Tang Bo, Tang Fang, Li Bo, Yuan Shengguang, Xu Qing, Tomlinson Stephen, Jin Junfei, Hu Wei, He Songqing
Department of Hepatobiliary Surgery, Affiliated Hospital of Guilin Medical University, Guilin, Guangxi, People's Republic of China.
Guangxi Key Laboratory of Molecular Medicine in Liver Injury and Repair, Guilin, Guangxi, People's Republic of China.
Oncotarget. 2015 May 20;6(14):12654-67. doi: 10.18632/oncotarget.3705.
Ubiquitin-specific protease 22 (USP22) removes ubiquitin from histones, thus regulating gene transcription. The expression frequency and expression levels of USP22 were significantly higher in hepatocellular carcinoma (HCC) than in normal liver tissues. High USP22 expression in HCC was significantly correlated with clinical stage and tumor grade. Kaplan-Meier analysis showed that elevated USP22 expression predicted poorer overall survival and recurrence-free survival. High USP22 expression was also associated with shortened survival time in patients at advanced tumor stages and with high grade HCC. Multivariate analyses revealed that USP22 expression is an independent prognostic parameter in HCC. These findings provide evidence that high USP22 expression might be important in tumor progression and serves as an independent molecular marker for poor HCC prognosis. Thus, USP22 overexpression identifies patients at high risk and represents a novel therapeutic molecular target for this tumor.
泛素特异性蛋白酶22(USP22)可从组蛋白上去除泛素,从而调节基因转录。USP22在肝细胞癌(HCC)中的表达频率和表达水平显著高于正常肝组织。HCC中USP22的高表达与临床分期和肿瘤分级显著相关。Kaplan-Meier分析表明,USP22表达升高预示着总体生存率和无复发生存率较差。USP22的高表达还与晚期肿瘤患者和高分级HCC患者的生存时间缩短有关。多变量分析显示,USP22表达是HCC的一个独立预后参数。这些发现提供了证据,表明USP22的高表达可能在肿瘤进展中起重要作用,并作为HCC预后不良的一个独立分子标志物。因此,USP22过表达可识别高危患者,并代表了这种肿瘤的一个新的治疗分子靶点。