Barták Barbara Kinga, Márkus Eszter, Kalmár Alexandra, Galamb Orsolya, Szigeti Krisztina, Nagy Zsófia Brigitta, Zsigrai Sára, Tulassay Zsolt, Dank Magdolna, Igaz Péter, Molnár Béla
II. Belgyógyászati Klinika, Molekuláris Gasztroenterológia Laboratórium, Semmelweis Egyetem, Általános Orvostudományi Kar Budapest, Szentkirályi u 46., 1088.
Molekuláris Medicina Kutatócsoport, Magyar Tudományos Akadémia Budapest.
Orv Hetil. 2019 Jul;160(30):1167-1177. doi: 10.1556/650.2019.31486.
The incidence and mortality of colorectal cancer (CRC) are considerably high in Central European countries, it is the second most common cancer in both men and women in Hungary with 10,000 newly registered patients per year. These data indicate the necessity of new screening methods that are more comfortable for patients, hence the compliance can be increased. Cell-free DNA (cfDNA) level in blood is elevated in certain physiological conditions, such as pregnancy or high physical activity. Furthermore, cfDNA concentration alterations can also be detected in some pathological processes; increased cfDNA amount was observed in autoimmune and inflammatory diseases, as well as in various cancers including CRC. Numerous studies about origin, function, and mechanism of cfDNA can be found in the scientific literature. In this review, we aimed to describe the quantitative and qualitative changes of cfDNA, to present its functions, and to provide an overview of the available diagnostic applications for CRC. CfDNA can be released to the circulatory system apoptosis, necrosis or by direct secretions by living cells. In cancer patients, cfDNA can originate from healthy and cancer cells, hence genetic ( mutations in ) and epigenetic ( methylation in ) alterations of tumor cells can be examined in cfDNA fraction. Several high-throughput, sensitive and even automated methods are available providing opportunity to perform standardized sample preparation and to analyse biomarker candidates quantitatively. These enhancements can help to develop alternative screening methods that can be easily integrated into the clinical practice and can contribute to early cancer detection. Orv Hetil. 2019; 160(30): 1167-1177.
在中欧国家,结直肠癌(CRC)的发病率和死亡率相当高,在匈牙利,它是男性和女性中第二大常见癌症,每年有10000名新登记患者。这些数据表明需要新的筛查方法,这些方法对患者来说更舒适,从而可以提高依从性。在某些生理条件下,如怀孕或高强度体育活动,血液中的游离DNA(cfDNA)水平会升高。此外,在一些病理过程中也可以检测到cfDNA浓度的变化;在自身免疫性和炎症性疾病以及包括CRC在内的各种癌症中都观察到cfDNA量增加。在科学文献中可以找到许多关于cfDNA的起源、功能和机制的研究。在本综述中,我们旨在描述cfDNA的定量和定性变化,介绍其功能,并概述CRC可用的诊断应用。CfDNA可以通过细胞凋亡、坏死或活细胞的直接分泌释放到循环系统中。在癌症患者中,cfDNA可以来源于健康细胞和癌细胞,因此可以在cfDNA片段中检测肿瘤细胞的基因( 中的突变)和表观遗传( 中的甲基化)改变。有几种高通量、灵敏甚至自动化的方法,提供了进行标准化样品制备和定量分析生物标志物候选物的机会。这些改进有助于开发可轻松融入临床实践并有助于早期癌症检测的替代筛查方法。《匈牙利医学周报》。2019年;160(30):1167 - 1177。