4.7 Review

Exosomal miRNAs as cancer biomarkers and therapeutic targets

Journal

JOURNAL OF EXTRACELLULAR VESICLES
Volume 5, Issue -, Pages -

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3402/jev.v5.31292

Keywords

microRNA; exosomes; exosome isolation; oncogenesis; tumour microenvironment; cell communication

Categories

Funding

  1. BBSRC [BB/K017462/1, BB/L007096/1]
  2. Cancer Research UK [C19591/A19076]
  3. Cancer Research UK Oxford Centre Development Fund [C38302/A12278]
  4. John Fell Fund, Oxford
  5. Wellcome Trust
  6. CRUK
  7. Urology Foundation
  8. MRC
  9. Biotechnology and Biological Sciences Research Council [BB/L007096/1, BB/K017462/1] Funding Source: researchfish
  10. Cancer Research UK [19076] Funding Source: researchfish
  11. Medical Research Council [1252459, 1530147] Funding Source: researchfish

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Intercommunication between cancer cells and with their surrounding and distant environments is key to the survival, progression and metastasis of the tumour. Exosomes play a role in this communication process. MicroRNA (miRNA) expression is frequently dysregulated in tumour cells and can be reflected by distinct exosomal miRNA (ex-miRNA) profiles isolated from the bodily fluids of cancer patients. Here, the potential of ex-miRNA as a cancer biomarker and therapeutic target is critically analysed. Exosomes are a stable source of miRNA in bodily fluids but, despite a number of methods for exosome extraction and miRNA quantification, their suitability for diagnostics in a clinical setting is questionable. Furthermore, exosomally transferred miRNAs can alter the behaviour of recipient tumour and stromal cells to promote oncogenesis, highlighting a role in cell communication in cancer. However, our incomplete understanding of exosome biogenesis and miRNA loading mechanisms means that strategies to target exosomes or their transferred miRNAs are limited and not specific to tumour cells. Therefore, if ex-miRNA is to be employed in novel non-invasive diagnostic approaches and as a therapeutic target in cancer, two further advances are necessary: in methods to isolate and detect ex-miRNA, and a better understanding of their biogenesis and functions in tumour-cell communication.

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