Long noncoding RNA TSLNC8 enhances pancreatic cancer aggressiveness by regulating CTNNB1 expression via association with HuR

被引：18

作者：

Chai, Wei ^{[1
]}

Liu, Ruhai ^{[1
]}

Li, Fengshan ^{[1
]}

Zhang, Zhiquan ^{[1
]}

Lei, Bao ^{[1
]}

机构：

[1] Cangzhou Cent Hosp, Dept Gen Surg 1, 16 Xinhua West Rd, Cangzhou 061000, Hebei, Peoples R China

来源：

HUMAN CELL | 2021年 / 34卷 / 01期

关键词：

HuR; mRNA stability; Posttranscriptional regulation; wnt/beta-catenin signaling pathway; BETA-CATENIN; CELL-PROLIFERATION; INVASION; INTERACTS; TARGET; LNCRNA;

D O I：

10.1007/s13577-020-00429-4

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Pancreatic cancer (PC) is one of the most lethal malignancies worldwide. Tumor suppressor long noncoding RNA on chromosome 8p12 (TSLNC8) is a newly identified long noncoding RNA (lncRNA) and play an important role in human cancers. However, the function and molecular mechanism of TSLNC8 in PC progression remain to be elucidated. Our results showed a significant increase of TSLNC8 expression in PC tissues and cell lines. Upregulation of TSLNC8 expression in PC tissues was closely correlated with TNM stage, distant and lymph node metastasis, and poor prognosis of PC patients. Functional experiments demonstrated that TSLNC8 promoted PC cells proliferation and invasion in vitro, and enhanced PC growth and metastasis in vivo. Mechanistically, TSLNC8 associated with HuR, promoted the binding of HuR with CTNNB1 mRNA and increased the stability of CTNNB1 mRNA, thus activating WNT/beta-catenin signaling pathway. Taken together, our present study revealed that oncogenic lncRNA TSLNC8 positively regulate PC growth and metastasis via HuR-mediated mRNA stability of CTNNB1, extending the understanding of PC pathogenesis regulated by lncRNAs.

引用

页码：165 / 176

页数：12

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