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Overexpression of ubiquitin-specific protease 22 predicts poor survival in patients with early-stage non-small cell lung cancer

机译:泛素特异性蛋白酶22的过表达预示了早期非小细胞肺癌患者的不良生存

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Ubiquitin-specific protease 22 (USP22), a novel ubiquitin hydrolase, has been implicated in oncogenesis and cancer progression in various types of human cancer. However, the clinical significance of USP22 expression in non-small cell lung cancer (NSCLC) has not been determined. In the present study, USP22 messenger RNA (mRNA) and protein levels were analyzed by quantitative real-time polymerase chain reaction (PCR) and western blot analysis in 30 cases of NSCLC and in corresponding non-tumor tissue samples. Furthermore, immunohistochemistry was performed to detect USP22 protein expression in 86 primary tumor tissues derived from clinically annotated NSCLC cases at stage I-II. In our analysis we found that both USP22 mRNA and protein levels in NSCLC tissues were significantly higher than those in corresponding non-tumor tissues and that there was a significant correlation between the expression of USP22 mRNA and protein (P=0.000, κ=0.732). In addition, a high-level of USP22 expression was observed in 53.3% (39 out of 86) cases and it was correlated with large tumor size (P=0.029) and lymph node metastasis (P=0.026). Patients with tumors displaying a high-level of USP22 expression showed significantly shorter survival (P=0.006, log-rank test). Importantly, multivariate analysis showed that high USP22 protein expression was an independent prognostic factor for NSCLC patients (P=0.003). In sum, our data suggest that USP22 plays an important role in NSCLC progression at the early stage, and that overexpression of USP22 in tumor tissues could be used as a potential prognostic marker for patients with early clinical stage of NSCLC.
机译:泛素特异性蛋白酶22(USP22)是一种新型的泛素水解酶,与多种类型的人类癌症的致癌作用和癌症进展有关。但是,USP22表达在非小细胞肺癌(NSCLC)中的临床意义尚未确定。在本研究中,通过定量实时聚合酶链反应(PCR)和蛋白质印迹分析对30例NSCLC和相应的非肿瘤组织样本中的USP22信使RNA(mRNA)和蛋白质水平进行了分析。此外,在I-II期进行免疫组织化学检测USP22蛋白在86例临床注释的NSCLC病例来源的原发性肿瘤组织中的表达。在我们的分析中,我们发现NSCLC组织中USP22 mRNA和蛋白水平均显着高于相应的非肿瘤组织,并且USP22 mRNA和蛋白的表达之间存在显着相关性(P = 0.000,κ= 0.732) 。此外,在53.3%(86个病例中的39个)病例中观察到了高水平的USP22表达,它与大的肿瘤大小(P = 0.029)和淋巴结转移(P = 0.026)相关。患有高水平USP22表达的肿瘤患者生存期明显缩短(P = 0.006,对数秩检验)。重要的是,多变量分析表明,USP22蛋白的高表达是NSCLC患者的独立预后因素(P = 0.003)。总之,我们的数据表明,USP22在NSCLC的早期发展中起着重要作用,并且在肿瘤组织中过表达USP22可以作为NSCLC早期临床患者的潜在预后指标。

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