De Maio Giulia, Rengucci Claudia, Zoli Wainer, Calistri Daniele
Giulia De Maio, Claudia Rengucci, Wainer Zoli, Daniele Calistri, Biosciences Laboratory, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori IRCCS, Via Piero Maroncelli, 40-47014 Meldola, Italy.
World J Gastroenterol. 2014 Jan 28;20(4):957-67. doi: 10.3748/wjg.v20.i4.957.
In recent years, the need to identify molecular markers characterized by high sensitivity and specificity in detecting and monitoring early and colorectal cancer lesions has increased. Up to now, none of the markers or panels of markers analyzed have met the rigorous standards required of a screening program. The important discovery of circulating nucleic acids in biological fluids has aroused intense scientific interest because of their usefulness in malignant and non malignant diseases. Over time, their yield and stability have been identified and compared with other "standard" biomarkers. The analysis of circulating DNA from blood and stool is a relatively simple and non-invasive procedure, representing a very attractive marker to detect genetic and epigenetic mutations and to monitor disease progression. A correlation between blood and stool biomarkers could also help to enhance currently available diagnostic approaches. However, various processing and analytic problems need to be resolved before such an approach can be applied in clinical practice.
近年来,在检测和监测早期结直肠癌病变方面,识别具有高灵敏度和特异性的分子标志物的需求不断增加。到目前为止,所分析的任何一种标志物或标志物组合都未达到筛查计划所需的严格标准。生物体液中循环核酸的重要发现因其在恶性和非恶性疾病中的用途而引起了强烈的科学兴趣。随着时间的推移,它们的产量和稳定性已被确定,并与其他“标准”生物标志物进行了比较。对血液和粪便中循环DNA的分析是一种相对简单且非侵入性的程序,是检测基因和表观遗传突变以及监测疾病进展的极具吸引力的标志物。血液和粪便生物标志物之间的相关性也有助于加强目前可用的诊断方法。然而,在这种方法应用于临床实践之前,需要解决各种处理和分析问题。