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Overexpression of ubiquitin specific peptidase 14 predicts unfavorable prognosis in esophageal squamous cell carcinoma

机译:泛素特异性肽酶14的过表达预测食管鳞状细胞癌的预后不良

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Abstract BackgroundUbiquitin specific peptidase 14 (USP14), a deubiquitinating enzyme, has been documented as a key element to regulate the proteolysis function of proteasomes and an attractive therapeutic target for several cancers. Herein, we elucidate the role of USP14 in predicting the prognosis of patients with esophageal squamous cell carcinoma (ESCC). Methods USP14 expression was detected in ESCC tissues and matched adjacent non-tumorous tissues by quantitative real-time reverse transcription-PCR and immunohistochemistry. Kaplan–Meier survival analysis was used to assess the correlation between USP14 expression and prognosis in ESCC patients. Univariate and multivariate analysis was conducted with a Cox proportional hazards model to determine whether USP14 is an independent prognostic factor. ResultOverexpression of USP14 was observed in approximately 60% of tested ESCC samples compared to their paired non-tumor esophageal tissues at both RNA and protein levels, and was significantly associated with distant metastasis ( P =?0.001). Kaplan–Meier analysis showed that USP14 overexpression was related to poorer overall patient survival. Univariate and multivariate analyses demonstrated that USP14 was an independent risk factor for overall survival. ConclusionThe findings in this study suggest that USP14 could be used as a potential prognostic marker for ESCC patients.
机译:摘要背景已证明泛素特异性肽酶14(USP14)是一种去泛素化酶,是调节蛋白酶体蛋白水解功能的关键元素,也是多种癌症的诱人治疗靶标。在本文中,我们阐明了USP14在预测食管鳞状细胞癌(ESCC)患者预后中的作用。方法采用实时定量RT-PCR和免疫组化方法在ESCC组织及与之相匹配的非肿瘤组织中检测USP14的表达。 Kaplan–Meier生存分析用于评估USP14表达与ESCC患者预后之间的相关性。使用Cox比例风险模型进行单因素和多因素分析,以确定USP14是否为独立的预后因素。结果在RNA和蛋白质水平上,与配对的非肿瘤食管组织相比,在约60%的ESCC样本中观察到USP14的过表达,并且与远处转移显着相关(P = 0.001)。 Kaplan–Meier分析表明,USP14过表达与总体患者生存期较差有关。单因素和多因素分析表明,USP14是整体生存的独立危险因素。结论本研究发现USP14可作为ESCC患者的潜在预后标志物。

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