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RNA interference-mediated USP22 gene silencing promotes human brain glioma apoptosis and induces cell cycle arrest

机译:RNA干扰介导的USP22基因沉默促进人脑神经胶质瘤凋亡并诱导细胞周期停滞

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摘要

Ubiquitin-specific protease 22 (USP22) is a novel tumor stem cell marker that plays a key role in tumorigenesis and cell cycle progression. However, the effect of silencing the USP22 gene on human brain glioma cell growth is not well understood. In the present study, high gene expression of USP22 was identified in human brain glioma cells. In addition, RNA interference technology was used to silence USP22 gene expression in human brain glioma cells. Silencing the USP22 gene was found to effectively inhibit proliferation of human brain glioma cells, resulting in cell apoptosis and cell cycle arrest at the G2/M phase. USP22 silencing was also found to lead to reduced expression of cell cycle proteins, including CDK1, CDK2 and CyclinB1. In summary, in this study the USP22 gene was demonstrated to play a key regulatory role in the growth of human brain glioma cells by affecting progression of apoptosis and the cell cycle.
机译:泛素特异性蛋白酶22(USP22)是一种新型肿瘤干细胞标记,在肿瘤发生和细胞周期进程中起关键作用。但是,使USP22基因沉默对人脑神经胶质瘤细胞生长的影响尚不清楚。在本研究中,在人脑神经胶质瘤细胞中鉴定出USP22的高基因表达。此外,RNA干扰技术被用于沉默人脑神经胶质瘤细胞中USP22基因的表达。发现沉默USP22基因可有效抑制人脑神经胶质瘤细胞的增殖,从而导致细胞凋亡和细胞周期停滞在G2 / M期。还发现USP22沉默导致细胞周期蛋白(包括CDK1,CDK2和CyclinB1)的表达降低。总之,在这项研究中,USP22基因被证明通过影响细胞凋亡的进程和细胞周期,在人脑神经胶质瘤细胞的生长中起着关键的调节作用。

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