Skip to main navigation Skip to search Skip to main content

Unravelling the diagnostic dilemma: A microrna panel of circulating MIR-16 and MIR-877 as a diagnostic classifier for distal bile duct tumors

  • Department of Surgery, 1081 HV, Netherlands
  • Department of Medical Oncology, 1081 HV, Netherlands
  • Laboratory of Experimental Oncology and Radiobiology, 1105 AZ, Netherlands
  • Department of Experimental Surgery, 1105 AZ, Netherlands
  • Department of Pharmaceutics, 314001 Jiaxing, China
  • Department of Pharmaceutics, 3584 CG, Netherlands
  • Department of Pathology, 1105 AZ, Netherlands
  • Cancer Pharmacology Lab, 56017 Pisa, Italy
  • Department of Neurosurgery, 1081 HV, Netherlands
  • Medical Oncology Unit, 43 126 Parma, Italy
  • Department of Pathology, 1081 HV, Netherlands
  • Department of Epidemiology and Biostatistics, 1081 HV, Netherlands

Research output: Contribution to journalArticleAcademicpeer-review

27 Downloads (Pure)

Abstract

Accurate diagnosis of pancreatic head lesions remains challenging as no minimally invasive biomarkers are available to discriminate distal cholangiocarcinoma (CCA) from pancreatic ductal adenocarcinoma (PDAC). The aim of this study is to identify specific circulating microRNAs (miRNAs) to diagnose distal CCA. In the discovery phase, PCR profiling of 752 miRNAs was performed on fourteen patients with distal CCA and age- and sex-matched healthy controls. Candidate miRNAs were selected for evaluation and validation by RT-qPCR in an independent cohort of distal CCA (N = 24), healthy controls (N = 32), benign diseases (N = 20), and PDAC (N = 24). The optimal diagnostic combination of miRNAs was determined by multivariate logistic regression analysis and evaluated by ROC curves with AUC values. The discovery phase revealed 19 significantly dysregulated miRNAs, of which six were validated in the evaluation phase. The validation phase confirmed downregulated miR-16 in patients with distal CCA compared to benign disease or PDAC (P = 0.048 and P = 0.012), while miR-877 was significantly upregulated (P = 0.003 and P = 0.006). This two-miRNA panel was validated as a CCA-specific profile, discriminating distal CCA from benign disease (AUC = 0.90) and from PDAC (AUC = 0.88). In conclusion, the present study identified a two-miRNA panel of downregulated miR-16 and upregulated miR-877 with promising capability to diagnose patients with distal CCA.
Original languageEnglish
Article number1181
JournalCancers
Volume11
Issue number8
DOIs
Publication statusPublished - 1 Aug 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Unravelling the diagnostic dilemma: A microrna panel of circulating MIR-16 and MIR-877 as a diagnostic classifier for distal bile duct tumors'. Together they form a unique fingerprint.

Cite this