Polycomb group protein EZH2-mediated E-cadherin repression promotes metastasis of oral tongue squamous cell carcinoma

被引:78
作者
Wang, Cheng [1 ,2 ,3 ]
Liu, Xiqiang [1 ,2 ,3 ]
Chen, Zujian [1 ]
Huang, Hongzhang [2 ,3 ]
Jin, Yi [1 ]
Kolokythas, Antonia [1 ,4 ,5 ]
Wang, Anxun [1 ,6 ]
Dai, Yang [5 ,7 ]
Wong, David T. W. [8 ]
Zhou, Xiaofeng [1 ,5 ,9 ]
机构
[1] Univ Illinois, Coll Dent, Ctr Mol Biol Oral Dis, Chicago, IL 60612 USA
[2] Sun Yat Sen Univ, Dept Oral & Maxillofacial Surg, Guanghua Sch, Guangzhou 510055, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Res Inst Stomatol, Guangzhou 510055, Guangdong, Peoples R China
[4] Univ Illinois, Coll Dent, Dept Oral & Maxillofacial Surg, Chicago, IL 60612 USA
[5] Univ Illinois, UIC Canc Ctr, Grad Coll, Chicago, IL 60612 USA
[6] Sun Yat Sen Univ, Dept Oral & Maxillofacial Surg, Affiliated Hosp 1, Guangzhou 510055, Guangdong, Peoples R China
[7] Univ Illinois, Coll Engn, Bioinformat Program, Dept Bioengn, Chicago, IL 60612 USA
[8] Univ Calif Los Angeles, Sch Dent, Dent Res Inst, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
[9] Univ Illinois, Coll Dent, Dept Periodont, Chicago, IL 60612 USA
关键词
EZH2; E-cadherin; metastasis; prognosis; squamous cell carcinoma; LYMPH-NODE METASTASIS; EZH2; EXPRESSION; INVASION; CANCER;
D O I
10.1002/mc.21848
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
Enhancer of Zeste homolog 2 (EZH2) is a critical component of the polycomb-repressive complex 2 (PRC2) that regulates many essential biological processes, including embryogenesis and many developmental events. The oncogenic role of EZH2 has recently been implicated in several cancer types. In this study, we first confirmed that the over-expression of EZH2 is a frequent event in oral tongue squamous cell carcinoma (OTSCC). We further demonstrated that EZH2 over-expression is correlated with advanced stages of the disease and is associated with lymph node metastasis. Statistical analysis revealed that EZH2 over-expression was correlated with reduced overall survival. Furthermore, over-expression of EZH2 was correlated with reduced expression of tumor suppressor gene E-cadherin. These observations were confirmed in vitro, in which knockdown of EZH2-induced E-cadherin expression and reduced cell migration and invasion. In contrast, ectopic transfection of EZH2 led to reduced E-cadherin expression and enhanced cell migration and invasion. Furthermore, EZH2 may act on cell migration in part by suppressing the E-cadherin expression. Taken together, these data suggest that EZH2 plays major roles in the progression of OTSCC, and may serve as a biomarker or therapeutic target for patients at risk of metastasis. (c) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:229 / 236
页数:8
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