Upregulation of COX-1 and COX-2 in nasal polyps in cystic fibrosis
- PMID: 16517580
- PMCID: PMC2104672
- DOI: 10.1136/thx.2004.039842
Upregulation of COX-1 and COX-2 in nasal polyps in cystic fibrosis
Abstract
Background: Since abnormalities in prostanoid metabolism occur in the lower airway of patients with cystic fibrosis (CF), it is likely that they could also be detected in the nose.
Methods: The degree of mRNA and protein expression of cyclo-oxygenase (COX) enzymes 1 (COX-1) and 2 (COX-2) was examined using quantitative reverse competitive polymerase chain reaction (RT-PCR) and Western blot analysis in the nasal polyps from 10 patients with CF, nasal polyps from 10 non-CF patients and 11 nasal mucosa specimens. The results are presented as 10(6) cDNA molecules/mug total RNA and the densitometric ratio between protein and beta-actin.
Results: COX-1 mRNA levels were significantly higher in CF nasal polyps (median 2.34, 25-75th percentiles 1.6-3.2) than in the nasal mucosa (0.78, 0.11-1.21), while there was no difference with non-CF nasal polyps (1.11, 0.80-3.15). COX-1 protein levels were significantly higher in CF nasal polyps (3.63, 2.71-4.27) than in nasal mucosa (1.55, 0.66-2.33) and non-CF nasal polyps (2.19, 1.72-3.68). COX-2 mRNA was significantly higher in CF nasal polyps (3.34, 2.42-7.05) than in nasal mucosa (1.69, 0.19-3.50). No differences were found in COX-2 mRNA expression between CF and non-CF polyps (1.38, 0.12-6.07). COX-2 protein levels were also significantly higher in CF nasal polyps (0.23, 0.04-0.34) than in non-CF nasal polyps (0.011, 0.009-0.016) or nasal mucosa (0.014, 0.014-0.016).
Conclusions: Upregulation in the expression of COX-1 and COX-2 could explain the high production of prostanoids reported in CF. These findings raise questions regarding the potential use of selective or non-selective COX-2 non-steroidal anti-inflammatory treatment in CF.
Conflict of interest statement
Competing interests: none declared.
Comment in
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COX-2: a link between airway inflammation and disordered chloride secretion in cystic fibrosis?Thorax. 2006 Jul;61(7):552-3. doi: 10.1136/thx.2006.060293. Thorax. 2006. PMID: 16807387 Free PMC article.
References
-
- Davis P B, Druman M, Konstan M W. Cystic fibrosis: state of the art. Am J Respir Crit Care Med 19961541229–1256. - PubMed
-
- Isaacson G, Yanagisawa E. Cystic fibrosis and sinusitis. Ear Nose Throat J 199877886–888. - PubMed
-
- Hadfield P J, Rowe‐Jones J M, Mackay I S. The prevalence of nasal polyps in adults with cystic fibrosis. Clin Otolaryngol 20002519–22. - PubMed
-
- Konstan M W, Berger M. Current understanding of the inflammatory process in cystic fibrosis: onset and etiology. Pediatr Pulmonol 199724137–142. - PubMed
-
- Kahn T Z, Wagener J S, Bost T.et al Early pulmonary inflammation in infants with cystic fibrosis. Am J Respir Crit Care Med 1995111075–1082. - PubMed
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