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NOVA1 acts as an oncogene in melanoma via regulating FOXO3a expression

机译:NOVA1通过调节FOXO3a表达充当黑色素瘤的癌基因

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摘要

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:越来越多的研究表明,RNA结合蛋白(RBP)的失调会导致癌症进展。神经肿瘤腹侧抗原1(NOVA1)是一种新型RBP,在肿瘤发展中起着重要作用。但是,NOVA1在黑色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上调。此外,我们证明敲除NOVA1可抑制A375和A875细胞系中黑色素瘤细胞的增殖,迁移和侵袭。此外,我们表明抑制NOVA1的表达增强了叉头盒O3a(FOXO3a)的表达,同时抑制了黑色素瘤细胞中AKT的表达。此外,我们证明了抑制FoxO3A的表达可以挽救NOVA1介导的黑色素瘤细胞系A375中的细胞增殖,迁移和侵袭。这些结果表明,NOVA1部分通过调节FoxO3A的表达在黑色素瘤的发展中起着致癌基因的作用。

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