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首页> 外文期刊>Journal of experimental & clinical cancer research : >Clinical significance of protocadherin 8 (PCDH8) promoter methylation in non-muscle invasive bladder cancer
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Clinical significance of protocadherin 8 (PCDH8) promoter methylation in non-muscle invasive bladder cancer

机译:原肌钙蛋白8(PCDH8)启动子甲基化在非肌肉浸润性膀胱癌中的临床意义

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Background PCDH8 is a novel tumor suppressor gene, and frequently inactivated by promoter methylation in human cancers. However, there is little information regarding PCDH8 methylation in non-muscle invasive bladder cancer (NMIBC). The aim of this study was to investigate the methylation status of PCDH8 in NMIBC and its clinical significance. Methods The methylation status of PCDH8 in 233 NMIBC tissues and 43 normal bladder epithelial tissues was examined by methylation-specific PCR (MSP), and then analyzed the correlations between PCDH8 methylation and clinicopatholocial features. Subsequently, Kaplan-Meier survival analysis and Multivariate Cox proportional hazard model analysis was used to investigate the correlation between PCDH8 methylation and prognosis of patients with NMIBC. Results PCDH8 methylation occurred frequently in NMIBC tissues than those in normal bladder epithelial tissues. In addition, PCDH8 methylation significantly correlated with advanced stage, high grade, larger tumor size, tumor recurrence and progression in NMIBC. Kaplan-Meier survival analysis revealed that patients with PCDH8 methylated have shorter recurrence-free survival, progression-free survival and five-year overall survival than patients with PCDH8 unmethylated. Multivariate analysis suggested that PCDH8 methylation was an independent prognostic biomarker for recurrence-free survival, progression-free survival and five-year overall survival simultaneously. Conclusions PCDH8 methylation may be associated with tumor progression and poor prognosis in NMIBC and may be used as a potential biomarker to predict the prognosis of patients with NMIBC.
机译:背景技术PCDH8是一种新型的肿瘤抑制基因,在人类癌症中经常被启动子甲基化灭活。但是,关于非肌肉浸润性膀胱癌(NMIBC)中PCDH8甲基化的信息很少。这项研究的目的是调查NMIBC中PCDH8的甲基化状态及其临床意义。方法采用甲基化特异性PCR(MSP)技术检测233例NMIBC组织和43例正常膀胱上皮组织中PCDH8的甲基化状态,并分析PCDH8甲基化与临床病理特征的相关性。随后,使用Kaplan-Meier生存分析和多变量Cox比例风险模型分析来研究PCDH8甲基化与NMIBC患者预后的相关性。结果NMIBC组织中PCDH8甲基化发生率高于正常膀胱上皮组织。此外,PCDH8甲基化与NMIBC的晚期,高级别,较大的肿瘤大小,肿瘤复发和进展密切相关。 Kaplan-Meier生存分析表明,与未甲基化的PCDH8患者相比,甲基化PCDH8的患者具有更短的无复发生存期,无进展生存期和5年总生存期。多变量分析表明,PCDH8甲基化是无复发生存,无进展生存和五年总体生存的独立预后生物标志物。结论PCDH8甲基化可能与NMIBC的肿瘤进展和不良预后有关,可作为预测NMIBC患者预后的潜在生物标志物。

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