Glypican-1 identifies cancer exosomes and detects early pancreatic cancer

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Sonia A. Melo - , University of Texas at Austin, University of Porto (Author)
  • Linda B. Luecke - , University of Texas at Austin (Author)
  • Christoph Kahlert - , Department of Visceral, Thoracic and Vascular Surgery, University of Texas at Austin (Author)
  • Agustin F. Fernandez - , University of Oviedo (Author)
  • Seth T. Gammon - , University of Texas at Austin (Author)
  • Judith Kaye - , University of Texas at Austin (Author)
  • Valerie S. LeBleu - , University of Texas at Austin (Author)
  • Elizabeth A. Mittendorf - , University of Texas at Austin (Author)
  • Juergen Weitz - , University Medicine (Faculty of Medicine and University Hospital), Department of Visceral, Thoracic and Vascular Surgery, TUD Dresden University of Technology (Author)
  • Nuh Rahbari - , Medical Faculty Carl Gustav Carus, Department of Visceral, Thoracic and Vascular Surgery (Author)
  • Christoph Reissfelder - , Medical Faculty Carl Gustav Carus, Department of Visceral, Thoracic and Vascular Surgery (Author)
  • Christian Pilarsky - , Medical Faculty Carl Gustav Carus, Department of Visceral, Thoracic and Vascular Surgery (Author)
  • Mario F. Fraga - , University of Oviedo, Spanish National Research Council (CSIC) (Author)
  • David Piwnica-Worms - , University of Texas at Austin (Author)
  • Raghu Kalluri - , University of Texas at Austin (Author)

Abstract

Exosomes are lipid-bilayer-enclosed extracellular vesicles that contain proteins and nucleic acids. They are secreted by all cells and circulate in the blood. Specific detection and isolation of cancer-cell-derived exosomes in the circulation is currently lacking. Using mass spectrometry analyses, we identify a cell surface proteoglycan, glypican-1 (GPC1), specifically enriched on cancer-cell-derived exosomes. GPC1+ circulating exosomes (crExos) were monitored and isolated using flow cytometry from the serum of patients and mice with cancer. GPC1+ crExos were detected in the serum of patients with pancreatic cancer with absolute specificity and sensitivity, distinguishing healthy subjects and patients with a benign pancreatic disease from patients with early- and late-stage pancreatic cancer. Levels of GPC1+ crExos correlate with tumour burden and the survival of pre- and post-surgical patients. GPC1+ crExos from patients and from mice with spontaneous pancreatic tumours carry specific KRAS mutations, and reliably detect pancreatic intraepithelial lesions in mice despite negative signals by magnetic resonance imaging. GPC1+ crExos may serve as a potential non-invasive diagnostic and screening tool to detect early stages of pancreatic cancer to facilitate possible curative surgical therapy.

Details

Original languageEnglish
Pages (from-to)177-182
Number of pages6
JournalNature
Volume523
Issue number7559
Publication statusPublished - 9 Jul 2015
Peer-reviewedYes

External IDs

PubMed 26106858

Keywords

Sustainable Development Goals

ASJC Scopus subject areas