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Cyclooxygenase-2 inhibitor suppresses tumour progression of prostate cancer bone metastases in nude mice.

Authors :
Garcia, Marta
Velez, Roberto
Romagosa, Cleofé
Majem, Blanca
Pedrola, Núria
Olivan, Mireia
Rigau, Marina
Guiu, Marc
Gomis, Roger R.
Morote, Juan
Reventós, Jaume
Doll, Andreas
Source :
BJU International; May2014, Vol. 113 Issue 5b, pE164-E177, 14p
Publication Year :
2014

Abstract

Objective To assess whether celecoxib, a selective cyclooxygenase-2 ( COX-2) inhibitor with anti-cancer properties, has an inhibitory effect on tumour establishment and progression of prostate cancer ( PCa) bone metastases., Materials and Methods PC-3 stable luciferase-expressing cells were injected into male nude mice by intracardiac (i.c.) and intratibial (i.t.) injections, and the effect of celecoxib on bone metastases was then recorded using bioluminescence image analysis., In cases of chemoprevention, mice received 3 mg/kg celecoxib from 1 week before cell implantation until the end of the study, and to test the therapeutic effect, mice received celecoxib 1 week after cell implantation until the end of the study., Tumour tissue samples were histologically examined and COX-2 expression was quantified at the protein level., Results Celecoxib significantly decreased cell viability and the proliferation of human PCa cells in vitro in a dose-dependent manner., Bone metastases were detected after i.c. injection in nude mice., Celecoxib (15 ppm) administered before i.c. injection did not inhibit the cellular metastatic potential, as the numbers of bone metastases were similar in both groups. However, celecoxib did decrease metastatic progression in the osseous environment when cells were injected directly into the tibia ( P < 0.05)., At the protein level, COX-2 expression was significantly decreased in the celecoxib treatment group ( P < 0.01)., Conclusion In a preclinical mice model, celecoxib administered orally at the standard human dose inhibits the progression of established PCa bone metastases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14644096
Volume :
113
Issue :
5b
Database :
Complementary Index
Journal :
BJU International
Publication Type :
Academic Journal
Accession number :
95683468
Full Text :
https://doi.org/10.1111/bju.12503