Department of Infectious Diseases, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, PR China.
Department of Blood Transfusion, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, PR China.
Int J Biochem Cell Biol. 2018 Aug;101:19-28. doi: 10.1016/j.biocel.2018.05.010. Epub 2018 May 20.
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.
最近有报道称,牛磺酸上调基因 1(TUG1)通过作为 microRNA(miRNA)的竞争性内源 RNA(ceRNA)参与肿瘤进展。然而,TUG1 是否可以作为肝细胞癌(HCC)进展中的 miR-144 的 ceRNA 尚不清楚。在这里,我们的结果表明,在 HCC 组织和细胞中 TUG1 的表达明显升高,下调 TUG1 抑制 HCC 细胞的增殖和迁移。此外,TUG1 被证实可作为 miR-144 的分子海绵。此外,我们发现 TUG1 通过在体外激活 JAK2/STAT3 通路与 miR-144 相互作用,促进 HCC 细胞的增殖和迁移。此外,通过通过失活 JAK2/STAT3 通路,TUG1 敲低在上调 miR-144 抑制体内 HCC 肿瘤生长。总之,TUG1 通过激活 JAK2/STAT3 通路与 miR-144 相互作用,促进 HCC 中的增殖、迁移和肿瘤发生。