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Combining Machine Learning and Nanofluidic Technology To Diagnose Pancreatic Cancer Using Exosomes.
Ko, Jina; Bhagwat, Neha; Yee, Stephanie S; Ortiz, Natalia; Sahmoud, Amine; Black, Taylor; Aiello, Nicole M; McKenzie, Lydie; O'Hara, Mark; Redlinger, Colleen; Romeo, Janae; Carpenter, Erica L; Stanger, Ben Z; Issadore, David.
Afiliación
  • Ko J; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Bhagwat N; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Yee SS; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Ortiz N; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Sahmoud A; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Black T; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Aiello NM; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • McKenzie L; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • O'Hara M; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Redlinger C; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Romeo J; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Carpenter EL; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Stanger BZ; Department of Bioengineering and ∥Department of Electrical and Systems Engineering, School of Engineering and Applied Sciences, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
  • Issadore D; Division of Gastroenterology and §Division of Hematology-Oncology, Department of Medicine, Perelman School of Medicine and ⊥Perelman School of Medicine, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.
ACS Nano ; 11(11): 11182-11193, 2017 11 28.
Article en En | MEDLINE | ID: mdl-29019651
ABSTRACT
Circulating exosomes contain a wealth of proteomic and genetic information, presenting an enormous opportunity in cancer diagnostics. While microfluidic approaches have been used to successfully isolate cells from complex samples, scaling these approaches for exosome isolation has been limited by the low throughput and susceptibility to clogging of nanofluidics. Moreover, the analysis of exosomal biomarkers is confounded by substantial heterogeneity between patients and within a tumor itself. To address these challenges, we developed a multichannel nanofluidic system to analyze crude clinical samples. Using this platform, we isolated exosomes from healthy and diseased murine and clinical cohorts, profiled the RNA cargo inside of these exosomes, and applied a machine learning algorithm to generate predictive panels that could identify samples derived from heterogeneous cancer-bearing individuals. Using this approach, we classified cancer and precancer mice from healthy controls, as well as pancreatic cancer patients from healthy controls, in blinded studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Proteómica / Técnicas Analíticas Microfluídicas / Exosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Proteómica / Técnicas Analíticas Microfluídicas / Exosomas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA