Park Jong-Lyul, Kim Hyun Ja, Choi Bo Youl, Lee Han-Chul, Jang Hay-Ran, Song Kyu Sang, Noh Seung-Moo, Kim Seon-Young, Han Dong Soo, Kim Yong Sung
Medical Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 305-806, Republic of Korea.
Oncol Lett. 2012 Apr 1;3(4):921-926. doi: 10.3892/ol.2012.592. Epub 2012 Feb 3.
In the present study, an accurate and reproducible method for quantifying cell-free DNA (cfDNA) in human blood was established and tested for its ability to predict gastric cancer in patients. Using 'Alu81-qPCR' to amplify 81-bp Alu DNA sequences, we first estimated the amount of cfDNA in the serum or plasma of 130 patients with gastric cancer to identify which source of cfDNA is more suitable for the biomarker screening of these patients. The results of Alu81-qPCR revealed that the amount of cfDNA in the plasma was low compared with that in the serum, but was found at similar levels among the samples, indicating that the plasma may be a more suitable source of cfDNA for biomarker screening. For the 54 patients with gastric cancer and the 59 age-matched healthy controls, the mean levels of plasma cfDNA were 2.4-fold higher in the patient group compared with the control group, indicating that plasma cfDNA levels may be useful for predicting patients with gastric cancer. The results of our study suggest that Alu81-qPCR is a more reliable method than other techniques, such as the PicoGreen assay, for quantifying cfDNA in human blood, demonstrating the potential to complement current diagnostic procedures for the management of gastric cancer patients.
在本研究中,建立了一种准确且可重复的定量检测人血中游离DNA(cfDNA)的方法,并对其预测患者胃癌的能力进行了测试。使用“Alu81-qPCR”扩增81 bp的Alu DNA序列,我们首先估计了130例胃癌患者血清或血浆中的cfDNA量,以确定哪种cfDNA来源更适合这些患者的生物标志物筛查。Alu81-qPCR结果显示,与血清相比,血浆中的cfDNA量较低,但在样本中处于相似水平,这表明血浆可能是更适合用于生物标志物筛查的cfDNA来源。对于54例胃癌患者和59例年龄匹配的健康对照,患者组血浆cfDNA的平均水平比对照组高2.4倍,这表明血浆cfDNA水平可能有助于预测胃癌患者。我们的研究结果表明,对于定量检测人血中的cfDNA,Alu81-qPCR是一种比其他技术(如PicoGreen检测法)更可靠的方法,显示出补充当前胃癌患者管理诊断程序的潜力。