4.8 Article

miRNA Profiling of Magnetic Nanopore-Isolated Extracellular Vesicles for the Diagnosis of Pancreatic Cancer

Journal

CANCER RESEARCH
Volume 78, Issue 13, Pages 3688-3697

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-17-3703

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Funding

  1. Pennsylvania Department of Health Commonwealth Universal Research Enhancement Program
  2. NIH [1R21CA182336-01A1, R01-CA169123, F31-CA177163-01A1, F32CA196120, R01CA207643]
  3. Pancreatic Cancer Action Network Translational Research Award
  4. Abramson Cancer Center Pancreatic Translational Center of Excellence
  5. Penn Center for Molecular Studies in Digestive and Liver Diseases from the National Institute of Diabetes and Digestive and Kidney Diseases [P30-DK050306]
  6. American Cancer Society - CEOs Against Cancer - CA Division Research Scholar Grant [RSG-15-227-01-CSM]
  7. USAMRMC Award from the US Department of Defense [W81XWH-15-1-0457]
  8. NATIONAL CANCER INSTITUTE [R01CA207643, R21CA182336, R01CA169123, F32CA196120, F31CA177163] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK050306] Funding Source: NIH RePORTER

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Improved diagnostics for pancreatic ductal adenocarcinoma (PDAC) to detect the disease at earlier, curative stages and to guide treatments is crucial to progress against this disease. The development of a liquid biopsy for PDAC has proven challenging due to the sparsity and variable phenotypic expression of circulating biomarkers. Here we report methods we developed for isolating specific subsets of extracellular vesicles (EV) from plasma using a novel magnetic nanopore capture technique. In addition, we present a workflow for identifying EV miRNA biomarkers using RNA sequencing and machine-learning algorithms, which we used in combination to classify distinct cancer states. Applying this approach to a mouse model of PDAC, we identified a biomarker panel of 11 EV miRNAs that could distinguish mice with PDAC from either healthy mice or those with precancerous lesions in a training set of n = 27 mice and a user-blinded validation set of n = 57 mice (88% accuracy in a three-way classification). These results provide strong proof-of-concept support for the feasibility of using EV miRNA profiling and machine learning for liquid biopsy. Significance: These findings present a panel of extracellular vesicle miRNA blood-based biomarkers that can detect pancreatic cancer at a precancerous stage in a transgenic mousemodel. (C) 2018 AACR.

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