LncRNA TUG1 interacting with miR-144 contributes to proliferation, migration and tumorigenesis through activating the JAK2/STAT3 pathway in hepatocellular carcinoma

被引:74
作者
Lv, Jun [1 ]
Kong, Yongkui [2 ]
Gao, Zhiqiang [3 ]
Liv, Yanmin [1 ]
Zhu, Pengfei [4 ]
Yu, Zujian [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Infect Dis, Zhengzhou, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Blood Transfus, Zhengzhou, Henan, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Zhengzhou, Henan, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 1, Dept Clin Lab, Zhengzhou, Henan, Peoples R China
关键词
TUG1; miR-144; The JAK2/STAT3 pathway; Hepatocellular carcinoma; LONG NONCODING RNA; PROMOTES CELL-PROLIFERATION; DOWN-REGULATION; EMERGING ROLE; OSTEOSARCOMA; INVASION; METASTASIS; SUPPRESSES; MICRORNA; CERNA;
D O I
10.1016/j.biocel.2018.05.010
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
Recently, it is reported that taurine upregulated gene 1 (TUG1) participates in the tumor progression by acting as a competing endogenous RNA (ceRNA) of miRNAs. Nonetheless, whether TUG1 could serve as a ceRNA of miR-144 in hepatocellular carcinoma (HCC) progression remains undefined. Here, our results indicated that there was a marked rise in TUG1 expression in HCC tissues and cells, and downregulation of TUG1 hindered proliferation and migration of HCC cells. Additionally, TUG1 was validated to act as a molecular sponge of miR-144. Furthermore, we found that TUG1 interacting with miR-144 contributed to proliferation and migration of HCC cells via activating the JAK2/STAT3 pathway in vitro. Moreover, TUG1 knockdown inhibited HCC tumor growth in vivo through upregulating miR-144 via inactivation of the JAK2/STAT3 pathway. In conclusion, TUG1 interacting with miR-144 contributed to proliferation, migration and tumorigenesis through activation of the JAK2/STAT3 pathway in HCC.
引用
收藏
页码:19 / 28
页数:10
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