Screening of exosomal microRNAs from colorectal cancer cells

  • Cillian Clancy
  • , Sonja Khan
  • , Claire L. Glynn
  • , Emma Holian
  • , Peter Dockery
  • , Pierce Lalor
  • , James A.L. Brown
  • , Myles R. Joyce
  • , Michael J. Kerin
  • , Roisin M. Dwyer

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND: Cells release extracellular membrane vesicles including microvesicles known as exosomes. Exosomes contain microRNAs (miRNAs) however the full range within colorectal cancer cell secreted exosomes is unknown. OBJECTIVE: To identify the full range of exosome encapsulated miRNAs secreted from 2 colorectal cancer cell lines and to investigate engineering of exosomes over-expressing miRNAs. METHODS: Exosomes were isolated from HCT-116 and HT-29 cell lines. RNA was extracted from exosomes and microRNA array performed. Cells were engineered to express miR-379 (HCT-116-379) or a non-targeting control (HCT-116-NTC) and functional effects were determined. Exosomes secreted by engineered cells were transferred to recipient cells and the impact examined. RESULTS: Microvesicles 40-100 nm in size secreted by cell lines were visualised and confirmed to express exosomal protein CD63. HT-29 exosomes contained 409 miRNAs, HCT-116 exosomes contained 393, and 338 were common to exosomes from both cell lines. Selected targets were validated. HCT-116-379 cells showed decreased proliferation (12-15% decrease, p < 0.001) and decreased migration (32-86% decrease, p < 0.001) compared to controls. HCT-116-379 exosomes were enriched for miR-379. Confocal microscopy visualised transfer of HCT-116-379 exosomes to recipient cells. CONCLUSIONS: Colorectal cancer cells secrete a large number of miRNAs within exosomes. miR-379 decreases cell proliferation and migration, and miR-379 enriched exosomes can be engineered.

Original languageEnglish
Pages (from-to)427-435
Number of pages9
JournalCancer Biomarkers
Volume17
Issue number4
DOIs
Publication statusPublished - 2017
Externally publishedYes

Keywords

  • Colorectal cancer
  • Exosomes
  • MicroRNAs

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