Hipler Noam Mathias, Thon Cosima, Lehr Konrad, Furnari Manuele, Obst Wilfried, Keitel Verena, Weigt Jochen, Link Alexander
Department of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Gastroenterology Unit, Department of Internal Medicine, Policlinico San Martino-IRCCS Hospital, University of Genoa, 16145 Genoa, Italy.
Cancers (Basel). 2025 Mar 31;17(7):1171. doi: 10.3390/cancers17071171.
BACKGROUND/OBJECTIVES: Obstruction of the biliary duct may be caused by various conditions ranging from chronic inflammation to neoplasia, including cholangiocarcinoma (CCA). While the definite histological diagnosis of intrahepatic lesions is relatively straightforward, the diagnostic workup of biliary duct stenosis can be challenging, despite the availability of novel tools for intraductal diagnosis. This proof-of-principle study aimed to investigate whether microRNAs (miRNAs) from bile duct stents may be used as biomarkers to differentiate between various bile duct diseases.
For this purpose, we included 100 patients with one or more bile duct stents for various reasons, including malignant disease ( = 40), stenosis due to liver transplantation or surgery ( = 60), and cholangitis ( = 42). During endoscopic retrograde cholangiography, the stents were collected, and miRNA analyses were performed to evaluate miR-16, miR-21, and miR-223.
All studied miRNAs were successfully detected from the specimens obtained from the bile duct stents and were comparable in different stents from the same subjects. Following normalization, significant increases in miR-16, -21, and -223 levels were identified in patients with cholangitis compared to specimens from a non-inflammatory cohort. However, when comparing the data from patients in the malignant and non-malignant cohorts, the individual levels of miR-16, miR-21, and miR-223 showed high variation, without reaching a statistically significant difference.
In summary, bile duct stents can be considered as potential sources of intraductal biomarkers, specifically miRNAs. Further profiling and validation analyses are necessary to identify the most appropriate miRNA targets for differentiating bile duct diseases.
背景/目的:胆管梗阻可能由多种情况引起,从慢性炎症到肿瘤形成,包括胆管癌(CCA)。虽然肝内病变的明确组织学诊断相对简单,但胆管狭窄的诊断检查可能具有挑战性,尽管有用于导管内诊断的新工具。这项原理验证研究旨在调查来自胆管支架的微小RNA(miRNA)是否可用作生物标志物以区分各种胆管疾病。
为此,我们纳入了100例因各种原因置入一个或多个胆管支架的患者,包括恶性疾病(n = 40)、肝移植或手术引起的狭窄(n = 60)以及胆管炎(n = 42)。在内镜逆行胆管造影期间,收集支架,并进行miRNA分析以评估miR-16、miR-21和miR-223。
所有研究的miRNA均成功从胆管支架获得的标本中检测到,并且在同一受试者的不同支架中具有可比性。标准化后,与非炎症队列的标本相比,胆管炎患者的miR-16、-21和-223水平显著升高。然而,在比较恶性和非恶性队列患者的数据时,miR-16、miR-21和miR-223的个体水平显示出高度差异,未达到统计学显著差异。
总之,胆管支架可被视为导管内生物标志物的潜在来源,特别是miRNA。需要进一步的分析和验证分析来确定区分胆管疾病的最合适的miRNA靶点。