Use of a new generation of capillary electrophoresis to quantify circulating free DNA in non-small cell lung cancer

被引:12
作者
Chiappetta, Caterina [1 ]
Anile, Marco [2 ]
Leopizzi, Martina [1 ]
Venuta, Federico [2 ]
Della Rocca, Carlo [1 ]
机构
[1] Sapienza Univ, Fac Med & Pharm, Dept Medicosurg Sci & Biotechnol, Latina, Italy
[2] Univ Roma La Sapienza, Fac Med & Pharm, Dept Thorac Surg, Rome, Italy
关键词
Circulating free DNA; Non-small cell lung cancer; Early diagnosis; QUANTIFICATION; PLASMA;
D O I
10.1016/j.cca.2013.07.014
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 free DNA (cfDNA) is present in higher concentration in non-small-cell lung cancer (NSCLC) patients than in controls. This study was designed to assess the sensitivity and specificity of Agilent 2100 Bioanalyzer to identify patients with NSCLC and to compare it with quantitative RealTime-PCR (RT-qPCR) assay. 30 NSCLC patients and 26 controls were analyzed. The amount of cfDNA was determined both through quantitative RT-PCR targeting the human beta-actin gene and by Agilent 2100 Bioanalyzer. Performances of the assays were calculated by the receiver operating characteristic (ROC) curves. The mean cfDNA concentration, obtained through the use of Agilent 2100 Bioanalyzer, in NSCLC patients (94.5 ng/mL) was almost twice the concentration detected in controls (42.8 ng/mL) as well as found by RT-qPCR (22.5 ng/mL vs 7.1 ng/mL, p < 0.001). The area under curve of Agilent 2100 Bioanalyzer and RT-PCR showed that there are no statistically significant differences between these tests (p < 0.92). This study shows that Agilent 2100 Bioanalyzer is an effective diagnostic tool to discriminate NSCLC patients from healthy individuals and suggests a new approach for early detection of NSCLC. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:93 / 96
页数:4
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