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Comparative pathology of dog and human prostate cancer.

Authors :
Ryman-Tubb T
Lothion-Roy JH
Metzler VM
Harris AE
Robinson BD
Rizvanov AA
Jeyapalan JN
James VH
England G
Rutland CS
Persson JL
Kenner L
Rubin MA
Mongan NP
de Brot S
Source :
Veterinary medicine and science [Vet Med Sci] 2022 Jan; Vol. 8 (1), pp. 110-120. Date of Electronic Publication: 2021 Oct 10.
Publication Year :
2022

Abstract

Though relatively rare in dogs, prostate cancer (PCa) is the most common non-cutaneous cancer in men. Human and canine prostate glands share many functional, anatomical and physiological features. Due to these similarities, canine PCa has been proposed as a model for PCa in men. PCa is typically androgen-dependent at diagnosis in men and for this reason, androgen deprivation therapies (ADT) are important treatments for advanced PCa in men. In contrast, there is some evidence that PCa is diagnosed more commonly in castrate dogs, at which point, limited therapeutic options are available. In men, a major limitation of current ADT is that progression to a lethal and incurable form of PCa, termed castrate-resistant prostate cancer (CRPC), is common. There is, therefore, an urgent need for a better understanding of the mechanism of PCa initiation and progression to CRPC to enable the development of novel therapeutic approaches. This review focuses on the functional, physiological, endocrine and histopathological similarities and differences in the prostate gland of these species. In particular, we focus on common physiological roles for androgen signalling in the prostate of men and dogs, we review the short- and longer-term effects of castration on PCa incidence and progression in the dog and relate how this knowledge may be relevant to understanding the mechanisms of CRPC in men.<br /> (© 2021 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
2053-1095
Volume :
8
Issue :
1
Database :
MEDLINE
Journal :
Veterinary medicine and science
Publication Type :
Academic Journal
Accession number :
34628719
Full Text :
https://doi.org/10.1002/vms3.642