SOX9 promotes nasopharyngeal carcinoma cell proliferation, migration and invasion through BMP2 and mTOR signaling

被引:17
|
作者
Xiao, Bin [1 ]
Zhang, Weiyun [1 ]
Kuang, Zhenzhan [1 ]
Lu, Jingrun [2 ]
Li, Weiwei [2 ]
Deng, Chun [2 ]
He, Yongyin [1 ]
Lei, Ting [1 ]
Hao, Wenbo [3 ]
Sun, Zhaohui [1 ]
Li, Linhai [1 ]
机构
[1] Gen Hosp Southern Theatre Command PLA, Dept Lab Med, Guangzhou 510010, Guangdong, Peoples R China
[2] Guizhou Med Univ, Sch Clin Lab Sci, Dept Basic Clin Lab Med, Guiyang, Guizhou, Peoples R China
[3] Southern Med Univ, Sch Lab Med & Biotechnol, Inst Antibody Engn, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
SOX9; BMP2; Nasopharyngeal carcinoma; mTOR; BONE-MORPHOGENETIC PROTEIN-2; EXPRESSION; METASTASIS;
D O I
10.1016/j.gene.2019.144017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
SAY-related high-mobility-group box 9 (SOX9) is a member of the SOX family of transcription factors. Accumulating evidence has shown that SOX9 plays a significant role in various malignancies. However, the role of SOX9 in nasopharyngeal carcinoma (NPC) remains unknown. In the present study, up-regulation of SOX9 was observed in both NPC tissues and different NPC cells. Overexpression of SOX9 promoted NPC cell proliferation, migration and invasion. Conversely, knock down of SOX9 inhibited NPC proliferation, colony formation, migration and invasion. Mechanistically, SOX9 bound directly to the promoter region of BMP2 and increased BMP2 expression. In addition, overexpression of SOX9 activated the mTOR pathway partly through BMP2. Collectively, these results identify a novel role for SOX9 as a potential therapeutic marker for the prevention and treatment of NPC.
引用
收藏
页数:8
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