Long noncoding RNA HAS2-AS1 promotes tumor progression in glioblastoma via functioning as a competing endogenous RNA

被引:26
|
作者
Zhang, Liqun [1 ]
Wang, Hong [1 ]
Xu, Meijie [1 ,2 ]
Chen, Fangyu [1 ,3 ]
Li, Wenkui [1 ]
Hu, Haotian [1 ]
Yuan, Quan [1 ]
Su, Yue [1 ]
Liu, Xiaoxuan [1 ]
Wuri, Jimusi [1 ]
Yan, Tao [1 ]
机构
[1] Minist Educ, Dept Neurol, Key Lab Postneurotrauma Neurorepair & Regenerat C, Tianjin Neurol Inst, 154 Anshan Rd, Tianjin 300052, Peoples R China
[2] Xiqing Hosp, Dept Neurol, Tianjin, Peoples R China
[3] Langfang Hosp Tradit Chinese Med, Dept Neurol, Langfang, Hebei, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
competing endogenous RNA; globlastoma multiforme; HAS2-AS1; tumorigenesis; CANCER; GLIOMA; PROLIFERATION; EXPRESSION; PATHWAY; STAT1; MIGRATION; INVASION; PRPS1; NEAT1;
D O I
10.1002/jcb.29313
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
Glioblastoma multiforme (GBM) is a refractory tumor with poor prognosis and requires more effective treatment regimens. It has been confirmed that long noncoding RNAs (lncRNAs) substantially regulate various human disease including GBM. However, the biological roles and its underlying molecular mechanisms still need to be further investigated. In this study, the biological function and potential molecular mechanism of lncHAS2-AS1 in GBM were explored. It was discovered that HAS2-AS1 was elevated in glioma tissues and correlated with the prognosis of patients with glioma. Reduction of HAS2-AS1 suppressed the migration and invasion in vitro and in vivo. The transcription factor STAT1 could raise HAS2-AS1 by binding to its promoter region. Besides, HAS2-AS1 could adjust PRPS1 via sponging miR-608 in a direct manner. On the whole, the results of this study evidence that HAS2-AS1 is an oncogene and a potential therapeutic target for GBM.
引用
收藏
页码:661 / 671
页数:11
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