Salvi Samanta, Gurioli Giorgia, Martignano Filippo, Foca Flavia, Gunelli Roberta, Cicchetti Giacomo, De Giorgi Ugo, Zoli Wainer, Calistri Daniele, Casadio Valentina
Biosciences Laboratory, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, Via P. Maroncelli 40, 47014 Meldola, Italy.
Unit of Biostatistics and Clinical Trials, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST), IRCCS, 47014 Meldola, Italy.
Dis Markers. 2015;2015:574120. doi: 10.1155/2015/574120. Epub 2015 Aug 27.
The detection of tumor-specific markers in urine has paved the way for new early noninvasive diagnostic approaches for prostate cancer. We evaluated the DNA integrity in urine supernatant to verify its capacity to discriminate between prostate cancer and benign diseases of the urogenital tract.
A total of 131 individuals were enrolled: 67 prostate cancer patients and 64 patients with benign diseases of the urogenital tract (control group). Prostate-specific antigen (PSA) levels were determined. Urine cell-free (UCF) DNA was isolated and sequences longer than 250 bp corresponding to 3 genes (c-MYC, HER2, and AR) were quantified by Real-Time PCR to assess UCF-DNA integrity.
UCF-DNA was quantifiable in all samples, while UCF-DNA integrity was evaluable in all but 16 samples. Receiver operating characteristic analysis showed an area under the curve of 0.5048 for UCF-DNA integrity and 0.8423 for PSA. Sensitivity was 0.58 and 0.95 for UCF-DNA integrity and PSA, respectively. Specificity was 0.44 and 0.69, respectively.
UCF-DNA integrity showed lower accuracy than PSA and would not seem to be a reliable marker for early prostate cancer diagnosis. Despite this, we believe that UCF-DNA could represent a source of other biomarkers and could detect gene alterations.
尿液中肿瘤特异性标志物的检测为前列腺癌新的早期非侵入性诊断方法铺平了道路。我们评估了尿液上清液中的DNA完整性,以验证其区分前列腺癌和泌尿生殖道良性疾病的能力。
共纳入131名个体:67例前列腺癌患者和64例泌尿生殖道良性疾病患者(对照组)。测定前列腺特异性抗原(PSA)水平。分离尿液游离(UCF)DNA,并通过实时定量PCR对对应于3个基因(c-MYC、HER2和AR)的长度超过250 bp的序列进行定量,以评估UCF-DNA完整性。
所有样本中的UCF-DNA均可定量,而除16个样本外,所有样本中的UCF-DNA完整性均可评估。受试者工作特征分析显示,UCF-DNA完整性的曲线下面积为0.5048,PSA的曲线下面积为0.8423。UCF-DNA完整性和PSA的敏感性分别为0.58和0.95。特异性分别为0.44和0.69。
UCF-DNA完整性的准确性低于PSA,似乎不是早期前列腺癌诊断的可靠标志物。尽管如此,我们认为UCF-DNA可能代表其他生物标志物的来源,并可检测基因改变。