Long non-coding RNA NEAT1 facilitates pancreatic cancer progression through negative modulation of miR-506-3p

被引:93
作者
Huang, Bo [1 ]
Liu, Chuan [2 ]
Wu, Qiong [1 ]
Zhang, Jing [1 ]
Min, Qinghua [1 ]
Sheng, Tianle [2 ]
Wang, Xiaozhong [1 ]
Zou, Yeqing [2 ]
机构
[1] Nanchang Univ, Affiliated Hosp 2, Dept Clin Lab, 1 Min De Rd, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 2, Jiangxi Prov Key Lab Mol Med, 1 Min De Rd, Nanchang 330006, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic cancer; Cell proliferation; LncRNA NEAT1; miR-506-3p; CELL-PROLIFERATION; KINASE; INVASION; NETWORKS;
D O I
10.1016/j.bbrc.2016.11.120
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Recently, long non-coding RNAs (lncRNAs) have been shown to have critical regulatory roles in tumourigenesis. Increasing evidence has suggested that IncRNA NEAT1 has been implicated in various types of human cancer. However, the potential biological roles and regulatory mechanisms of NEAT1 in pancreatic cancer (PC) remains unclear. Here, we found that the expression level of NEAT1 was higher in PC tissues compared to the corresponding non-tumor tissues. Besides, our findings indicate that high NEAT1 expression level is closely correlated with tumor progression and poor survival in PC patients. Furthermore, we also found that knockdown of NEAT1 remarkably suppressed cell proliferation by inducing cell cycle arrest and apoptosis promotion in PC cells. Moreover, bioinformatics analysis and luciferase reporter assay revealed that NEAT1 directly bound to the miR-506-3p, which has been reported to act as a tumor suppressor in diverse cancers. Additionally, our results confirmed that the tumor-promoting effects of NEAT1 in PC cells is at least partly through negative modulation of miR-506-3p. Overall, our results suggested that NEAT1 functions as an oncogenic IncRNA in PC, which could be a novel diagnostic and therapeutic target for PC. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:828 / 834
页数:7
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