Does the Addition of Abiraterone to Castration Affect the Reduction in Bone Mineral Density?

Androgen deprivation therapy bone microenvironment bone mineral density micro-computed tomography osteoblasts

Journal

In vivo (Athens, Greece)
ISSN: 1791-7549
Titre abrégé: In Vivo
Pays: Greece
ID NLM: 8806809

Informations de publication

Date de publication:
Historique:
received: 21 08 2020
revised: 10 09 2020
accepted: 14 09 2020
entrez: 4 11 2020
pubmed: 5 11 2020
medline: 22 6 2021
Statut: ppublish

Résumé

The in vivo effect of abiraterone on bone mineral density (BMD) in addition to androgen deprivation therapy was examined using a murine model. The mice were separated into the following groups: control, abiraterone, castration, and castration+abiraterone. The percentage change in the ratio of bone to tissue volume (BV/TV), number of osteoblasts and osteoclasts, and the serum level of bone markers were compared on day 21. The BV/TV ratio of the abiraterone, castration, and castration+abiraterone groups was lower than that of the control group. However, the change in the BV/TV ratio in the castration+abiraterone group was not significantly different from that in the castration group. There was no significant difference in the serum TRAP5b level and the number of osteoclasts and osteoblasts between the castration+abiraterone and the castration groups. The addition of abiraterone to castration did not affect BMD in the murine model.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
The in vivo effect of abiraterone on bone mineral density (BMD) in addition to androgen deprivation therapy was examined using a murine model.
MATERIALS AND METHODS METHODS
The mice were separated into the following groups: control, abiraterone, castration, and castration+abiraterone. The percentage change in the ratio of bone to tissue volume (BV/TV), number of osteoblasts and osteoclasts, and the serum level of bone markers were compared on day 21.
RESULTS RESULTS
The BV/TV ratio of the abiraterone, castration, and castration+abiraterone groups was lower than that of the control group. However, the change in the BV/TV ratio in the castration+abiraterone group was not significantly different from that in the castration group. There was no significant difference in the serum TRAP5b level and the number of osteoclasts and osteoblasts between the castration+abiraterone and the castration groups.
CONCLUSION CONCLUSIONS
The addition of abiraterone to castration did not affect BMD in the murine model.

Identifiants

pubmed: 33144436
pii: 34/6/3291
doi: 10.21873/invivo.12167
pmc: PMC7811634
doi:

Substances chimiques

Androgen Antagonists 0
Androstenes 0
abiraterone G819A456D0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3291-3299

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

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Auteurs

Shiori Nakajima (S)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Takamitsu Inoue (T)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan takmitz@gmail.com takmitz@iuhw.ac.jp.

Mingguo Huang (M)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Koichiro Takayama (K)

Department of Urology, Municipal Yokote Hospital, Akita, Japan.

Soki Kashima (S)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Ryohei Yamamoto (R)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Atsushi Koizumi (A)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Taketoshi Nara (T)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Kazuyuki Numakura (K)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Mitsuru Saito (M)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Shintaro Narita (S)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

Masatomo Miura (M)

Department of Pharmacy, Akita University Hospital, Akita, Japan.

Shigeru Satoh (S)

Center for Kidney Disease and Transplantation, Akita University Hospital, Akita, Japan.

Tomonori Habuchi (T)

Department of Urology, Akita University Graduate School of Medicine, Akita, Japan.

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Classifications MeSH