TEL2 suppresses metastasis by down-regulating SERPINE1 in nasopharyngeal carcinoma

被引:37
|
作者
Sang, Yi [1 ,2 ]
Chen, Ming-yuan [1 ]
Luo, Donghua [1 ]
Zhang, Ru-Hua [1 ]
Wang, Li [1 ]
Li, Mei [1 ]
Luo, Rongzhen [1 ]
Qian, Chao-Nan [1 ]
Shao, Jian-Yong [1 ]
Zeng, Yi-Xin [1 ]
Kang, Tiebang [1 ]
机构
[1] Sun Yat Sen Univ, State Key Lab Oncol South China, Collaborat Innovat Ctr Canc Med, Ctr Canc, Guangzhou 510275, Guangdong, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 3, Nanchang Key Lab Canc Pathogenesis & Translat Res, Nanchang, Peoples R China
关键词
nasopharyngeal carcinoma; metastasis; TEL2; SERPINE1; PLASMINOGEN-ACTIVATOR INHIBITOR-1; EPITHELIAL-MESENCHYMAL TRANSITION; ETS TRANSCRIPTION FACTOR; BREAST-CANCER; TUMOR-SUPPRESSOR; PAI-1; EXPRESSION; RADIOTHERAPY; BINDING; SNAIL; P53;
D O I
10.18632/oncotarget.5074
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis is the major cause of treatment failure in patients with nasopharyngeal carcinoma (NPC). However, the molecular mechanisms of NPC metastasis are poorly understood. Here, using our customized gene microarray containing all of the known human transcription factors and the current markers for epithelial-mesenchymal transition, we report that TEL2 was down-regulated in highly metastatic NPC cells and the metastatic tissues in lymph node. Mechanistically, TEL2 inhibits the cell migration and invasion in vitro and metastasis in vivo by releasing its direct suppression on the SERPINE1 promoter in NPC. Consistently, an inverse correlation was observed between the protein levels of TEL2 and SERPINE1 using clinical NPC samples. Collectively, we have provided the first evidence that TEL2 plays a key role in NPC metastasis by directly down-regulating SERPINE1, and that this novel axis of TEL2 / SERPINE1 may be valuable to develop new strategies for treating NPC patients with metastasis.
引用
收藏
页码:29240 / 29253
页数:14
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