Abstract | OBJECTIVE: To evaluate the chemopreventive effect of celecoxib, a specific cyclooxegenease-2 (COX-2) inhibitor, on chemically induced breast cancer of rats and its effect on COX-2 expression. METHODS: RESULTS: The incidence of breast cancer in tamoxifen group (48.15%) and celecoxib group (50.00%) were both significantly lower than that in the control group (85.71%; P=0.003 and P=0.004, respectively). The positivity rate of COX-2 expression in celecoxib group (28.57%) was significantly lower than those of tamoxifen group (48.15%) and control group (83.33%; P=0.001 and P=0.035, respectively). The positivity rate of VEGF expression in celecoxib group (42.86%) was significantly lower than that of control group (79.17%, P=0.023), but comparable with that in tamoxifen group (46.15%, P=0.863). CONCLUSION:
Celecoxib can significantly suppress DMBA-induced breast cancer in female rats possibly through down-regulation of COX-2 and VEGF expressions.
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Authors | Hua-feng Kang, Xi-jing Wang, Xiao-xu Liu, Zhi-jun Dai, Feng-jie Xue, Xing-huan Xue |
Journal | Nan fang yi ke da xue xue bao = Journal of Southern Medical University
(Nan Fang Yi Ke Da Xue Xue Bao)
Vol. 26
Issue 11
Pg. 1599-602
(Nov 2006)
ISSN: 1673-4254 [Print] China |
PMID | 17121709
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cyclooxygenase Inhibitors
- Pyrazoles
- Sulfonamides
- Vascular Endothelial Growth Factor A
- Tamoxifen
- 9,10-Dimethyl-1,2-benzanthracene
- Cyclooxygenase 2
- Celecoxib
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Topics |
- 9,10-Dimethyl-1,2-benzanthracene
- Animals
- Celecoxib
- Cyclooxygenase 2
(metabolism)
- Cyclooxygenase Inhibitors
(therapeutic use)
- Down-Regulation
(drug effects)
- Female
- Immunohistochemistry
- Mammary Neoplasms, Experimental
(chemically induced, metabolism, prevention & control)
- Pyrazoles
(therapeutic use)
- Rats
- Rats, Sprague-Dawley
- Sulfonamides
(therapeutic use)
- Tamoxifen
(therapeutic use)
- Treatment Outcome
- Vascular Endothelial Growth Factor A
(metabolism)
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