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NOVA1 acts as an oncogene in melanoma via regulating FOXO3a expression

机译:Nova1通过调节Foxo3a表达作为黑素瘤的癌基因作用

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Increasing studies have suggested that dysregulation of RNA‐binding proteins (RBPs) contributes to cancer progression. Neuro‐oncological ventral antigen 1 (NOVA1) is a novel RBP and plays an important role in tumour development. However, the expression and role of NOVA1 in melanoma remain unknown. In this study, we indicated that NOVA1 expression was up‐regulated in melanoma samples and cell lines. Moreover, we demonstrated that knockdown of NOVA1 suppressed melanoma cell proliferation, migration and invasion in both A375 and A875 cell lines. In addition, we showed that suppressed expression of NOVA1 enhanced forkhead box O3a (FOXO3a) expression while inhibited AKT expression in melanoma cell. Furthermore, we demonstrated that inhibited expression of FoxO3A rescued NOVA1‐mediated cell proliferation, migration and invasion in melanoma cell line A375. These results suggested that NOVA1 acted as an oncogene in the development of melanoma partly through regulating FoxO3A expression.
机译:增加的研究表明RNA结合蛋白(RBPS)的失调有助于癌症进展。神经肿瘤腹侧抗原1(NOVA1)是一种新的RBP,在肿瘤发育中起重要作用。然而,新星瘤在黑素瘤中的表达和作用仍然未知。在这项研究中,我们表明Nova1表达在黑色素瘤样品和细胞系中调节。此外,我们证明Nova1的敲低抑制了A375和A875细胞中的黑色素瘤细胞增殖,迁移和侵袭。此外,我们表明,在黑色素瘤细胞中抑制了Nova1增强的叉头箱O3a(Foxo3a)表达的表达。此外,我们证明了抑制Foxo3a拯救的Nova1介导的细胞增殖,迁移和侵袭在黑素瘤细胞系A375中的表达。这些结果表明,Nova1通过调节FoxO3a表达,成为黑色素瘤的发育中的癌基因。

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