Syren Pascal, Andersson Roland, Bauden Monika, Ansari Daniel
a Department of Surgery , Clinical Sciences Lund, Lund University and Skåne University Hospital , Lund , Sweden.
Scand J Gastroenterol. 2017 Jun-Jul;52(6-7):668-673. doi: 10.1080/00365521.2017.1301989. Epub 2017 Mar 16.
Pancreatic ductal adenocarcinoma (PDAC) prognosis remains very poor and has only marginally improved during the last decades. Epigenetic alterations have been the focus of many recent studies and offer valuable options for PDAC detection, prognosis and treatment. DNA methylation, histone modifications and microRNA (miR) level changes can be used as biomarkers. These alterations occur early in carcinogenesis and may be specific for PDAC. Additionally, epigenetic alterations can be analyzed from cell-free DNA, free-circulating nucleosomes or shed tumor cells in blood. High-throughput methods are available for miR and DNA methylation level detection. In particular, multiple promising miR level changes have been discovered. No single epigenetic biomarker that offers a sufficient specificity has been discovered yet, but patterns containing multiple independent biomarkers exist.
胰腺导管腺癌(PDAC)的预后仍然很差,在过去几十年中仅有轻微改善。表观遗传改变一直是近期许多研究的重点,并为PDAC的检测、预后和治疗提供了有价值的选择。DNA甲基化、组蛋白修饰和微小RNA(miR)水平变化可作为生物标志物。这些改变在致癌过程早期就会出现,且可能对PDAC具有特异性。此外,可从游离DNA、游离循环核小体或血液中的脱落肿瘤细胞分析表观遗传改变。有高通量方法可用于检测miR和DNA甲基化水平。特别是,已发现多种有前景的miR水平变化。尚未发现具有足够特异性的单一表观遗传生物标志物,但存在包含多个独立生物标志物的模式。