MicroRNA-9 inhibits the proliferation of oral squamous cell carcinoma cells by suppressing expression of CXCR4 via the Wnt/β-catenin signaling pathway

被引:117
|
作者
Yu, T. [1 ]
Liu, K. [1 ]
Wu, Y. [2 ]
Fan, J. [1 ]
Chen, J. [1 ]
Li, C. [1 ]
Yang, Q. [1 ]
Wang, Z. [1 ]
机构
[1] Sichuan Canc Hosp, Dept Head & Neck Oncol Surg, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Coll Stomatol, State Key Lab Oral Dis, Chengdu 610064, Peoples R China
关键词
microRNA-9; CXC chemokine receptor 4; lentivirus; cell proliferation; oral squamous cell carcinoma; wnt/beta-catenin pathway; DOWN-REGULATION; CANCER; MIR-9; MIGRATION; TONGUE; IDENTIFICATION; INVASION; CADHERIN;
D O I
10.1038/onc.2013.448
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aberrant expression of microRNAs (miRNAs) has been involved in the development and progression of malignancy. MicroRNA-9 (miR-9) has been confirmed to be underexpressed in many types of cancers. However, the relationship between miR-9 and the Wnt/beta-catenin signaling pathway in oral squamous cell carcinoma (OSCC) remains largely unknown. Here we showed that the miR-9 was underexpressed in patients with OSCC and several OSCC cell lines. Lentivirus-mediated miR-9 overexpression in highly aggressive (Tca8113 and SCC-9) tumor cells significantly inhibited proliferation of the two cell lines in vitro and in vivo. Furthermore, we found that the CXC chemokine receptor 4 (CXCR4) gene was a direct target of miR-9. RNA interference silencing of CXCR4 proved that miR-9 underexpression led to constitutive activation of beta-catenin through activation of CXCR4 expression in OSCC cells. Finally, we also analyzed the possible relationship between miR-9 and the genes downstream of the Wnt/beta-catenin pathway in OSCC development and progression. These results provide new evidence of miR-9 as a promising tumor gene therapeutic target for OSCC patients.
引用
收藏
页码:5017 / 5027
页数:11
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