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

被引:67
|
作者
Ko, Jina [1 ]
Bhagwat, Neha [2 ]
Black, Taylor [2 ]
Yee, Stephanie S. [3 ]
Na, Young-Ji [4 ]
Fisher, Stephen [5 ]
Kim, Junhyong [5 ,6 ]
Carpenter, Erica L. [3 ]
Stanger, Ben Z. [2 ]
Issadore, David [1 ,7 ,8 ]
机构
[1] Univ Penn, Sch Engn & Appl Sci, Dept Bioengn, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Med, Div Gastroenterol, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Med, Div Hematol Oncol, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Columbia Univ, Coll Phys & Surg, Dept Med, Div Nephrol, New York, NY USA
[5] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Comp & Informat Sci, 200 S 33Rd St, Philadelphia, PA 19104 USA
[7] Univ Penn, Sch Engn & Appl Sci, Dept Elect & Syst Engn, Philadelphia, PA 19104 USA
[8] Univ Penn, Sch Engn & Appl Sci, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
关键词
CIRCULATING TUMOR-CELLS; EXOSOMES; ADENOCARCINOMA; BIOMARKERS; PROTEIN; MICROVESICLES; MICRORNAS; PATHWAYS; PLASMA; BLOOD;
D O I
10.1158/0008-5472.CAN-17-3703
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:3688 / 3697
页数:10
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