Abstract

Cancer alters cell metabolism. How these changes are manifested in the metabolite cargo of cancer-derived extracellular vesicles (EVs) remains poorly understood. To explore these changes, EVs from prostate, cutaneous T-cell lymphoma (CTCL), colon cancer cell lines, and control EVs from their noncancerous counterparts were isolated by differential ultracentrifugation and analyzed by nanoparticle tracking analysis (NTA), electron microscopy (EM), Western blotting, and liquid chromatography-mass spectrometry (LC-MS). Although minor differences between the cancerous and non-cancerous cell-derived EVs were observed by NTA and Western blotting, the largest differences were detected in their metabolite cargo. Compared to EVs from noncancerous cells, cancer EVs contained elevated levels of soluble metabolites, e.g., amino acids and B vitamins. Two metabolites, proline and succinate, were elevated in the EV samples of all three cancer types. In addition, folate and creatinine were elevated in the EVs from prostate and CTCL cancer cell lines. In conclusion, we present the first evidence in vitro that the altered metabolism of different cancer cells is reflected in common metabolite changes in their EVs. These results warrant further studies on the significance and usability of this metabolic fingerprint in cancer.
Translated title of the contributionSyöpä muuttaa solunulkoisten vesikkelien metabolista sormenjälkeä
Original languageEnglish
Article number3292
JournalCancers
Volume12
Issue number11
Number of pages18
ISSN2072-6694
DOIs
Publication statusPublished - 6 Nov 2020
MoE publication typeA1 Journal article-refereed

Fields of Science

  • 1182 Biochemistry, cell and molecular biology
  • extracellular vesicles
  • cancer metabolism
  • cutaneous T-cell lymphoma
  • prostate cancer
  • colon cancer
  • ONE-CARBON METABOLISM
  • T-CELL LYMPHOMA
  • SERUM CREATININE
  • PROLINE METABOLISM
  • BIOMARKERS
  • HALLMARKS
  • RISK

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