Plieskatt Jordan, Rinaldi Gabriel, Feng Yanjun, Peng Jin, Easley Samantha, Jia Xinying, Potriquet Jeremy, Pairojkul Chawalit, Bhudhisawasdi Vajarabhongsa, Sripa Banchob, Brindley Paul J, Bethony Jeffrey, Mulvenna Jason
Department of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, DC, 20037, USA.
Research Center for Neglected Diseases of Poverty, School of Medicine and Health Sciences, George Washington University, Washington, DC, 20037, USA.
BMC Cancer. 2015 Apr 23;15:309. doi: 10.1186/s12885-015-1270-5.
Intrahepatic cholangiocarcinoma (ICC) is a highly aggressive tumor of the bile duct, and a significant public health problem in East Asia, where it is associated with infection by the parasite Opisthorchis viverrini. ICC is often detected at an advanced stage and with a poor prognosis, making a biomarker for early detection a priority.
We have comprehensively profiled miRNA expression levels in ICC tumor tissue using small RNA-Seq and validated these profiles using quantitative PCR on matched plasma samples.
Distinct miRNA profiles were associated with increasing histological differentiation of ICC tumor tissue. We also observed that histologically normal tissue adjacent to ICC tumor displayed miRNA expression profiles more similar to tumor than liver tissue from healthy donors. In plasma samples, an eight-miRNA signature associated with ICC, regardless of the degree of histological differentiation of its matched tissue, forming the basis of a circulating miRNA-based biomarker for ICC.
The association of unique miRNA profiles with different ICC subtypes suggests the involvement of specific miRNAs during ICC tumor progression. In plasma, an eight-miRNA signature associated with ICC could form the foundation of an accessible (plasma-based) miRNA-based biomarker for the early detection of ICC.
肝内胆管癌(ICC)是一种侵袭性很强的胆管肿瘤,在东亚地区是一个重大的公共卫生问题,该地区ICC与华支睾吸虫感染相关。ICC常常在晚期才被发现,预后较差,因此早期检测的生物标志物成为当务之急。
我们使用小RNA测序全面分析了ICC肿瘤组织中的miRNA表达水平,并通过对匹配的血浆样本进行定量PCR验证了这些分析结果。
不同的miRNA谱与ICC肿瘤组织组织学分化程度增加相关。我们还观察到,ICC肿瘤旁的组织学正常组织显示出的miRNA表达谱比健康供体的肝组织更类似于肿瘤组织。在血浆样本中,一个与ICC相关的八miRNA特征,与其匹配组织的组织学分化程度无关,构成了基于循环miRNA的ICC生物标志物的基础。
独特的miRNA谱与不同ICC亚型之间的关联表明特定miRNA参与了ICC肿瘤进展过程。在血浆中,与ICC相关的八miRNA特征可为基于血浆的早期检测ICC的可获取性(基于血浆的)miRNA生物标志物奠定基础。