FOXO3a knockdown promotes radioresistance in nasopharyngeal carcinoma by inducing epithelial-mesenchymal transition and the Wnt/β-catenin signaling pathway

被引:56
作者
Luo, Min [2 ]
Wu, Cheng [1 ]
Guo, Ergang [1 ]
Peng, Shan [2 ]
Zhang, Linli [1 ]
Sun, Wei [1 ]
Liu, Dongbo [1 ]
Hu, Guangyuan [1 ]
Hu, Guoqing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Oncol, 1095 Jiefang Rd, Wuhan 430030, Hubei, Peoples R China
[2] Wuhan Univ, Dept Radiat & Med Oncol, Zhongnan Hosp, Wuhan, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
NPC; FOXO3a; Radioresistance; Epithelial-mesenchymal transition; Wnt; EPSTEIN-BARR-VIRUS; BETA-CATENIN; CELLS; SUPPRESSES; RESISTANCE; APOPTOSIS; AUTOPHAGY; PROLIFERATION; CONTRIBUTES; METASTASIS;
D O I
10.1016/j.canlet.2019.04.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations in the forkhead box O 3a (FOXO3a) gene are closely related to the progression of several types of cancers. However, few studies explore the relationship between FOXO3a and nasopharyngeal carcinoma (NPC). Our findings demonstrate that silencing FOXO3a promotes tumor radioresistance of NPC in vitro and in vivo through inducing EMT and activating Wnt/beta-catenin signal pathway. These data establish that FOXO3a can be a novel and reliable NPC marker and a potential therapeutic target against NPC.
引用
收藏
页码:26 / 35
页数:10
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