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Knockdown of Upregulated Gene 11 (URG11) Inhibits Proliferation, Invasion, and beta-Catenin Expression in Non-Small Cell Lung Cancer Cells

机译:敲低上调基因11(URG11)抑制非小细胞肺癌细胞的增殖,侵袭和β-连环蛋白的表达。

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Upregulated gene 11 (URG11), a new gene upregulated by hepatitis B virus X protein, was found to be involved in the development and progression of several tumors. However, the role of URG11 in human non-small cell lung cancer (NSCLC) has not yet been determined. Therefore, the aim of the present study was to explore the role of URG11 in human NSCLC. Our results found that URG11 was highly expressed in human NSCLC tissues compared with matched normal lung tissues, and higher levels were found in NSCLC cell lines in comparison to the normal lung cell line. Moreover, we also found that knockdown of URG11 significantly inhibited proliferation, migration/invasion of NSCLC cells, as well as suppressed tumor growth in vivo. Furthermore, knockdown of URG11 suppressed the expression of beta-catenin, c-Myc, and cyclin D1 in NSCLC cells. Taken together, the study reported here provided evidence that URG11 downregulation suppresses proliferation, invasion, and beta-catenin expression in NSCLC cells. Thus, URG11 may be a novel potential therapeutic target for NSCLC.
机译:上调基因11(URG11)是一种由乙型肝炎病毒X蛋白上调的新基因,被发现与几种肿瘤的发生和发展有关。但是,尚未确定URG11在人非小细胞肺癌(NSCLC)中的作用。因此,本研究的目的是探讨URG11在人非小细胞肺癌中的作用。我们的结果发现,与匹配的正常肺组织相比,URG11在人NSCLC组织中高表达,并且在NSCLC细胞系中发现的水平高于正常肺细胞系。此外,我们还发现,敲低URG​​11可以显着抑制NSCLC细胞的增殖,迁移/侵袭,并可以抑制体内肿瘤的生长。此外,敲低URG​​11抑制了NSCLC细胞中β-catenin,c-Myc和cyclin D1的表达。综上所述,该研究报告在这里提供了证据,表明URG11下调抑制了NSCLC细胞中的增殖,侵袭和β-catenin表达。因此,URG11可能是NSCLC的新型潜在治疗靶标。

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