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Identification of the NAC1-regulated genes in ovarian cancer

机译:卵巢癌中NAC1调控基因的鉴定

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摘要

Nucleus accumbens-associated protein 1 (NAC1), encoded by the NACC1 gene, is a transcription co-regulator that plays a multifaceted role in promoting tumorigenesis. However, the NAC1-regulated transcriptome has not been comprehensively defined. In this study, we compared the global gene expression profiles of NAC1-overexpressing SKOV3 ovarian cancer cells and NAC1-knockdown SKOV3 cells. We found that NAC1 knockdown was associated with up-regulation of apoptotic genes and down-regulation of genes involved in cell movement, proliferation, Notch signaling, and epithelial-mesenchymal transition. Among NAC1-regulated genes, FOXQ1 was further characterized because it is involved in cell motility and epithelial-mesenchymal transition. NAC1 knockdown decreased FOXQ1 expression and promoter activity. Similarly, inactivation of NAC1 by expression of a dominant-negative construct of NAC1 suppressed FOXQ1 expression. Ectopic expression of NAC1 in NACC1 null cells induced FOXQ1 expression. NAC1 knockdown resulted in decreased cell motility and invasion, whereas constitutive expression of FOXQ1 rescued motility in cells after NAC1 silencing. Moreover, in silico analysis revealed a significant co-up-regulation of NAC1 and FOXQ1 in ovarian carcinoma tissues. On the basis of transcription profiling, we report a group of NAC1-regulated genes that may participate in multiple cancer-related pathways. We further demonstrate that NAC1 is essential and sufficient for activation of FOXQ1 transcription and that the role of NAC1 in cell motility is mediated, at least in part, by FOXQ1.
机译:由NACC1基因编码的伏伏核相关蛋白1(NAC1)是一种转录共调节因子,在促进肿瘤发生中起多方面的作用。但是,NAC1调控的转录组尚未全面定义。在这项研究中,我们比较了NAC1过表达SKOV3卵巢癌细胞和NAC1基因敲除SKOV3细胞的全球基因表达谱。我们发现,NAC1基因敲低与凋亡基因的上调和细胞运动,增殖,Notch信号传导和上皮-间质转化相关基因的下调有关。在NAC1调控的基因中,FOXQ1被进一步表征,因为它参与细胞运动和上皮-间质转化。 NAC1组合式降低FOXQ1表达和启动子活性。同样,通过表达NAC1的显性负性构建体来使NAC1失活会抑制FOXQ1的表达。 NAC1在NACC1空细胞中的异位表达诱导FOXQ1表达。 NAC1敲低导致细胞运动性和侵袭性降低,而NAC1沉默后FOXQ1的组成型表达挽救了细胞的运动性。此外,计算机分析表明,卵巢癌组织中NAC1和FOXQ1有明显的共同上调。在转录分析的基础上,我们报告了一组NAC1调控的基因,它们可能参与多种与癌症相关的途径。我们进一步证明,NAC1对于激活FOXQ1转录是必不可少的,并且足够,并且NAC1在细胞运动中的作用至少部分由FOXQ1介导。

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