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A Long Noncoding RNA Activated by TGF-β promotes the invasion-metastasis cascade in hepatocellular carcinoma

机译:TGF-β激活的长非编码RNA促进肝细胞癌的侵袭转移级联反应

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摘要

The role of TGF-β-induced epithelial-mesenchymal transition (EMT) in cancer cell dissemination is well established, but the involvement of lncRNAs in TGF-β signaling is still unknown. In this study, we observed that the lncRNA-activated by TGF-β (lncRNA-ATB) was upregulated in hepatocellular carcinoma (HCC) metastases and associated with poor prognosis. lncRNA-ATB upregulated ZEB1 and ZEB2 by competitively binding the miR-200 family and then induced EMT and invasion. In addition, lncRNA-ATB promoted organ colonization of disseminated tumor cells by binding IL-11 mRNA, autocrine induction of IL-11, and triggering STAT3 signaling. Globally, lncRNA-ATB promotes the invasion-metastasis cascade. Thus, these findings suggest that lncRNA-ATB, a mediator of TGF-β signaling, could predispose HCC patients to metastases and may serve as a potential target for antimetastatic therapies.
机译:TGF-β诱导的上皮-间质转化(EMT)在癌细胞扩散中的作用已被充分确立,但是lncRNAs在TGF-β信号传导中的参与仍然未知。在这项研究中,我们观察到TGF-β激活的lncRNA(lncRNA-ATB)在肝细胞癌(HCC)转移中上调,并与不良预后相关。 lncRNA-ATB通过竞争性结合miR-200家族而上调ZEB1和ZEB2,然后诱导EMT和侵袭。此外,lncRNA-ATB通过结合IL-11 mRNA,自分泌诱导IL-11和触发STAT3信号传导,促进了已扩散肿瘤细胞的器官定植。在全球范围内,lncRNA-ATB促进侵袭转移级联反应。因此,这些发现表明,lncRNA-ATB是TGF-β信号传导的介体,可能使HCC患者易于转移,并可能成为抗转移疗法的潜在靶标。

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