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Impact of PSA testing on secondary care costs in England and Wales: estimates from the Cluster randomised triAl of PSA testing for Prostate cancer (CAP)

Abstract:
Prostate cancer is the most common non-cutaneous cancer among men in the UK, causing significant health and economic burdens. Diagnosis and risk prognostication can be challenging due to the genetic and clinical heterogeneity of prostate cancer as well as uncertainties in our knowledge of the underlying biology and natural history of disease development. Urinary extracellular vesicles (EVs) are microscopic, lipid bilayer defined particles released by cells that carry a variety of molecular cargoes including nucleic acids, proteins and other molecules. Urine is a plentiful source of prostate-derived EVs. In this narrative review, we summarise the evidence on the function of urinary EVs and their applications in the evolving field of prostate cancer diagnostics and active surveillance. EVs are implicated in the development of all hallmarks of prostate cancer, and this knowledge has been applied to the development of multiple diagnostic tests, which are largely based on RNA and miRNA. Common gene probes included in multi-probe tests include PCA3 and ERG, and the miRNAs miR-21 and miR-141. The next decade will likely bring further improvements in the diagnostic accuracy of biomarkers as well as insights into molecular biological mechanisms of action that can be translated into opportunities in precision uro-oncology
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12913-023-09503-7
Publication website:
https://ueaeprints.uea.ac.uk/95055/1/cancers_16_01717.pdf

Authors

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Role:
Author
ORCID:
0000-0001-8962-2428
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Role:
Author
ORCID:
0000-0003-2575-387X
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Role:
Author
ORCID:
0000-0001-7696-3661
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Role:
Author
ORCID:
0000-0002-6488-5472
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Role:
Author
ORCID:
0000-0002-6033-5086


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Funder identifier:
10.13039/501100000289
Grant:
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432
C11043/A4286, C18281/A8145, C18281/A11326, C18281/A15064 and C18281/A24432


Publisher:
BioMed Central
Journal:
BMC Health Services Research More from this journal
Volume:
23
Issue:
1
Pages:
610-610
Article number:
610
Publication date:
2023-06-09
DOI:
EISSN:
1472-6963
ISSN:
1472-6963


Language:
English
Keywords:
Pubs id:
1470528
Local pid:
pubs:1470528
Source identifiers:
W4380082862
Deposit date:
2026-05-08
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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