Long noncoding RNA hotair mediated angiogenesis in nasopharyngeal carcinoma by direct and indirect signaling pathways

被引:168
作者
Fu, Wei-ming [2 ]
Lu, Ying-fei [2 ,3 ]
Hu, Bao-guang [4 ]
Liang, Wei-cheng [5 ]
Zhu, Xiao [6 ]
Yang, Hai-di [7 ]
Li, Gang [3 ,8 ]
Zhang, Jin-fang [1 ,3 ,8 ]
机构
[1] S China Univ Technol, Sch Med, Guangzhou 511458, Guangdong, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Adv Technol, Guangzhou 511458, Guangdong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Orthopaed & Traumatol, Shatin, Hong Kong, Peoples R China
[4] Binzhou Med Univ, Affiliated Hosp, Dept Gastrointestinal Surg, Binzhou, Shandong, Peoples R China
[5] Chinese Univ Hong Kong, Fac Med, Sch Biomed Sci, Hong Kong, Hong Kong, Peoples R China
[6] Guangdong Med Coll, Guangdong Prov Key Lab Med Mol Diag, Dong Guan 523808, Peoples R China
[7] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Otolaryngol, Guangzhou 510275, Guangdong, Peoples R China
[8] Chinese Univ Hong Kong, Shenzhen Res Inst, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
hotair; angiogenesis; nasopharyngeal carcinoma; GRP78; REGULATED PROTEIN 78; POOR-PROGNOSIS; HEPATOCELLULAR-CARCINOMA; TUMOR MICROENVIRONMENT; UP-REGULATION; CANCER CELLS; METASTASIS; EXPRESSION; GRP78/BIP; GROWTH;
D O I
10.18632/oncotarget.6731
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Nasopharyngeal carcinoma (NPC), as a unique head and neck cancer type, is particularly prevalent in certain geographic areas such as eastern Asia. Until now, the therapeutic options have been restricted mainly to radiotherapy or chemotherapy. However, the clinical treatment effect remains unsatisfactory even if the combined radio-chemotherapies. Therefore, it is urgently needed to develop effective novel therapies against NPC. In this study, we discovered that lncRNA Hotair was extremely abundant in NPC cells and clinical NPC samples. Further studies showed that Hotair knockdown significantly attenuated both in vitro and in vivo tumor cell growth and angiogenesis. Our study also demonstrated that Hotair promoted angiogenesis through directly activating the transcription of angiogenic factor VEGFA as well as through GRP78-mediated upregulation of VEGFA and Ang2 expression. Therefore, Hotair may serve as a promising diagnostic marker and therapeutic target for NPC patients.
引用
收藏
页码:4712 / 4723
页数:12
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