Abstract | OBJECTIVES: MATERIALS AND METHODS: Two-hundred eight mice consisting of 50 FHIT +/+, 63 FHIT +/- and 95 FHIT -/-, were divided into five treatment groups and followed up for 15 weeks. Mice were treated with freshly prepared solution of 0.1% or 0.01% N-butyl-N-(-4-hydroxybutyl)-nitrosamine (BBN) in their drinking water and rofecoxib was administered in mouse chow at 150 parts per million concentration. Mice were sacrificed, and accurate histological analysis of the bladder was performed. RESULTS:
Rofecoxib treatment significantly reduced the incidence of preneoplastic lesions/ bladder tumors (P = 0.016). Comparing the incidence of neoplastic lesions in mice treated with rofecoxib and BBN (22/56, 39.3%) and mice treated only with BBN (32/57, 56.1%), a protective role of rofecoxib on the BBN tumor induction has been observed (P = 0.024). A similar result (P = 0.002) has been reached observing the incidence of mild and moderate dysplasia in mice treated with a lower concentration of BBN (8/16, 50.0% vs. 20/24, 83.3%).Moreover, as previously observed, a significant increase in neoplastic lesions in the FHIT +/- and FHIT -/- vs. FHIT +/+ mice after BBN treatment has been observed (P = 0.003). CONCLUSIONS: These findings suggest that rofecoxib provides a therapeutic defense against bladder carcinogenesis in our model and confirmed that the FHIT knock-out mouse is a suitable system to study in vivo bladder carcinogenesis.
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Authors | Domenico D'Arca, James LeNoir, Bernadette Wildemore, Fedra Gottardo, Emma Bragantini, Dolores Shupp-Byrne, Nicola Zanesi, Matteo Fassan, Carlo M Croce, Leonard G Gomella, Raffaele Baffa |
Journal | Urologic oncology
(Urol Oncol)
2010 Mar-Apr
Vol. 28
Issue 2
Pg. 189-94
ISSN: 1873-2496 [Electronic] United States |
PMID | 19372053
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2010 Elsevier Inc. All rights reserved. |
Chemical References |
- Antineoplastic Agents
- Cyclooxygenase 2 Inhibitors
- Lactones
- Neoplasm Proteins
- Sulfones
- fragile histidine triad protein
- rofecoxib
- Acid Anhydride Hydrolases
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Topics |
- Acid Anhydride Hydrolases
(deficiency, genetics)
- Animals
- Antineoplastic Agents
(therapeutic use)
- Cyclooxygenase 2 Inhibitors
(therapeutic use)
- Female
- Lactones
(therapeutic use)
- Male
- Mice
- Mice, Knockout
- Neoplasm Proteins
(deficiency, genetics)
- Precancerous Conditions
(prevention & control)
- Sulfones
(therapeutic use)
- Urinary Bladder Neoplasms
(prevention & control)
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