Cell-free DNA in the blood as a solid tumor biomarker-A critical appraisal of the literature

被引:269
作者
Jung, Klaus [1 ,2 ]
Fleischhacker, Michael [3 ]
Rabien, Anja [1 ]
机构
[1] Univ Hosp Charite, Div Res, Dept Urol, D-10117 Berlin, Germany
[2] Berlin Inst Urol Res, D-10117 Berlin, Germany
[3] Univ Hosp Charite, Dept Hematol & Oncol, D-10117 Berlin, Germany
关键词
Circulating cell-free DNA; Solid cancer; Mutations; Microsatellites; Methylation marker; Genometastasis hypothesis; FREE PLASMA DNA; FREE CIRCULATING DNA; K-RAS MUTATIONS; BREAST-CANCER PATIENTS; FREE SERUM DNA; CPG ISLAND HYPERMETHYLATION; NUCLEIC-ACID CONCENTRATIONS; LUNG-CANCER; PROMOTER HYPERMETHYLATION; PANCREATIC-CANCER;
D O I
10.1016/j.cca.2010.07.032
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Circulating cell-free DNA (cfDNA) has been suggested as a cancer biomarker. Several studies assessed usefulness of quantitative and qualitative tumor-specific alterations of cfDNA, such as DNA strand frequency of mutations, abnormalities of microsatellites, and methylation of genes, as diagnostic, and monitoring markers in cancer patients. Most of the papers that could be evaluated in this review a positive conclusion. However, methodical diversity without the traceability of data and differently and often underpowered studies resulted in divergent results between studies. In addition, the diagnostic sensitivity and specificity of cfDNA alterations temper the effusive hope of novel tumor raising similar issues as those for other tumor markers. To validate the actual clinical validity of various alterations as potential cancer biomarkers in practice for individual tumor types, the main problems of observed uncertainties must be considered in future studies. These include methodical concerning sample collection, processing, and analysis with the traceability of measurement results as the realization of well-designed prospective studies based on power analysis and sample size (C) 2010 Elsevier B.V. All rights
引用
收藏
页码:1611 / 1624
页数:14
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