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尿液中用于膀胱癌诊断的双基因甲基化标志。

A two-gene methylation signature for the diagnosis of bladder cancer in urine.

机构信息

Amsterdam UMC, Vrije Universiteit Amsterdam, Urology, Cancer Center Amsterdam, Amsterdam, The Netherlands.

Amsterdam UMC, Vrije Universiteit Amsterdam, Pathology, Cancer Center Amsterdam, Amsterdam, The Netherlands.

出版信息

Epigenomics. 2019 Feb;11(3):337-347. doi: 10.2217/epi-2018-0094. Epub 2019 Feb 1.

DOI:10.2217/epi-2018-0094
PMID:30706728
Abstract

AIM

To analyze the potential of 14 cancer-associated genes, including six miRNAs, for bladder cancer (BC) diagnosis in urine.

PATIENTS & METHODS: DNA methylation levels of 14 genes were analyzed in urine of 72 BC patients and 75 healthy controls using quantitative methylation-specific PCR. Multivariate logistic regression analysis was used to determine an optimal marker panel.

RESULTS

Ten genes were significantly hypermethylated in BC patients. The GHSR/MAL combination showed the best diagnostic performance, reaching a sensitivity of 92% (95% CI: 86-99) and a specificity of 85% (95% CI: 76-94).

CONCLUSION

We identified a novel two-gene panel with a high diagnostic accuracy for BC that can be applied in a noninvasive, urine-based test.

摘要

目的

分析 14 个癌症相关基因(包括 6 个 miRNA)在尿液中用于膀胱癌(BC)诊断的潜力。

患者与方法

采用定量甲基化特异性 PCR 分析 72 例 BC 患者和 75 例健康对照者尿液中 14 个基因的 DNA 甲基化水平。采用多变量逻辑回归分析确定最佳标志物组合。

结果

10 个基因在 BC 患者中呈显著高甲基化。GHSR/MAL 组合的诊断性能最佳,其敏感性为 92%(95%CI:86-99),特异性为 85%(95%CI:76-94)。

结论

我们鉴定了一个新的两基因组合,其用于 BC 的诊断准确性高,可应用于非侵入性、基于尿液的检测。

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