Journal
NATURE
Volume 523, Issue 7559, Pages 177-U82Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nature14581
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Funding
- Cancer Prevention and Research Institute of Texas
- UT MD Anderson Cancer Center
- National Institutes of Health (NIH) [CA-155370, CA-151925, DK 081576]
- Metastasis Research Center at the MD Anderson Cancer Center [P30CA016672]
- NIH/NCI [P30CA016672]
- UT MDACC Khalifa Bin Zayed Al Nahya Foundation
- NIH [P50-CA094056, P30CA16672, P30-CA016672, 5U24-CA126577]
- Institutional Core Grant for High Resolution Electron Microscopy Facility [CA16672]
- Deutsche Forschungsgemeinschaf (DFG)
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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. GPC11 circulating exosomes (crExos) were monitored and isolated using flow cytometry from the serum of patients and mice with cancer. GPC11 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 GPC11 crExos correlate with tumour burden and the survival of pre-and post-surgical patients. GPC11 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. GPC11 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.
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