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长链非编码 RNA TUG1 通过与 miR-144 相互作用,激活肝癌中的 JAK2/STAT3 通路,促进增殖、迁移和肿瘤发生。

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

机构信息

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.

出版信息

Int J Biochem Cell Biol. 2018 Aug;101:19-28. doi: 10.1016/j.biocel.2018.05.010. Epub 2018 May 20.

Abstract

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.

摘要

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。

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