Abstract | BACKGROUND/AIM: Human papillomavirus type 16 (HPV16) induces various types of cancer in several locations. Microenvironmental microRNAs ( miRNAs) such as miRNA-146a and miRNA-150 regulate cancer-associated inflammation and are involved in HPV-induced carcinogenesis. We studied the effects of celecoxib on the expression of these two miRNAs in HPV16-induced lesions. MATERIALS AND METHODS: Female transgenic (HPV16+/-) and wild-type (HPV16-/-) mice were administered 75 mg/kg/day celecoxib orally (treatment groups) or placebo (control groups) for four weeks. Skin samples were classified histologically, or used for miRNA analysis by quantitative real-time PCR. RESULTS: HPV16+/- mice showed higher miRNA-146a and miRNA-150 expression levels compared to wild-type animals. Celecoxib further increased miRNA-150 (p<0.05) and miRNA-146a levels in treated animals. Celecoxib-treated HPV16+/- animals also showed reduced incidence of epidermal dysplasia and reduced inflammation, compared to untreated mice. CONCLUSION: In this model, celecoxib may be able to regulate tumour-associated inflammation, through mechanisms involving the regulation of miRNA-146a and miRNA-150.
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Authors | Rui M Gil DA Costa, Rita Araújo, Joana M O Santos, Mara Fernandes, Tiago Neto, Hugo Sousa, Joana Ribeiro, Margarida M S M Bastos, Paula A Oliveira, Diogo Carmo, Fátima Casaca, Sandra Silva, Carlos Lopes, Rui Medeiros |
Journal | Anticancer research
(Anticancer Res)
Vol. 37
Issue 6
Pg. 2913-2918
(06 2017)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 28551628
(Publication Type: Journal Article)
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Copyright | Copyright© 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Cyclooxygenase 2 Inhibitors
- MicroRNAs
- Mirn146 microRNA, mouse
- Mirn150 microRNA, mouse
- Celecoxib
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Topics |
- Animals
- Celecoxib
(pharmacology)
- Cyclooxygenase 2 Inhibitors
(pharmacology)
- Female
- Human papillomavirus 16
(genetics)
- Mice, Transgenic
- MicroRNAs
(metabolism)
- Precancerous Conditions
(genetics, virology)
- Skin
(metabolism, pathology)
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