Kadiyska Tanya, Nossikoff Alexander
Tanya Kadiyska, Genetic Medico-Diagnostic Laboratory Genica, Sofia 1463, Bulgaria.
World J Gastroenterol. 2015 Sep 21;21(35):10057-61. doi: 10.3748/wjg.v21.i35.10057.
Colorectal cancer (CRC) is fourth most common cancer in men and third in women worldwide. Developing a diagnostic panel of sensitive and specific biomarkers for the early detection of CRC is recognised as to be crucial for early initial diagnosis, which in turn leads to better long term survival. Most of the research on novel potential CRC biomarkers in the last 2 decades has been focussed on stool DNA analysis. In this paper, we describe the recent advances in non-invasive CRC screening and more specifically in molecular assays for aberrantly methylated BMP3 and NDRG4 promoter regions. In several research papers these markers showed superior rates for sensitivity and specificity in comparison to previously described assays. These tests detected the majority of adenomas ≥ 1 cm in size and the detection rates progressively increased with larger adenomas. The methylation status of the BMP3 and NDRG4 promoters demonstrated effective detection of neoplasms at all sites throughout the colon and was not affected by common clinical variables. Recently, a multitarget stool DNA test consisting of molecular assays for aberrantly methylated BMP3 and NDRG4 promoter regions, mutant KRAS and immunochemical assay for human haemoglobin has been made commercially available and is currently reimbursed in the United States. Although this is the most sensitive non-invasive CRC screening test, there is the need for further research in several areas - establishment of the best timeframe for repeated DNA stool testing; validation of the results in populations outside of North America; usefulness for surveillance and prognosis of patients; cost-effectiveness of DNA stool testing in real-life populations.
结直肠癌(CRC)是全球男性中第四大常见癌症,女性中第三大常见癌症。开发一组用于早期检测CRC的敏感且特异的生物标志物诊断面板,被认为对早期初步诊断至关重要,这进而会带来更好的长期生存率。过去20年中,大多数关于新型潜在CRC生物标志物的研究都集中在粪便DNA分析上。在本文中,我们描述了非侵入性CRC筛查的最新进展,更具体地说是关于异常甲基化的BMP3和NDRG4启动子区域的分子检测。在几篇研究论文中,这些标志物与先前描述的检测方法相比,显示出更高的灵敏度和特异度。这些检测方法能检测出大多数直径≥1 cm的腺瘤,且随着腺瘤增大,检测率逐渐升高。BMP3和NDRG4启动子的甲基化状态证明对整个结肠所有部位的肿瘤都有有效的检测能力,且不受常见临床变量的影响。最近,一种多靶点粪便DNA检测方法已商业化,该方法包括对异常甲基化的BMP3和NDRG4启动子区域的分子检测、KRAS突变检测以及人血红蛋白免疫化学检测,目前在美国已可报销。尽管这是最敏感的非侵入性CRC筛查检测方法,但在几个领域仍需进一步研究——确定重复粪便DNA检测的最佳时间框架;在北美以外人群中验证结果;对患者监测和预后的有用性;在实际人群中粪便DNA检测的成本效益。