched tissue and is associated with tumor size and differentiation. Overexpression of hsa_circ_0005379 effectively inhibits migration, invasion, and proliferation of OSCC cells in vitro and suppresses OSCC growth in nude mice in vivo. Mechanistic studies revealed that hsa_circ_0005379 may be involved in the regulation of the epidermal growth factor receptor (EGFR) pathway. Furthermore, we found that high expression of hsa_circ_0005379 could significantly enhance the sensitivity of OSCC to the cetuximab drug.<bold>Conclusions: </bold>Our findings provide evidence that hsa_circ_0005379 regulates OSCC malignancy and may be a new therapeutic target for OSCC treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712407
Volume :
19
Issue :
1
Database :
Complementary Index
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
136161023
Full Text :
https://doi.org/10.1186/s12885-019-5593-5