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用于基于尿液检测膀胱癌的甲基化标志物:用于膀胱癌诊断和监测的新一代尿液标志物。

Methylation markers for urine-based detection of bladder cancer: the next generation of urinary markers for diagnosis and surveillance of bladder cancer.

作者信息

Reinert Thomas

机构信息

Department of Molecular Medicine, Aarhus University Hospital, 8200 Aarhus N, Denmark.

出版信息

Adv Urol. 2012;2012:503271. doi: 10.1155/2012/503271. Epub 2012 Jun 18.

DOI:10.1155/2012/503271
PMID:22761614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3385670/
Abstract

Cancer of the urinary bladder is the fifth most common neoplasm in the industrialized countries. Diagnosis and surveillance are dependent on invasive evaluation with cystoscopy and to some degree cytology as an adjunct analysis. Nomuscle invasive bladder cancer is characterized by frequent recurrences after resection, and up to 30% will develop an aggressive phenotype. The journey towards a noninvasive test for diagnosing bladder cancer, in order to replace or extend time between cystoscopy, has been ongoing for more than a decade. However, only a handful of tests that aid in clinical decision making are commercially available. Recent reports of DNA methylation in urine specimens highlight a possible clinical use of this marker type, as high sensitivities and specificities have been shown. This paper will focus on the currently available markers NMP22, ImmunoCyt, and UroVysion as well as novel DNA methylation markers for diagnosis and surveillance of bladder cancer.

摘要

膀胱癌是工业化国家中第五大常见肿瘤。诊断和监测依赖于膀胱镜检查这种侵入性评估,在一定程度上还依赖于作为辅助分析的细胞学检查。非肌层浸润性膀胱癌的特点是切除术后频繁复发,高达30%的患者会发展为侵袭性表型。为了替代膀胱镜检查或延长其检查间隔时间,寻找一种用于诊断膀胱癌的非侵入性检测方法的探索已经进行了十多年。然而,目前只有少数有助于临床决策的检测方法可供商业使用。最近关于尿液标本中DNA甲基化的报道突出了这种标志物类型可能的临床应用,因为已显示出高敏感性和特异性。本文将重点介绍目前可用的标志物NMP22、免疫细胞化学检测(ImmunoCyt)和UroVysion,以及用于膀胱癌诊断和监测的新型DNA甲基化标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee44/3385670/de52b6e281fe/AU2012-503271.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee44/3385670/de52b6e281fe/AU2012-503271.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee44/3385670/de52b6e281fe/AU2012-503271.001.jpg

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