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泛素特异性肽酶24的变体在肺癌恶性肿瘤中起关键作用。

Variants of ubiquitin-specific peptidase 24 play a crucial role in lung cancer malignancy.

作者信息

Wang Y-C, Wang S-A, Chen P-H, Hsu T-I, Yang W-B, Chuang Y-P, Su W-C, Liaw H-J, Chang W-C, Hung J-J

机构信息

Institute of Basic Medical Sciences, National Cheng Kung University, Tainan, Taiwan.

Institute of Bioinformatics and Biosignal Transduction, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan.

出版信息

Oncogene. 2016 Jul 14;35(28):3669-80. doi: 10.1038/onc.2015.432. Epub 2015 Nov 16.

DOI:10.1038/onc.2015.432
PMID:26568301
Abstract

Ubiquitin is a critical modifier regulating the degradation and function of its target proteins during posttranslational modification. Here we found that ubiquitin-specific peptidase 24 (USP24) is highly expressed in cell lines with enhanced malignancy and in late-stage lung cancer clinical samples. Studying single-nucleotide polymorphisms (SNPs) of USP24 using genomic DNA of lung cancer patients revealed an increase in SNP 7656C/T. When using RNA specimens instead of the genomic DNA of lung cancer patients, we found significant increases in the ratios of variants 930C/T and 7656T/C, suggesting that variants at these two sites are not only caused by the SNP of DNA but also by the RNA editing. USP24-930T and USP24-7656C increase USP24 expression levels by increasing RNA stability. Knocking down USP24 increased Suv39h1 level through a decrease in mouse double-minute 2 homolog levels, thus enhancing lysine-9 methylation of histone H3, and resulting in the prevention of lung cancer malignancy. In conclusion, as USP24 variant analysis revealed a higher ratio of variants in blood specimens of lung cancer patients than that in normal individuals, USP24-930T and USP24-7656C might be useful as diagnostic markers for cancer detection.

摘要

泛素是一种关键的修饰因子,在翻译后修饰过程中调节其靶蛋白的降解和功能。我们发现,泛素特异性肽酶24(USP24)在恶性程度增强的细胞系和晚期肺癌临床样本中高表达。利用肺癌患者的基因组DNA研究USP24的单核苷酸多态性(SNP),发现SNP 7656C/T增加。当使用肺癌患者的RNA样本而非基因组DNA时,我们发现930C/T和7656T/C变体的比例显著增加,这表明这两个位点的变体不仅由DNA的SNP引起,还由RNA编辑引起。USP24-930T和USP24-7656C通过增加RNA稳定性来提高USP24的表达水平。敲低USP24可通过降低小鼠双微体2同源物水平来增加Suv39h1水平,从而增强组蛋白H3的赖氨酸-9甲基化,进而预防肺癌的恶性进展。总之,由于USP24变体分析显示肺癌患者血液样本中的变体比例高于正常个体,USP24-930T和USP24-7656C可能作为癌症检测的诊断标志物。

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